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Volumn 19, Issue 21, 2013, Pages 3884-3930

Current developments of coumarin compounds in medicinal chemistry

Author keywords

Antibacterial; Anticancer; Anticoagulant; Antioxidative; Biological stain; Coumarin; Probe; Supramolecular drug

Indexed keywords

ANALGESIC AGENT; ANTICOAGULANT AGENT; ANTIDEPRESSANT AGENT; ANTIDIABETIC AGENT; ANTIFUNGAL AGENT; ANTIINFECTIVE AGENT; ANTINEOPLASTIC AGENT; ANTIOXIDANT; ANTIPARASITIC AGENT; ANTIPARKINSON AGENT; ANTIVIRUS AGENT; AP 2243; AROMATASE INHIBITOR; BETA SECRETASE INHIBITOR; COUMARIN DERIVATIVE; DIAGNOSTIC AGENT; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; FATTY ACID AMIDASE INHIBITOR; GAMMA LACTONE DERIVATIVE; HEAT SHOCK PROTEIN 90 INHIBITOR; KU 398; MONOAMINE OXIDASE A INHIBITOR; MONOAMINE OXIDASE B INHIBITOR; NEUROPROTECTIVE AGENT; NOOTROPIC AGENT; PIPERIDINE DERIVATIVE; PYRANOCOUMARIN DERIVATIVE; QUATERNARY AMMONIUM DERIVATIVE; TAMOXIFEN; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 84878657077     PISSN: 13816128     EISSN: 18734286     Source Type: Journal    
DOI: 10.2174/1381612811319210013     Document Type: Review
Times cited : (444)

References (428)
  • 3
    • 79961149485 scopus 로고    scopus 로고
    • Coumarin: A plant derived polyphenol with wide biomedical applications
    • Mirunalini S, Krishnaveni M. Coumarin: a plant derived polyphenol with wide biomedical applications. Int J PharmTech Res 2011; 3: 1693-6.
    • (2011) Int J PharmTech Res , vol.3 , pp. 1693-1696
    • Mirunalini, S.1    Krishnaveni, M.2
  • 5
    • 84856221609 scopus 로고    scopus 로고
    • A review on coumarins as acetylcholinesterase inhibitors for Alzheimer's disease
    • Anand P, Singh B, Singh N. A review on coumarins as acetylcholinesterase inhibitors for Alzheimer's disease. Bioorg Med Chem 2012; 20: 1175-80.
    • (2012) Bioorg Med Chem , vol.20 , pp. 1175-1180
    • Anand, P.1    Singh, B.2    Singh, N.3
  • 7
    • 77950643074 scopus 로고    scopus 로고
    • Coumarins: Old compounds with novel promising therapeutic perspectives
    • Riveiro ME, Kimpe ND, Moglioni A, et al. Coumarins: old compounds with novel promising therapeutic perspectives. Curr Med Chem 2010; 17: 1325-38.
    • (2010) Curr Med Chem , vol.17 , pp. 1325-1338
    • Riveiro, M.E.1    Kimpe, N.D.2    Moglioni, A.3
  • 8
    • 70450162772 scopus 로고    scopus 로고
    • The structure and pharmacological functions of coumarins and their derivatives
    • Wu L, Wang X, Xu W, Farzaneh F, Xu R. The structure and pharmacological functions of coumarins and their derivatives. Curr Med Chem 2009; 16: 4236-60.
    • (2009) Curr Med Chem , vol.16 , pp. 4236-4260
    • Wu, L.1    Wang, X.2    Xu, W.3    Farzaneh, F.4    Xu, R.5
  • 9
    • 70349197543 scopus 로고    scopus 로고
    • Biological activity of metal ions complexes of chromones, coumarins and flavones
    • Grazul M, Budzisz E. Biological activity of metal ions complexes of chromones, coumarins and flavones. Coord Chem Rev 2009; 253: 2588-98.
    • (2009) Coord Chem Rev , vol.253 , pp. 2588-2598
    • Grazul, M.1    Budzisz, E.2
  • 10
    • 58949096544 scopus 로고    scopus 로고
    • The use of coumarins as environmentally-sensitive fluorescent probes of heterogeneous inclusion systems
    • Wagner BD. The use of coumarins as environmentally-sensitive fluorescent probes of heterogeneous inclusion systems. Molecules 2009; 14: 210-37.
    • (2009) Molecules , vol.14 , pp. 210-237
    • Wagner, B.D.1
  • 11
    • 60049093579 scopus 로고    scopus 로고
    • Application quantum and physico chemical molecular descriptors utilizing principal components to study mode of anticoagulant activity of pyridyl chromen-2-one derivatives
    • Bhatia MS, Ingale KB, Choudhari PB, Bhatia NM, Sawant RL. Application quantum and physico chemical molecular descriptors utilizing principal components to study mode of anticoagulant activity of pyridyl chromen-2-one derivatives. Bioorg Med Chem 2009; 17: 1654-62.
    • (2009) Bioorg Med Chem , vol.17 , pp. 1654-1662
    • Bhatia, M.S.1    Ingale, K.B.2    Choudhari, P.B.3    Bhatia, N.M.4    Sawant, R.L.5
  • 12
    • 84892441917 scopus 로고    scopus 로고
    • Clinical evaluation and rational use of coumarin anticoagulants
    • Du LP, Zhang GL, Mei D. Clinical evaluation and rational use of coumarin anticoagulants. Eval Anal Drug-use Hosp China 2008; 8: 576-9.
    • (2008) Eval Anal Drug-use Hosp China , vol.8 , pp. 576-579
    • Du, L.P.1    Zhang, G.L.2    Mei, D.3
  • 13
    • 79959780064 scopus 로고    scopus 로고
    • Research progress on application of coumarin and its derivatives
    • Wang H, Lu XM, Yao H, Feng JK, Liu RJ. Research progress on application of coumarin and its derivatives. Chem Ind Times 2009; 23: 40-3.
    • (2009) Chem Ind Times , vol.23 , pp. 40-43
    • Wang, H.1    Lu, X.M.2    Yao, H.3    Feng, J.K.4    Liu, R.J.5
  • 14
    • 77949462773 scopus 로고    scopus 로고
    • Pharmacogenetics of oral anticoagulant therapy
    • Schalekamp T, de Boer A. Pharmacogenetics of oral anticoagulant therapy. Curr Pharm Des 2010; 16: 187-203.
    • (2010) Curr Pharm Des , vol.16 , pp. 187-203
    • Schalekamp, T.1    de Boer, A.2
  • 15
    • 80052935202 scopus 로고    scopus 로고
    • Genotyping for CYP2C9 and VKORC1 alleles by a novel point of care assay with HyBeacon probes
    • Howard R, Leathart JBS, French DJ, et al. Genotyping for CYP2C9 and VKORC1 alleles by a novel point of care assay with HyBeacon probes. Clin Chim Acta 2011; 412: 2063-9.
    • (2011) Clin Chim Acta , vol.412 , pp. 2063-2069
    • Howard, R.1    Leathart, J.B.S.2    French, D.J.3
  • 17
    • 84862798425 scopus 로고    scopus 로고
    • Substrate speci city of acetoxy derivatives of coumarins and quinolones towards calreticulin mediated transacetylation: Investigations on antiplatelet function
    • Kathuria A, Priya N, Chand K, et al. Substrate speci city of acetoxy derivatives of coumarins and quinolones towards calreticulin mediated transacetylation: investigations on antiplatelet function. Bioorg Med Chem 2012; 20: 1624-38.
    • (2012) Bioorg Med Chem , vol.20 , pp. 1624-1638
    • Kathuria, A.1    Priya, N.2    Chand, K.3
  • 18
    • 84855864857 scopus 로고    scopus 로고
    • Calreticulin transacetylase: A novel enzyme-mediated protein acetylation by acetoxy derivatives of 3-alkyl-4-methylcoumarins
    • Jalal S, Chand K, Kathuria A, et al. Calreticulin transacetylase: a novel enzyme-mediated protein acetylation by acetoxy derivatives of 3-alkyl-4-methylcoumarins. Bioorg Chem 2012; 40: 131-6.
    • (2012) Bioorg Chem , vol.40 , pp. 131-136
    • Jalal, S.1    Chand, K.2    Kathuria, A.3
  • 19
    • 84864398367 scopus 로고    scopus 로고
    • Biochemical and pharmacological evaluation of 4-hydroxychromen-2-ones bearing polar C-3 substituents as anticoagulants
    • Mladenović M, Mihailović M, Bogojević D, et al. Biochemical and pharmacological evaluation of 4-hydroxychromen-2-ones bearing polar C-3 substituents as anticoagulants. Eur J Med Chem 2012; 54: 144-58.
    • (2012) Eur J Med Chem , vol.54 , pp. 144-158
    • Mladenović, M.1    Mihailović, M.2    Bogojević, D.3
  • 21
    • 44949161937 scopus 로고    scopus 로고
    • Novel 3-carboxamide-coumarins as potent and selective FXIIa inhibitors
    • Robert S, Bertolla C, Masereel B, Dogné JM, Poche L. Novel 3-carboxamide-coumarins as potent and selective FXIIa inhibitors. J Med Chem 2008; 51: 3077-80.
    • (2008) J Med Chem , vol.51 , pp. 3077-3080
    • Robert, S.1    Bertolla, C.2    Masereel, B.3    Dogné, J.M.4    Poche, L.5
  • 23
    • 84864300783 scopus 로고    scopus 로고
    • Scyllo-inositol, preclinical, and clinical data for Alzheimer's disease
    • Ma K, Thomason LAM, McLaurin J. Scyllo-inositol, preclinical, and clinical data for Alzheimer's disease. Adv Pharmacol 2012; 64: 177-212.
    • (2012) Adv Pharmacol , vol.64 , pp. 177-212
    • Ma, K.1    Thomason, L.A.M.2    McLaurin, J.3
  • 24
    • 84868705553 scopus 로고    scopus 로고
    • "It ain't over 'til it's over"a-the search for treatments and cures for Alzheimer's disease
    • Hargreaves RJ. "It ain't over 'til it's over"a-the search for treatments and cures for Alzheimer's disease. ACS Med Chem Lett 2012; 3: 862-6.
    • (2012) ACS Med Chem Lett , vol.3 , pp. 862-866
    • Hargreaves, R.J.1
  • 25
    • 84866466056 scopus 로고    scopus 로고
    • QSAR applications during last decade on inhibitors of acetylcholinesterase in Alzheimer's disease
    • Wong KY, Duchowicz PR, Mercader AG, Castro EA. QSAR applications during last decade on inhibitors of acetylcholinesterase in Alzheimer's disease. Mini-Rev Med Chem 2012; 12: 936-46.
    • (2012) Mini-Rev Med Chem , vol.12 , pp. 936-946
    • Wong, K.Y.1    Duchowicz, P.R.2    Mercader, A.G.3    Castro, E.A.4
  • 26
    • 84857253918 scopus 로고    scopus 로고
    • 3-Substituted coumarins as dual inhibitors of AChE and MAO for the treatment of Alzheimer's disease
    • Viña D, Matos MJ, Yáñez M, Santana L, Uriarte E. 3-Substituted coumarins as dual inhibitors of AChE and MAO for the treatment of Alzheimer's disease. Med Chem Comm 2012; 3: 213-8.
    • (2012) Med Chem Comm , vol.3 , pp. 213-218
    • Viña, D.1    Matos, M.J.2    Yáñez, M.3    Santana, L.4    Uriarte, E.5
  • 27
    • 50249237889 scopus 로고    scopus 로고
    • Design, synthesis, and acetylcholinesterase inhibitory activity of novel coumarin analogs
    • Zhou X, Wang XB, Wang T, Kong LY. Design, synthesis, and acetylcholinesterase inhibitory activity of novel coumarin analogs. Bioorg Med Chem 2008; 16: 8011-21.
    • (2008) Bioorg Med Chem , vol.16 , pp. 8011-8021
    • Zhou, X.1    Wang, X.B.2    Wang, T.3    Kong, L.Y.4
  • 29
    • 48449093461 scopus 로고    scopus 로고
    • Homo-and hetero-bivalent edrophonium-like ammonium salts as highly potent, dual binding site AChE inhibitors
    • Leonetti F, Catto M, Nicolotti O, et al. Homo-and hetero-bivalent edrophonium-like ammonium salts as highly potent, dual binding site AChE inhibitors. Bioorg Med Chem 2008; 16: 7450-6.
    • (2008) Bioorg Med Chem , vol.16 , pp. 7450-7456
    • Leonetti, F.1    Catto, M.2    Nicolotti, O.3
  • 30
    • 77956413632 scopus 로고    scopus 로고
    • Design, synthesis, and biological evaluation of coumarin derivatives tethered to an edrophonium-like fragment as highly potent and selective dual binding site acetylcholinesterase inhibitors
    • Pisani L, Catto M, Giangreco I, et al. Design, synthesis, and biological evaluation of coumarin derivatives tethered to an edrophonium-like fragment as highly potent and selective dual binding site acetylcholinesterase inhibitors. ChemMedChem 2010; 5: 1616-30.
    • (2010) ChemMedChem , vol.5 , pp. 1616-1630
    • Pisani, L.1    Catto, M.2    Giangreco, I.3
  • 31
    • 77951776829 scopus 로고    scopus 로고
    • Alzheimer's disease: Strategies for disease modification
    • Citron M. Alzheimer's disease: strategies for disease modification. Nat Rev Drug Disc 2010; 9: 387-98.
    • (2010) Nat Rev Drug Disc , vol.9 , pp. 387-398
    • Citron, M.1
  • 33
    • 65649116587 scopus 로고    scopus 로고
    • Chemistry of small molecule inhibitors in self-assembly of Alzheimer's disease related amyloidbeta peptide
    • Torok B, Dasgupta S, Torok M. Chemistry of small molecule inhibitors in self-assembly of Alzheimer's disease related amyloidbeta peptide. Curr Bioact Comp 2008; 4: 159-74.
    • (2008) Curr Bioact Comp , vol.4 , pp. 159-174
    • Torok, B.1    Dasgupta, S.2    Torok, M.3
  • 34
    • 79954426004 scopus 로고    scopus 로고
    • Inhibition of amyloid-β aggregation by coumarin analogs can be manipulated by functionalization of the aromatic center
    • Soto-Ortega DD, Murphy BP, Gonzalez-Velasquez FJ, et al. Inhibition of amyloid-β aggregation by coumarin analogs can be manipulated by functionalization of the aromatic center. Bioorg Med Chem 2011; 19: 2596-602.
    • (2011) Bioorg Med Chem , vol.19 , pp. 2596-2602
    • Soto-Ortega, D.D.1    Murphy, B.P.2    Gonzalez-Velasquez, F.J.3
  • 35
    • 84855775879 scopus 로고    scopus 로고
    • Structure-activity relationships for naturally occurring coumarins as β-secretase inhibitor
    • Marumoto S, Miyazawa M. Structure-activity relationships for naturally occurring coumarins as β-secretase inhibitor. Bioorg Med Chem 2012; 20: 784-8.
    • (2012) Bioorg Med Chem , vol.20 , pp. 784-788
    • Marumoto, S.1    Miyazawa, M.2
  • 36
    • 80052605106 scopus 로고    scopus 로고
    • Bioactivity-guided fractionation for the butyrylcholinesterase inhibitory activity of furanocoumarins from Angelica archangelica L. roots and fruits
    • Wszelaki N, Paradowska K, Jamróz MK, Granica S, Kiss AK. Bioactivity-guided fractionation for the butyrylcholinesterase inhibitory activity of furanocoumarins from Angelica archangelica L. roots and fruits. J Agric Food Chem 2011; 59: 9186-93.
    • (2011) J Agric Food Chem , vol.59 , pp. 9186-9193
    • Wszelaki, N.1    Paradowska, K.2    Jamróz, M.K.3    Granica, S.4    Kiss, A.K.5
  • 37
    • 37549066630 scopus 로고    scopus 로고
    • Multi-target-directed coumarin derivatives: HAChE and BACE1 inhibitors as potential antialzheimer compounds
    • Piazzi L, Cavalli A, Colizzi F, et al. Multi-target-directed coumarin derivatives: hAChE and BACE1 inhibitors as potential antialzheimer compounds. Bioorg Med Chem Lett 2008; 18: 423-6.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 423-426
    • Piazzi, L.1    Cavalli, A.2    Colizzi, F.3
  • 38
    • 84858241256 scopus 로고    scopus 로고
    • The first dual ChE/FAAH inhibitors: New perspectives for Alzheimer's disease
    • Rampa A, Bartolini M, Bisi A, et al. The first dual ChE/FAAH inhibitors: new perspectives for Alzheimer's disease. ACS Med Chem Lett 2012; 3: 182-6.
    • (2012) ACS Med Chem Lett , vol.3 , pp. 182-186
    • Rampa, A.1    Bartolini, M.2    Bisi, A.3
  • 39
    • 80053462390 scopus 로고    scopus 로고
    • Targeting monoamine oxidases with multipotent ligands: An emerging strategy in the search of new drugs against neurodegenerative diseases
    • Pisani L, Catto M, Leonetti F, et al. Targeting monoamine oxidases with multipotent ligands: an emerging strategy in the search of new drugs against neurodegenerative diseases. Curr Med Chem 2011; 18: 4568-87.
    • (2011) Curr Med Chem , vol.18 , pp. 4568-4587
    • Pisani, L.1    Catto, M.2    Leonetti, F.3
  • 40
    • 84871094408 scopus 로고    scopus 로고
    • Recent advances in the multitarget-directed ligands approach for the treatment of Alzheimer's disease
    • Leon R, Garcia AG, Marco-Contelles J. Recent advances in the multitarget-directed ligands approach for the treatment of Alzheimer's disease. Med Res Rev 2013; 33: 139-89.
    • (2013) Med Res Rev , vol.33 , pp. 139-189
    • Leon, R.1    Garcia, A.G.2    Marco-Contelles, J.3
  • 41
    • 84874893498 scopus 로고    scopus 로고
    • Focusing on new monoamine oxidase inhibitors: Differently substituted coumarins as an interesting scaffold
    • Oxford Centre for Innovation Mill Street, Oxford OX2 0JX, UK: Clinical Pub Serv; 1 edition June, in press
    • Matos MJ, Viña D, Vazquez-Rodriguez S, Uriarte E, Santana L. Focusing on new monoamine oxidase inhibitors: differently substituted coumarins as an interesting scaffold. Curr Top Med Chem 2012; in press.
    • (2012) Curr Top Med Chem
    • Matos, M.J.1    Viña, D.2    Vazquez-Rodriguez, S.3    Uriarte, E.4    Santana, L.5
  • 42
    • 66149173641 scopus 로고    scopus 로고
    • Molecular and mechanistic properties of the membrane-bound mitochondrial monoamine oxidases
    • Edmondson DE, Binda C, Wang J, Upadhayay AK, Mattevi A. Molecular and mechanistic properties of the membrane-bound mitochondrial monoamine oxidases. Biochemistry 2009; 48: 4220-30.
    • (2009) Biochemistry , vol.48 , pp. 4220-4230
    • Edmondson, D.E.1    Binda, C.2    Wang, J.3    Upadhayay, A.K.4    Mattevi, A.5
  • 43
    • 51249118269 scopus 로고    scopus 로고
    • Monoamine oxidase inactivation: From pathophysiology to therapeutics
    • Bortolato M, Chen K, Shih JC. Monoamine oxidase inactivation: from pathophysiology to therapeutics. Adv Drug Deliv Rev 2008; 60: 1527-33.
    • (2008) Adv Drug Deliv Rev , vol.60 , pp. 1527-1533
    • Bortolato, M.1    Chen, K.2    Shih, J.C.3
  • 44
    • 65749116833 scopus 로고    scopus 로고
    • A new series of 3-phenylcoumarins as potent and selective MAO-B inhibitors
    • Matos MJ, Viña D, Quezada E, et al. A new series of 3-phenylcoumarins as potent and selective MAO-B inhibitors. Bioorg Med Chem Lett 2009; 19: 3268-70.
    • (2009) Bioorg Med Chem Lett , vol.19 , pp. 3268-3270
    • Matos, M.J.1    Viña, D.2    Quezada, E.3
  • 45
    • 68349155549 scopus 로고    scopus 로고
    • Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors
    • Matos MJ, Viña D, Picciau C, Orallo F, Santana L, Uriarte E. Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors. Bioorg Med Chem Lett 2009; 19: 5053-5.
    • (2009) Bioorg Med Chem Lett , vol.19 , pp. 5053-5055
    • Matos, M.J.1    Viña, D.2    Picciau, C.3    Orallo, F.4    Santana, L.5    Uriarte, E.6
  • 46
    • 80054908624 scopus 로고    scopus 로고
    • Synthesis and study of a series of 3-arylcoumarins as potent and selective monoamine oxidase B inhibitors
    • Matos MJ, Terán C, Pérez-Castillo Y, Uriarte E, Santana L, Viña D. Synthesis and study of a series of 3-arylcoumarins as potent and selective monoamine oxidase B inhibitors. J Med Chem 2011; 54: 7127-37.
    • (2011) J Med Chem , vol.54 , pp. 7127-7137
    • Matos, M.J.1    Terán, C.2    Pérez-Castillo, Y.3    Uriarte, E.4    Santana, L.5    Viña, D.6
  • 49
    • 71049173711 scopus 로고    scopus 로고
    • Discovery of a novel class of potent coumarin monoamine oxidase B inhibitors: Development and biopharmacological profiling of 7-[(3-chlorobenzyl)oxy]-4-[(methylamino)methyl]-2H-chromen-2-one methanesulfonate (NW-1772) as a highly potent, selective, reversible, and orally active monoamine oxidase B inhibitor
    • Pisani L, Muncipinto G, Miscioscia TF, et al. Discovery of a novel class of potent coumarin monoamine oxidase B inhibitors: development and biopharmacological profiling of 7-[(3-chlorobenzyl)oxy]-4-[(methylamino)methyl]-2H-chromen-2-one methanesulfonate (NW-1772) as a highly potent, selective, reversible, and orally active monoamine oxidase B inhibitor. J Med Chem 2009; 52: 6685-706.
    • (2009) J Med Chem , vol.52 , pp. 6685-6706
    • Pisani, L.1    Muncipinto, G.2    Miscioscia, T.F.3
  • 50
    • 80053187018 scopus 로고    scopus 로고
    • Synthesis and selective human monoamine oxidase inhibition of 3-carbonyl, 3-acyl, and 3-carboxyhydrazido coumarin derivatives
    • Secci D, Carradori S, Bolasco A, et al. Synthesis and selective human monoamine oxidase inhibition of 3-carbonyl, 3-acyl, and 3-carboxyhydrazido coumarin derivatives. Eur J Med Chem 2011; 46: 4846-52.
    • (2011) Eur J Med Chem , vol.46 , pp. 4846-4852
    • Secci, D.1    Carradori, S.2    Bolasco, A.3
  • 51
    • 64549137053 scopus 로고    scopus 로고
    • Synthesis, molecular modeling, and selective inhibitory activity against human monoamine oxidases of 3-carboxamido-7-substituted coumarins
    • Chimenti F, Secci D, Bolasco A, et al. Synthesis, molecular modeling, and selective inhibitory activity against human monoamine oxidases of 3-carboxamido-7-substituted coumarins. J Med Chem 2009; 52: 1935-42.
    • (2009) J Med Chem , vol.52 , pp. 1935-1942
    • Chimenti, F.1    Secci, D.2    Bolasco, A.3
  • 52
    • 79952282900 scopus 로고    scopus 로고
    • Synthesis, human monoamine oxidase inhibitory activity and molecular docking studies of 3-heteroarylcoumarin derivatives
    • Delogu G, Picciau C, Ferino G, et al. Synthesis, human monoamine oxidase inhibitory activity and molecular docking studies of 3-heteroarylcoumarin derivatives. Eur J Med Chem 2011; 46: 1147-52.
    • (2011) Eur J Med Chem , vol.46 , pp. 1147-1152
    • Delogu, G.1    Picciau, C.2    Ferino, G.3
  • 53
    • 56249083925 scopus 로고    scopus 로고
    • Quantitative structure activity-relationship and complex network approach to monoamine oxidase A and B inhibitors
    • Santana L, González-Dāaz H, Quezada E, et al. Quantitative structure activity-relationship and complex network approach to monoamine oxidase A and B inhibitors. J Med Chem 2008; 51: 6740-51.
    • (2008) J Med Chem , vol.51 , pp. 6740-6751
    • Santana, L.1    González-Daaz, H.2    Quezada, E.3
  • 54
    • 84868032139 scopus 로고    scopus 로고
    • Fullerenes for cancer diagnosis and therapy: Preparation, biological and clinical perspectives
    • Chen ZY, Mao RQ, Liu Y. Fullerenes for cancer diagnosis and therapy: preparation, biological and clinical perspectives. Curr Drug Metab 2012; 13: 1035-45.
    • (2012) Curr Drug Metab , vol.13 , pp. 1035-1045
    • Chen, Z.Y.1    Mao, R.Q.2    Liu, Y.3
  • 55
    • 53549123007 scopus 로고    scopus 로고
    • Advances in the research of the alkylating anticancer agents
    • (in Chinese)
    • Zhuang YY, Zhou CH, Wang YF, Li DH. Advances in the research of the alkylating anticancer agents. Chin Pharma J 2008; 44: 1281-7 (in Chinese).
    • (2008) Chin Pharma J , vol.44 , pp. 1281-1287
    • Zhuang, Y.Y.1    Zhou, C.H.2    Wang, Y.F.3    Li, D.H.4
  • 56
    • 78650719442 scopus 로고    scopus 로고
    • Design, synthesis, and biological evaluation of novel water-soluble N-mustards as potential anticancer agents
    • Kapuriya N, Kakadiya R, Dong HJ, et al. Design, synthesis, and biological evaluation of novel water-soluble N-mustards as potential anticancer agents. Bioorg Med Chem 2011; 19: 471-85.
    • (2011) Bioorg Med Chem , vol.19 , pp. 471-485
    • Kapuriya, N.1    Kakadiya, R.2    Dong, H.J.3
  • 60
    • 77956565182 scopus 로고    scopus 로고
    • Synthesis of porphyrin-nitroimidazole derivatives and their radiosensitization
    • (in Chinese)
    • Yu KG, Liu JC, Zhou CH, Diao JL, Xu T, Li DH. Synthesis of porphyrin-nitroimidazole derivatives and their radiosensitization. Chin J Med Chem 2008; 18: 414-9 (in Chinese).
    • (2008) Chin J Med Chem , vol.18 , pp. 414-419
    • Yu, K.G.1    Liu, J.C.2    Zhou, C.H.3    Diao, J.L.4    Xu, T.5    Li, D.H.6
  • 61
    • 77954895070 scopus 로고    scopus 로고
    • Progress in anti-tumor agents: Triazoles
    • (in Chinese)
    • Mi JL, Wu J, Zhou CH. Progress in anti-tumor agents: triazoles. West China J Pharm Sci 2008; 23: 84-6 (in Chinese).
    • (2008) West China J Pharm Sci , vol.23 , pp. 84-86
    • Mi, J.L.1    Wu, J.2    Zhou, C.H.3
  • 62
    • 80455129142 scopus 로고    scopus 로고
    • Recent advances in the researches of triazole compounds as medicinal drugs
    • (in Chinese)
    • Wang Y, Zhou CH. Recent advances in the researches of triazole compounds as medicinal drugs. Scientia Sinica Chemica 2011; 41: 1429-56 (in Chinese).
    • (2011) Scientia Sinica Chemica , vol.41 , pp. 1429-1456
    • Wang, Y.1    Zhou, C.H.2
  • 63
    • 65349138906 scopus 로고    scopus 로고
    • Advances in the research of benzimidazole drugs
    • (in Chinese)
    • Meng JP, Geng RX, Zhou CH, Gan LL. Advances in the research of benzimidazole drugs. Chin J New Drugs 2009; 18: 1505-14 (in Chinese).
    • (2009) Chin J New Drugs , vol.18 , pp. 1505-1514
    • Meng, J.P.1    Geng, R.X.2    Zhou, C.H.3    Gan, L.L.4
  • 64
    • 77952917993 scopus 로고    scopus 로고
    • Assessing women at high risk of breast cancer: A review of risk assessment models
    • Amir E, Freedman OC, Seruga B, Evans DG. Assessing women at high risk of breast cancer: a review of risk assessment models. J Natl Cancer Inst 2010; 102: 680-91.
    • (2010) J Natl Cancer Inst , vol.102 , pp. 680-691
    • Amir, E.1    Freedman, O.C.2    Seruga, B.3    Evans, D.G.4
  • 65
    • 80052072002 scopus 로고    scopus 로고
    • Differential effects of esculetin and daphnetin on in vitro cell proliferation and in vivo estrogenicity
    • Jiménez-Orozco FA, Rosales AAR, Vega-López A, et al. Differential effects of esculetin and daphnetin on in vitro cell proliferation and in vivo estrogenicity. Eur J Pharmacol 2011; 668: 35-41.
    • (2011) Eur J Pharmacol , vol.668 , pp. 35-41
    • Jiménez-Orozco, F.A.1    Rosales, A.A.R.2    Vega-López, A.3
  • 66
    • 78650689862 scopus 로고    scopus 로고
    • Inhibitors of NQO1: Identification of compounds more potent than dicoumarol without associated off-target effects
    • Scott KA, Barnes J, Whitehead RC, Stratford IJ, Nolan KA. Inhibitors of NQO1: identification of compounds more potent than dicoumarol without associated off-target effects. Biochem Pharmacol 2011; 81: 355-63.
    • (2011) Biochem Pharmacol , vol.81 , pp. 355-363
    • Scott, K.A.1    Barnes, J.2    Whitehead, R.C.3    Stratford, I.J.4    Nolan, K.A.5
  • 68
    • 78650204359 scopus 로고    scopus 로고
    • Mammea E/BB, an isoprenylated dihydroxycoumarin protonophore that potently uncouples mitochondrial electron transport, disrupts hypoxic signaling in tumor cells
    • Du L, Mahdi F, Jekabsons MB, Nagle DG, Zhou YD. Mammea E/BB, an isoprenylated dihydroxycoumarin protonophore that potently uncouples mitochondrial electron transport, disrupts hypoxic signaling in tumor cells. J Nat Prod 2010; 73: 1868-72.
    • (2010) J Nat Prod , vol.73 , pp. 1868-1872
    • Du, L.1    Mahdi, F.2    Jekabsons, M.B.3    Nagle, D.G.4    Zhou, Y.D.5
  • 69
    • 57849109385 scopus 로고    scopus 로고
    • Antiproliferative and apoptotic activities of tosylcyclonovobiocic acids as potent heat shock protein 90 inhibitors in human cancer cells
    • Radanyi C, Le Bras G, Marsaud V, et al. Antiproliferative and apoptotic activities of tosylcyclonovobiocic acids as potent heat shock protein 90 inhibitors in human cancer cells. Cancer Lett 2009; 274: 88-94.
    • (2009) Cancer Lett , vol.274 , pp. 88-94
    • Radanyi, C.1    Le Bras, G.2    Marsaud, V.3
  • 70
    • 41349108858 scopus 로고    scopus 로고
    • Synthesis and biological activity of simplified denoviose-coumarins related to novobiocin as potent inhibitors of heat-shock protein 90 (hsp90)
    • Radanyi C, Le Bras G, Messaoudi S, et al. Synthesis and biological activity of simplified denoviose-coumarins related to novobiocin as potent inhibitors of heat-shock protein 90 (hsp90). Bioorg Med Chem Lett 2008; 18: 2495-8.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 2495-2498
    • Radanyi, C.1    Le Bras, G.2    Messaoudi, S.3
  • 71
    • 84859771665 scopus 로고    scopus 로고
    • 3-Arylcoumarin derivatives manifest anti-proliferative activity through Hsp90 inhibition
    • Zhao HP, Yan B, Peterson LB, Blagg BSJ. 3-Arylcoumarin derivatives manifest anti-proliferative activity through Hsp90 inhibition. ACS Med Chem Lett 2012; 3: 327-31.
    • (2012) ACS Med Chem Lett , vol.3 , pp. 327-331
    • Zhao, H.P.1    Yan, B.2    Peterson, L.B.3    Blagg, B.S.J.4
  • 72
    • 84055176334 scopus 로고    scopus 로고
    • Glycosyl coumarin carbonic anhydrase IX and XII inhibitors strongly attenuate the growth of primary breast tumors
    • Touisni N, Maresca A, McDonald PC, et al. Glycosyl coumarin carbonic anhydrase IX and XII inhibitors strongly attenuate the growth of primary breast tumors. J Med Chem 2011; 54: 8271-7.
    • (2011) J Med Chem , vol.54 , pp. 8271-8277
    • Touisni, N.1    Maresca, A.2    McDonald, P.C.3
  • 73
    • 78649857406 scopus 로고    scopus 로고
    • Carbonic anhydrase inhibition/activation: Trip of a scientist around the world in the search of novel chemotypes and drug targets
    • Supuran CT. Carbonic anhydrase inhibition/activation: trip of a scientist around the world in the search of novel chemotypes and drug targets. Curr Pharm Des 2010; 16: 3233-45.
    • (2010) Curr Pharm Des , vol.16 , pp. 3233-3245
    • Supuran, C.T.1
  • 74
    • 84857757426 scopus 로고    scopus 로고
    • Inhibition of V-ATPase and carbonic anhydrases as interference strategy with tumor acidification processes
    • Perez-Sayans M, Garcia-Garcia A, Scozzafava A, Supuran CT. Inhibition of V-ATPase and carbonic anhydrases as interference strategy with tumor acidification processes. Curr Pharm Des 2012; 18: 1407-13.
    • (2012) Curr Pharm Des , vol.18 , pp. 1407-1413
    • Perez-Sayans, M.1    Garcia-Garcia, A.2    Scozzafava, A.3    Supuran, C.T.4
  • 75
    • 79955490807 scopus 로고    scopus 로고
    • Targeting tumor hypoxia: Suppression of breast tumor growth and metastasis by novel carbonic anhydrase IX inhibitors
    • Lou YM, McDonald PC, Oloumi A, et al. Targeting tumor hypoxia: suppression of breast tumor growth and metastasis by novel carbonic anhydrase IX inhibitors. Cancer Res 2011; 71: 3364-76.
    • (2011) Cancer Res , vol.71 , pp. 3364-3376
    • Lou, Y.M.1    McDonald, P.C.2    Oloumi, A.3
  • 76
    • 77953264467 scopus 로고    scopus 로고
    • Endogenous myoglobin in human breast cancer is a hallmark of luminal cancer phenotype
    • Kristiansen G, Rose M, Geisler C, et al. Endogenous myoglobin in human breast cancer is a hallmark of luminal cancer phenotype. British J Cancer 2010; 102: 1736-45.
    • (2010) British J Cancer , vol.102 , pp. 1736-1745
    • Kristiansen, G.1    Rose, M.2    Geisler, C.3
  • 77
    • 79952810375 scopus 로고    scopus 로고
    • Design, synthesis, and biological evaluation of imidazolyl derivatives of 4,7-disubstituted coumarins as aromatase inhibitors selective over 17-rhydroxylase/ C17-20 lyase
    • Stefanachi A, Favia AD, Nicolotti O, et al. Design, synthesis, and biological evaluation of imidazolyl derivatives of 4,7-disubstituted coumarins as aromatase inhibitors selective over 17-rhydroxylase/ C17-20 lyase. J Med Chem 2011; 54: 1613-25.
    • (2011) J Med Chem , vol.54 , pp. 1613-1625
    • Stefanachi, A.1    Favia, A.D.2    Nicolotti, O.3
  • 79
    • 84865760149 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of novel benzimidazole derivatives and their binding behavior with bovine serum albumin
    • Zhang SL, Damu GLV, Zhang L, Geng RX, Zhou CH. Synthesis and biological evaluation of novel benzimidazole derivatives and their binding behavior with bovine serum albumin. Eur J Med Chem 2012; 55: 164-75.
    • (2012) Eur J Med Chem , vol.55 , pp. 164-175
    • Zhang, S.L.1    Damu, G.L.V.2    Zhang, L.3    Geng, R.X.4    Zhou, C.H.5
  • 80
    • 84865360549 scopus 로고    scopus 로고
    • Synthesis and characterization of thiophene-derived amido bis-nitrogen mustard and its antimicrobial and anticancer activities
    • Tang YD, Zhang JQ, Zhang SL, Geng RX, Zhou CH. Synthesis and characterization of thiophene-derived amido bis-nitrogen mustard and its antimicrobial and anticancer activities. Chin J Chem 2012; 30: 1831-40.
    • (2012) Chin J Chem , vol.30 , pp. 1831-1840
    • Tang, Y.D.1    Zhang, J.Q.2    Zhang, S.L.3    Geng, R.X.4    Zhou, C.H.5
  • 81
    • 79251527910 scopus 로고    scopus 로고
    • Novel synthesis and antitumor evaluation of polyfunctionally substituted heterocyclic compounds derived from 2-cyano-N-(3-cyano-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)-acetamide
    • Shams HZ, Mohareb RM, Helal MH, Mahmoud AE. Novel synthesis and antitumor evaluation of polyfunctionally substituted heterocyclic compounds derived from 2-cyano-N-(3-cyano-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)-acetamide. Molecules 2011; 16: 52-73.
    • (2011) Molecules , vol.16 , pp. 52-73
    • Shams, H.Z.1    Mohareb, R.M.2    Helal, M.H.3    Mahmoud, A.E.4
  • 82
    • 66849124975 scopus 로고    scopus 로고
    • Osthole: A promising lead compound for drug discovery from a Traditional Chinese Medicine (TCM)
    • You LS, Feng S, An R, Wang XH. Osthole: a promising lead compound for drug discovery from a Traditional Chinese Medicine (TCM). Nat Prod Commun 2009; 4: 297-302.
    • (2009) Nat Prod Commun , vol.4 , pp. 297-302
    • You, L.S.1    Feng, S.2    An, R.3    Wang, X.H.4
  • 83
    • 37549069399 scopus 로고    scopus 로고
    • Enhancement of bone morphogenetic protein-2 expression and bone formation by coumarin derivatives via p38 and ERK-dependent pathway in osteoblasts
    • Tang CH, Yang RS, Chien MY, Chen CC, Fu WM. Enhancement of bone morphogenetic protein-2 expression and bone formation by coumarin derivatives via p38 and ERK-dependent pathway in osteoblasts. Eur J Pharmacol 2008; 579: 40-9.
    • (2008) Eur J Pharmacol , vol.579 , pp. 40-49
    • Tang, C.H.1    Yang, R.S.2    Chien, M.Y.3    Chen, C.C.4    Fu, W.M.5
  • 84
    • 78449298875 scopus 로고    scopus 로고
    • Discovery of novel osthole derivatives as potential anti-breast cancer treatment
    • You LS, An R, Wang XH, Li YM. Discovery of novel osthole derivatives as potential anti-breast cancer treatment. Bioorg Med Chem Lett 2010; 20: 7426-8.
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 7426-7428
    • You, L.S.1    An, R.2    Wang, X.H.3    Li, Y.M.4
  • 85
    • 77958103409 scopus 로고    scopus 로고
    • Synthesis and evaluation of noviose replacements on novobiocin that manifest antiproliferative activity
    • Zhao HP, Kusuma BR, Blaǧǧ BSJ. Synthesis and evaluation of noviose replacements on novobiocin that manifest antiproliferative activity. ACS Med Chem Lett 2010; 1: 311-5.
    • (2010) ACS Med Chem Lett , vol.1 , pp. 311-315
    • Zhao, H.P.1    Kusuma, B.R.2    Blaǧǧ, B.S.J.3
  • 86
    • 79958171071 scopus 로고    scopus 로고
    • Engineering an antibiotic to fight cancer: Optimization of the novobiocin scaffold to produce anti-proliferative agents
    • Zhao HP, Donnelly AC, Kusuma BR, et al. Engineering an antibiotic to fight cancer: optimization of the novobiocin scaffold to produce anti-proliferative agents. J Med Chem 2011; 54: 3839-53.
    • (2011) J Med Chem , vol.54 , pp. 3839-3853
    • Zhao, H.P.1    Donnelly, A.C.2    Kusuma, B.R.3
  • 87
    • 66749178359 scopus 로고    scopus 로고
    • Antitumor agents. 266. Design, synthesis, and biological evaluation of novel 2-(furan-2-yl)naphthalen-1-ol derivatives as potent and selective antibreast cancer agents
    • Dong YZ, Shi Q, Liu YN, Wang X, Bastow KF, Lee KH. Antitumor agents. 266. Design, synthesis, and biological evaluation of novel 2-(furan-2-yl)naphthalen-1-ol derivatives as potent and selective antibreast cancer agents. J Med Chem 2009; 52: 3586-90.
    • (2009) J Med Chem , vol.52 , pp. 3586-3590
    • Dong, Y.Z.1    Shi, Q.2    Liu, Y.N.3    Wang, X.4    Bastow, K.F.5    Lee, K.H.6
  • 88
    • 78149281220 scopus 로고    scopus 로고
    • Neo-tanshinlactone inspired synthesis, in vitro evaluation of novel substituted benzocoumarin derivatives as potent anti-breast cancer agents
    • Sashidhara KV, Rosaiah JN, Kumar M, et al. Neo-tanshinlactone inspired synthesis, in vitro evaluation of novel substituted benzocoumarin derivatives as potent anti-breast cancer agents. Bioorg Med Chem Lett 2010; 20: 7127-31.
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 7127-7131
    • Sashidhara, K.V.1    Rosaiah, J.N.2    Kumar, M.3
  • 89
    • 67651092267 scopus 로고    scopus 로고
    • Synthesis and evaluation of novel substituted 5-hydroxycoumarin and pyranocoumarin derivatives exhibiting significant antiproliferative activity against breast cancer cell lines
    • Mao WW, Wang TT, Zeng HP, Wang ZY, Chen JP, Shen JG. Synthesis and evaluation of novel substituted 5-hydroxycoumarin and pyranocoumarin derivatives exhibiting significant antiproliferative activity against breast cancer cell lines. Bioorg Med Chem Lett 2009; 19: 4570-3.
    • (2009) Bioorg Med Chem Lett , vol.19 , pp. 4570-4573
    • Mao, W.W.1    Wang, T.T.2    Zeng, H.P.3    Wang, Z.Y.4    Chen, J.P.5    Shen, J.G.6
  • 90
    • 39449103420 scopus 로고    scopus 로고
    • Induction of apoptosis in human leukaemia HL-60 cells by furanone-coumarins from Murraya siamensis
    • Murata T, Itoigawa M, Ito C, et al. Induction of apoptosis in human leukaemia HL-60 cells by furanone-coumarins from Murraya siamensis. J Pharm Pharmacol 2008; 60: 385-9.
    • (2008) J Pharm Pharmacol , vol.60 , pp. 385-389
    • Murata, T.1    Itoigawa, M.2    Ito, C.3
  • 91
    • 67650095567 scopus 로고    scopus 로고
    • Synthesis and multidrug resistance reversal activity of dihydroptychantol A and its novel derivatives
    • Sun B, Yuan HQ, Xi GM, Ma YD, Lou HX. Synthesis and multidrug resistance reversal activity of dihydroptychantol A and its novel derivatives. Bioorg Med Chem 2009; 17: 4981-9.
    • (2009) Bioorg Med Chem , vol.17 , pp. 4981-4989
    • Sun, B.1    Yuan, H.Q.2    Xi, G.M.3    Ma, Y.D.4    Lou, H.X.5
  • 92
    • 79957484072 scopus 로고    scopus 로고
    • Coumarins from Cicuta virosa and their modulating effects onmultidrug-resistant (MDR) tumors
    • Wang SQ, Li X, Wang XN, Wei NN, Lou HX. Coumarins from Cicuta virosa and their modulating effects onmultidrug-resistant (MDR) tumors. Phytochem Lett 2011; 4: 97-100.
    • (2011) Phytochem Lett , vol.4 , pp. 97-100
    • Wang, S.Q.1    Li, X.2    Wang, X.N.3    Wei, N.N.4    Lou, H.X.5
  • 93
    • 78650204852 scopus 로고    scopus 로고
    • Sesquiterpene coumarins from Ferula gumosa
    • Iranshahi M, Masullo M, Asili A, et al. Sesquiterpene coumarins from Ferula gumosa. J Nat Prod 2010; 73: 1958-62.
    • (2010) J Nat Prod , vol.73 , pp. 1958-1962
    • Iranshahi, M.1    Masullo, M.2    Asili, A.3
  • 94
    • 75749123095 scopus 로고    scopus 로고
    • Tumor-selective cytotoxicity of benzo[c]phenanthridine derivatives from Toddalia asiatica Lam
    • Iwasaki H, Okabe T, Takara K, Toda T, Shimatani M, Oku H. Tumor-selective cytotoxicity of benzo[c]phenanthridine derivatives from Toddalia asiatica Lam. Cancer Chemother Pharmacol 2010; 65: 719-26.
    • (2010) Cancer Chemother Pharmacol , vol.65 , pp. 719-726
    • Iwasaki, H.1    Okabe, T.2    Takara, K.3    Toda, T.4    Shimatani, M.5    Oku, H.6
  • 95
    • 84861821328 scopus 로고    scopus 로고
    • Toddaculin, a natural coumarin from Toddalia asiatica, induces differentiation and apoptosis in U-937 leukemic cells
    • Vázquez R, Riveiro ME, Vermeulen M, et al. Toddaculin, a natural coumarin from Toddalia asiatica, induces differentiation and apoptosis in U-937 leukemic cells. Phytomedicine 2012; 19: 737-46.
    • (2012) Phytomedicine , vol.19 , pp. 737-746
    • Vázquez, R.1    Riveiro, M.E.2    Vermeulen, M.3
  • 96
    • 38949125112 scopus 로고    scopus 로고
    • Hybrid molecules with a dual mode of action: Dream or reality?
    • Meunier B. Hybrid molecules with a dual mode of action: dream or reality? Acc Chem Res 2008; 41: 69-77.
    • (2008) Acc Chem Res , vol.41 , pp. 69-77
    • Meunier, B.1
  • 97
    • 80054775965 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of hydroxylated 3-phenylcoumarins as antioxidants and antiproliferative agents
    • Yang J, Liu GY, Dai F, et al. Synthesis and biological evaluation of hydroxylated 3-phenylcoumarins as antioxidants and antiproliferative agents. Bioorg Med Chem Lett 2011; 21: 6420-5.
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 6420-6425
    • Yang, J.1    Liu, G.Y.2    Dai, F.3
  • 98
    • 69249134264 scopus 로고    scopus 로고
    • Towards establishing structure-activity relationships for oxygenated coumarins as differentiation inducers of promonocytic leukemic cells
    • Riveiro ME, Maes D, Vázquez R, et al. Towards establishing structure-activity relationships for oxygenated coumarins as differentiation inducers of promonocytic leukemic cells. Bioorg Med Chem 2009; 17: 6547-59.
    • (2009) Bioorg Med Chem , vol.17 , pp. 6547-6559
    • Riveiro, M.E.1    Maes, D.2    Vázquez, R.3
  • 99
    • 77952542786 scopus 로고    scopus 로고
    • Lung cancer cell lines: Useless artifacts or invaluable tools for medical science?
    • Gazdar AF, Gao BN, Minna JD. Lung cancer cell lines: useless artifacts or invaluable tools for medical science? Lung Cancer 2010; 68: 309-18.
    • (2010) Lung Cancer , vol.68 , pp. 309-318
    • Gazdar, A.F.1    Gao, B.N.2    Minna, J.D.3
  • 100
    • 48349106315 scopus 로고    scopus 로고
    • Potential of resveratrol in anticancer and anti-inflammatory therapy
    • Udenigwe CC, Ramprasath VR, Aluko RE, Jones PJH. Potential of resveratrol in anticancer and anti-inflammatory therapy. Nutr Rev 2008; 66: 445-54.
    • (2008) Nutr Rev , vol.66 , pp. 445-454
    • Udenigwe, C.C.1    Ramprasath, V.R.2    Aluko, R.E.3    Jones, P.J.H.4
  • 101
    • 77953134777 scopus 로고    scopus 로고
    • Design, synthesis and anticancer activities of stilbene-coumarin hybrid compounds: Identification of novel proapoptotic agents
    • Belluti F, Fontana G, Bo LD, Carenini N, Giommarelli C, Zunino F. Design, synthesis and anticancer activities of stilbene-coumarin hybrid compounds: identification of novel proapoptotic agents. Bioorg Med Chem 2010; 18: 3543-50.
    • (2010) Bioorg Med Chem , vol.18 , pp. 3543-3550
    • Belluti, F.1    Fontana, G.2    Bo, L.D.3    Carenini, N.4    Giommarelli, C.5    Zunino, F.6
  • 103
    • 54049104981 scopus 로고    scopus 로고
    • Synthesis and structure-activity relationships of novel 1-arylmethyl-3-aryl-1H-pyrazole-5-carbohydrazide hydrazone derivatives as potential agents A549 lung cancer cells
    • Xia Y, Fan CD, Zhao BX, Zhao J, Shin DS, Miao JY. Synthesis and structure-activity relationships of novel 1-arylmethyl-3-aryl-1H-pyrazole-5-carbohydrazide hydrazone derivatives as potential agents A549 lung cancer cells. Eur J Med Chem 2008; 43: 2347-53.
    • (2008) Eur J Med Chem , vol.43 , pp. 2347-2353
    • Xia, Y.1    Fan, C.D.2    Zhao, B.X.3    Zhao, J.4    Shin, D.S.5    Miao, J.Y.6
  • 104
    • 72049108891 scopus 로고    scopus 로고
    • Microwave assisted synthesis and antimicrobial activity of 2-quinoxalinone-3-hydrazone derivatives
    • Ajani OO, Obafemi CA, Nwinyi OC, Akinpelu DA. Microwave assisted synthesis and antimicrobial activity of 2-quinoxalinone-3-hydrazone derivatives. Bioorg Med Chem 2010; 18: 214-21.
    • (2010) Bioorg Med Chem , vol.18 , pp. 214-221
    • Ajani, O.O.1    Obafemi, C.A.2    Nwinyi, O.C.3    Akinpelu, D.A.4
  • 105
    • 61349184617 scopus 로고    scopus 로고
    • Synthesis of novel substituted pyrazole-5-carbohydrazide hydrazone derivatives and discovery of a potent apoptosis inducer in A549 lung cancer cells
    • Zheng LW, Wu LL, Zhao BX, Dong WL, Miao YJ. Synthesis of novel substituted pyrazole-5-carbohydrazide hydrazone derivatives and discovery of a potent apoptosis inducer in A549 lung cancer cells. Bioorg Med Chem 2009; 17: 1957-62.
    • (2009) Bioorg Med Chem , vol.17 , pp. 1957-1962
    • Zheng, L.W.1    Wu, L.L.2    Zhao, B.X.3    Dong, W.L.4    Miao, Y.J.5
  • 106
    • 79251515011 scopus 로고    scopus 로고
    • Novel synthesis of hydrazidehydrazone derivatives and their utilization in the synthesis of cou marin, pyridine, thiazole and thiophene derivatives with antitumor activity
    • Mohareb RM, Fleita DH, Sakka OK. Novel synthesis of hydrazidehydrazone derivatives and their utilization in the synthesis of cou marin, pyridine, thiazole and thiophene derivatives with antitumor activity. Molecules 2011; 16: 16-27.
    • (2011) Molecules , vol.16 , pp. 16-27
    • Mohareb, R.M.1    Fleita, D.H.2    Sakka, O.K.3
  • 107
    • 84862782938 scopus 로고    scopus 로고
    • Antitumor agents 292. Design, synthesis and pharmacological study of S-and O-substituted 7-mercapto-or hydroxy-coumarins and chromones as potent cytotoxic agents
    • Chen Y, Liu HR, Liu HS, et al. Antitumor agents 292. Design, synthesis and pharmacological study of S-and O-substituted 7-mercapto-or hydroxy-coumarins and chromones as potent cytotoxic agents. Eur J Med Chem 2012; 49: 74-85.
    • (2012) Eur J Med Chem , vol.49 , pp. 74-85
    • Chen, Y.1    Liu, H.R.2    Liu, H.S.3
  • 108
    • 68349090374 scopus 로고    scopus 로고
    • Antioxidant and anticancer activities of 8-hydroxypsoralen isolated from wampee [Clausena lansium (Lour.) Skeels] peel
    • Prasad KN, Xie HH, Hao J, et al. Antioxidant and anticancer activities of 8-hydroxypsoralen isolated from wampee [Clausena lansium (Lour.) Skeels] peel. Food Chem 2010; 118: 62-6.
    • (2010) Food Chem , vol.118 , pp. 62-66
    • Prasad, K.N.1    Xie, H.H.2    Hao, J.3
  • 109
    • 84857579184 scopus 로고    scopus 로고
    • New progress in study on biological activities of chalcones
    • (in Chinese)
    • Jin L, Yan CY, Gan LL, Zhou CH. New progress in study on biological activities of chalcones. Chin J Biochem Pharm 2010; 31: 358-61 (in Chinese).
    • (2010) Chin J Biochem Pharm , vol.31 , pp. 358-361
    • Jin, L.1    Yan, C.Y.2    Gan, L.L.3    Zhou, C.H.4
  • 110
    • 48449096245 scopus 로고    scopus 로고
    • Synthesis and cytotoxic, anti-inflammatory, and anti-oxidant activities of 2',5'-dialkoxylchalcones as cancer chemopreventive agents
    • Cheng JH, Hung CF, Yang SC, Wang JP, Won SJ, Lin CN. Synthesis and cytotoxic, anti-inflammatory, and anti-oxidant activities of 2',5'-dialkoxylchalcones as cancer chemopreventive agents. Bioorg Med Chem 2008; 16: 7270-6.
    • (2008) Bioorg Med Chem , vol.16 , pp. 7270-7276
    • Cheng, J.H.1    Hung, C.F.2    Yang, S.C.3    Wang, J.P.4    Won, S.J.5    Lin, C.N.6
  • 111
    • 78449284852 scopus 로고    scopus 로고
    • Synthesis and in vitro evaluation of novel coumarin-chalcone hybrids as potential anticancer agents
    • Sashidhara KV, Kumar A, Kumar M, Sarkar J, Sinha S. Synthesis and in vitro evaluation of novel coumarin-chalcone hybrids as potential anticancer agents. Bioorg Med Chem Lett 2010; 20: 7205-11.
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 7205-7211
    • Sashidhara, K.V.1    Kumar, A.2    Kumar, M.3    Sarkar, J.4    Sinha, S.5
  • 113
    • 57649165278 scopus 로고    scopus 로고
    • Identification and physiological evaluation of the components from Citrus fruits as potential drugs for anti-corpulence and anticancer
    • Hirata T, Fujii M, Akita K, et al. Identification and physiological evaluation of the components from Citrus fruits as potential drugs for anti-corpulence and anticancer. Bioorg Med Chem 2009; 17: 25-8.
    • (2009) Bioorg Med Chem , vol.17 , pp. 25-28
    • Hirata, T.1    Fujii, M.2    Akita, K.3
  • 114
    • 41849084518 scopus 로고    scopus 로고
    • Development of novobiocin analogs that manifest antiproliferative activity against several cancer cell lines
    • Burlison JA, Avila C, Vielhauer G, Lubbers DJ, Holzbeierlein J, Blagg BSJ. Development of novobiocin analogs that manifest antiproliferative activity against several cancer cell lines. J Org Chem 2008; 73: 2130-7.
    • (2008) J Org Chem , vol.73 , pp. 2130-2137
    • Burlison, J.A.1    Avila, C.2    Vielhauer, G.3    Lubbers, D.J.4    Holzbeierlein, J.5    Blagg, B.S.J.6
  • 115
    • 44849135016 scopus 로고    scopus 로고
    • Bioactive food components and cancer risk reduction
    • Stan SD, Kar S, Stoner GD, Singh SV. Bioactive food components and cancer risk reduction. J Cell Biochem 2008; 104: 339-56.
    • (2008) J Cell Biochem , vol.104 , pp. 339-356
    • Stan, S.D.1    Kar, S.2    Stoner, G.D.3    Singh, S.V.4
  • 116
    • 84857033328 scopus 로고    scopus 로고
    • Coumarin polysulfides inhibit cell growth and induce apoptosis in HCT116 colon cancer cells
    • Saidu NEB, Valente S, Bana E, Kirsch G, Bagrel D, Montenarh M. Coumarin polysulfides inhibit cell growth and induce apoptosis in HCT116 colon cancer cells. Bioorg Med Chem 2012; 20: 1584-93.
    • (2012) Bioorg Med Chem , vol.20 , pp. 1584-1593
    • Saidu, N.E.B.1    Valente, S.2    Bana, E.3    Kirsch, G.4    Bagrel, D.5    Montenarh, M.6
  • 117
    • 51349169728 scopus 로고    scopus 로고
    • Novel anticancer agents, kayeassamins C-I from the power of Kayea assamica of Myanmar
    • Win NN, Awale S, Esumi H, Tezuka Y, Kadota S. Novel anticancer agents, kayeassamins C-I from the power of Kayea assamica of Myanmar. Bioorg Med Chem 2008; 16: 8653-60.
    • (2008) Bioorg Med Chem , vol.16 , pp. 8653-8660
    • Win, N.N.1    Awale, S.2    Esumi, H.3    Tezuka, Y.4    Kadota, S.5
  • 119
    • 70949090659 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of coumarin-based inhibitors of NAD(P)H: Quinone qxidoreductase-1 (NQO1)
    • Nolan KA, Doncaster JR, Dunstan MS, et al. Synthesis and biological evaluation of coumarin-based inhibitors of NAD(P)H: quinone qxidoreductase-1 (NQO1). J Med Chem 2009; 52: 7142-56.
    • (2009) J Med Chem , vol.52 , pp. 7142-7156
    • Nolan, K.A.1    Doncaster, J.R.2    Dunstan, M.S.3
  • 120
    • 74649083308 scopus 로고    scopus 로고
    • Constituents of Corydalis heterocarpa and their anti-proliferative effects on human cancer cells
    • Kim YA, Kong CS, Yea SS, Seo Y. Constituents of Corydalis heterocarpa and their anti-proliferative effects on human cancer cells. Food Chem Toxicol 2010; 48: 722-8.
    • (2010) Food Chem Toxicol , vol.48 , pp. 722-728
    • Kim, Y.A.1    Kong, C.S.2    Yea, S.S.3    Seo, Y.4
  • 121
    • 53349161932 scopus 로고    scopus 로고
    • Structure of the tribolium castaneum telomerase catalytic subunit TERT
    • Gillis AJ, Schuller AP, Skordalakes E. Structure of the tribolium castaneum telomerase catalytic subunit TERT. Nature 2008; 455: 633-7.
    • (2008) Nature , vol.455 , pp. 633-637
    • Gillis, A.J.1    Schuller, A.P.2    Skordalakes, E.3
  • 122
    • 77957657932 scopus 로고    scopus 로고
    • Synthesis and molecular docking study of novel coumarin derivatives containing 4,5-dihydropyrazole moiety as potential antitumor agents
    • Liu XH, Liu HF, Chen J, et al. Synthesis and molecular docking study of novel coumarin derivatives containing 4,5-dihydropyrazole moiety as potential antitumor agents. Bioorg Med Chem Lett 2010; 20: 5705-8.
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 5705-5708
    • Liu, X.H.1    Liu, H.F.2    Chen, J.3
  • 123
    • 84862793621 scopus 로고    scopus 로고
    • Anti-mitotic potential of 7-diethylamino-3(2'-benzoxazolyl)-coumarin in 5-fluorouracilresistant human gastric cancer cell line SNU620/5-FU
    • Kim NH, Kim SN, Oh JS, Lee S, Kim YK. Anti-mitotic potential of 7-diethylamino-3(2'-benzoxazolyl)-coumarin in 5-fluorouracilresistant human gastric cancer cell line SNU620/5-FU. Biochem Biophys Res Commun 2012; 418: 616-21.
    • (2012) Biochem Biophys Res Commun , vol.418 , pp. 616-621
    • Kim, N.H.1    Kim, S.N.2    Oh, J.S.3    Lee, S.4    Kim, Y.K.5
  • 124
    • 56449125983 scopus 로고    scopus 로고
    • The design, synthesis, and evaluation of coumarin ring derivatives of the novobiocin scaffold that exhibit antiproliferative activity
    • Donnelly AC, Mays JR, Burlison JA, et al. The design, synthesis, and evaluation of coumarin ring derivatives of the novobiocin scaffold that exhibit antiproliferative activity. J Org Chem 2008; 73: 8901-20.
    • (2008) J Org Chem , vol.73 , pp. 8901-8920
    • Donnelly, A.C.1    Mays, J.R.2    Burlison, J.A.3
  • 125
    • 84876476017 scopus 로고    scopus 로고
    • Cytotoxicity evaluation of coumarin derivatives containing 4-bromophenyl or anthracene moieties
    • doi: 10.1007/s11164-012-0716-5
    • Zhang H, Zhao M, Yu TZ, Zhao YL, Fan DW, Zhang SD. Cytotoxicity evaluation of coumarin derivatives containing 4-bromophenyl or anthracene moieties. Res Chem Intermed 2012; doi: 10.1007/s11164-012-0716-5.
    • (2012) Res Chem Intermed
    • Zhang, H.1    Zhao, M.2    Yu, T.Z.3    Zhao, Y.L.4    Fan, D.W.5    Zhang, S.D.6
  • 126
    • 56949090985 scopus 로고    scopus 로고
    • 6-Substituted 2-oxo-2H-1-benzopyran-3-carboxylic acid derivatives in a new approach of the treatment of cancer cell invasion and metastasis
    • Kempen I, Hemmer M, Counerotte S, et al. 6-Substituted 2-oxo-2H-1-benzopyran-3-carboxylic acid derivatives in a new approach of the treatment of cancer cell invasion and metastasis. Eur J Med Chem 2008; 43: 2735-50.
    • (2008) Eur J Med Chem , vol.43 , pp. 2735-2750
    • Kempen, I.1    Hemmer, M.2    Counerotte, S.3
  • 127
    • 78650889379 scopus 로고    scopus 로고
    • Antiproliferative and proapoptotic activity of GUT-70 mediated through potent inhibition of Hsp90 in mantle cell lymphoma
    • Jin L, Tabe Y, Kimura S, et al. Antiproliferative and proapoptotic activity of GUT-70 mediated through potent inhibition of Hsp90 in mantle cell lymphoma. British J Cancer 2011; 104: 91-100.
    • (2011) British J Cancer , vol.104 , pp. 91-100
    • Jin, L.1    Tabe, Y.2    Kimura, S.3
  • 128
    • 72049089820 scopus 로고    scopus 로고
    • Coumarins as novel 17β-hydroxysteroid dehydrogenase type 3 inhibitors for potential treatment of prostate cancer
    • Harada K, Kubo H, Tomigahara Y, et al. Coumarins as novel 17β-hydroxysteroid dehydrogenase type 3 inhibitors for potential treatment of prostate cancer. Bioorg Med Chem Lett 2010; 20: 272-5.
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 272-275
    • Harada, K.1    Kubo, H.2    Tomigahara, Y.3
  • 129
    • 79151470320 scopus 로고    scopus 로고
    • A coumarin derivative (RKS262) inhibits cell-cycle progression, causes pro-apoptotic signaling and cytotoxicity in ovarian cancer cells
    • Singh RK, Lange TS, Kim KK, Brard L. A coumarin derivative (RKS262) inhibits cell-cycle progression, causes pro-apoptotic signaling and cytotoxicity in ovarian cancer cells. Invest New Drugs 2011; 29: 63-72.
    • (2011) Invest New Drugs , vol.29 , pp. 63-72
    • Singh, R.K.1    Lange, T.S.2    Kim, K.K.3    Brard, L.4
  • 130
    • 15944389028 scopus 로고    scopus 로고
    • Simple coumarins and analogs in medicinal chemistry: Occurrence, synthesis and biological activity
    • Borges F, Roleira F, Milhazes N, Santana L, Uriarte E. Simple coumarins and analogs in medicinal chemistry: occurrence, synthesis and biological activity. Curr Med Chem 2005; 12: 887-916.
    • (2005) Curr Med Chem , vol.12 , pp. 887-916
    • Borges, F.1    Roleira, F.2    Milhazes, N.3    Santana, L.4    Uriarte, E.5
  • 132
    • 38749125127 scopus 로고    scopus 로고
    • Synthesis and protective effects of coumarin derivatives against oxidative stress induced by doxorubicin
    • Beillerot A, Rodríguez Domínguez JC, Kirsch G, Bagrel D. Synthesis and protective effects of coumarin derivatives against oxidative stress induced by doxorubicin. Bioorg Med Chem Lett 2008; 18: 1102-5.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 1102-1105
    • Beillerot, A.1    Rodríguez, D.J.C.2    Kirsch, G.3    Bagrel, D.4
  • 133
    • 75049086152 scopus 로고    scopus 로고
    • Substituted imino and amino derivatives of 4-hydroxycoumarins as novel antioxidant, antibacterial and antifungal agents: Synthesis and in vitro assessments
    • Vukovic N, Sukdolak S, Solujic S, Niciforovic N. Substituted imino and amino derivatives of 4-hydroxycoumarins as novel antioxidant, antibacterial and antifungal agents: synthesis and in vitro assessments. Food Chem 2010; 120: 1011-8.
    • (2010) Food Chem , vol.120 , pp. 1011-1018
    • Vukovic, N.1    Sukdolak, S.2    Solujic, S.3    Niciforovic, N.4
  • 134
    • 77956891985 scopus 로고    scopus 로고
    • Expedious synthesis for α, β-unsaturated coumarin derivatives using boran chelates: A novel class of potential antibacterial and antioxidant agents
    • Hamdi N, Bouabdallah F, Romerosa A, Benhassen R. Expedious synthesis for α, β-unsaturated coumarin derivatives using boran chelates: a novel class of potential antibacterial and antioxidant agents. CRChim 2010; 13: 1261-8.
    • (2010) CRChim , vol.13 , pp. 1261-1268
    • Hamdi, N.1    Bouabdallah, F.2    Romerosa, A.3    Benhassen, R.4
  • 135
    • 80052026606 scopus 로고    scopus 로고
    • A rapid access to new coumarinyl chalcone and substituted chromeno[4,3-c]pyrazol-4(1H)-ones and their antibacterial and DPPH radical scavenging activities
    • Hamdi N, Fischmeister C, Puerta MC, Valerga P. A rapid access to new coumarinyl chalcone and substituted chromeno[4,3-c]pyrazol-4(1H)-ones and their antibacterial and DPPH radical scavenging activities. Med Chem Res 2011; 20: 522-30.
    • (2011) Med Chem Res , vol.20 , pp. 522-530
    • Hamdi, N.1    Fischmeister, C.2    Puerta, M.C.3    Valerga, P.4
  • 136
    • 67349140661 scopus 로고    scopus 로고
    • Synthesis and evaluation of the antioxidant and anti-inflammatory activity of novel coumarin-3-aminoamides and their alpha-lipoic acid adducts
    • Melagraki G, Afantitis A, Igglessi-Markopoulou O, et al. Synthesis and evaluation of the antioxidant and anti-inflammatory activity of novel coumarin-3-aminoamides and their alpha-lipoic acid adducts. Eur J Med Chem 2009; 44: 3020-6.
    • (2009) Eur J Med Chem , vol.44 , pp. 3020-3026
    • Melagraki, G.1    Afantitis, A.2    Igglessi-Markopoulou, O.3
  • 137
    • 77955843923 scopus 로고    scopus 로고
    • Antioxidant properties of 4-methylcoumarins in in vitro cell-free systems
    • Morabito G, Trombetta D, Brajendra KS, et al. Antioxidant properties of 4-methylcoumarins in in vitro cell-free systems. Biochimie 2010; 92: 1101-7.
    • (2010) Biochimie , vol.92 , pp. 1101-1107
    • Morabito, G.1    Trombetta, D.2    Brajendra, K.S.3
  • 138
    • 84862024864 scopus 로고    scopus 로고
    • Antioxidant activities and cytotoxicity of selected coumarin derivatives: Preliminary results of a structureactivity relationship study using computational tools
    • Gacche RN, Jadhav SG. Antioxidant activities and cytotoxicity of selected coumarin derivatives: preliminary results of a structureactivity relationship study using computational tools. J Exp Clin Med 2012; 4: 165-9.
    • (2012) J Exp Clin Med , vol.4 , pp. 165-169
    • Gacche, R.N.1    Jadhav, S.G.2
  • 139
    • 79958856064 scopus 로고    scopus 로고
    • Antioxidant properties of 5,7-dihydroxycoumarin derivatives in in vitro cell-free and cellcontaining systems
    • Lin MH, Chou YS, Tsai YJ, Chou DS. Antioxidant properties of 5,7-dihydroxycoumarin derivatives in in vitro cell-free and cellcontaining systems. J Exp Clin Med 2011; 3: 126-31.
    • (2011) J Exp Clin Med , vol.3 , pp. 126-131
    • Lin, M.H.1    Chou, Y.S.2    Tsai, Y.J.3    Chou, D.S.4
  • 140
    • 64349120832 scopus 로고    scopus 로고
    • Novel cyano-and amidinobenzothiazole derivatives: Synthesis, antitumor evaluation, and Xray and quantitative structure-activity relationship (QSAR) analysis
    • Cáleta I, Kralj M, Marjanović M, et al. Novel cyano-and amidinobenzothiazole derivatives: synthesis, antitumor evaluation, and Xray and quantitative structure-activity relationship (QSAR) analysis. J Med Chem 2009; 52: 1744-56.
    • (2009) J Med Chem , vol.52 , pp. 1744-1756
    • Cáleta, I.1    Kralj, M.2    Marjanović, M.3
  • 141
    • 80052394421 scopus 로고    scopus 로고
    • Synthesis and free radical scavenging activity of coumarin derivatives containing a 2-methylbenzothiazoline motif
    • Khoobi M, Emami S, Dehghan G, Foroumadi A, Ramazani A, Shafiee A. Synthesis and free radical scavenging activity of coumarin derivatives containing a 2-methylbenzothiazoline motif. Arch Pharm Chem Life Sci 2011; 344: 588-94.
    • (2011) Arch Pharm Chem Life Sci , vol.344 , pp. 588-594
    • Khoobi, M.1    Emami, S.2    Dehghan, G.3    Foroumadi, A.4    Ramazani, A.5    Shafiee, A.6
  • 142
    • 80955172788 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of (2,5-dihydro-1H-pyrrol-1-yl)-2H-chromen-2-ones as free radical scavengers
    • Balabani A, Hadjipavlou-Litina DJ, Litinas KE, Mainou M, Tsironi CC, Vronteli A. Synthesis and biological evaluation of (2,5-dihydro-1H-pyrrol-1-yl)-2H-chromen-2-ones as free radical scavengers. Eur J Med Chem 2011; 46: 5894-901.
    • (2011) Eur J Med Chem , vol.46 , pp. 5894-5901
    • Balabani, A.1    Hadjipavlou-Litina, D.J.2    Litinas, K.E.3    Mainou, M.4    Tsironi, C.C.5    Vronteli, A.6
  • 143
    • 70349765548 scopus 로고    scopus 로고
    • Antioxidant and antibacterial studies of arylazopyrazoles and arylhydrazonopyrazolones containing coumarin moiety
    • Manojkumar P, Ravi TK, Gopalakrishnan S. Antioxidant and antibacterial studies of arylazopyrazoles and arylhydrazonopyrazolones containing coumarin moiety. Eur J Med Chem 2009; 44: 4690-4.
    • (2009) Eur J Med Chem , vol.44 , pp. 4690-4694
    • Manojkumar, P.1    Ravi, T.K.2    Gopalakrishnan, S.3
  • 144
    • 79958782009 scopus 로고    scopus 로고
    • Synthesis, spectroscopy and electrochemistry of new 4-(4-acetyl-5-substituted-4,5-dihydro-1,3,4-oxodiazol-2-yl)methoxy)-2H-chromen-2-ones as a novel class of potential antibacterial and antioxidant derivatives
    • Hamdi N, Passarelli V, Romerosa A. Synthesis, spectroscopy and electrochemistry of new 4-(4-acetyl-5-substituted-4,5-dihydro-1,3,4-oxodiazol-2-yl)methoxy)-2H-chromen-2-ones as a novel class of potential antibacterial and antioxidant derivatives. C R Chim 2011; 14: 548-55.
    • (2011) C R Chim , vol.14 , pp. 548-555
    • Hamdi, N.1    Passarelli, V.2    Romerosa, A.3
  • 145
    • 84861860917 scopus 로고    scopus 로고
    • Synthesis, antitumor and antioxidant evaluation of some new thiazole and thiophene derivatives incorporated coumarin moiety
    • Gouda MA, Berghot MA, Baz EA, Hamama WS. Synthesis, antitumor and antioxidant evaluation of some new thiazole and thiophene derivatives incorporated coumarin moiety. Med Chem Res 2012; 21: 1062-70.
    • (2012) Med Chem Res , vol.21 , pp. 1062-1070
    • Gouda, M.A.1    Berghot, M.A.2    Baz, E.A.3    Hamama, W.S.4
  • 147
    • 80054735839 scopus 로고    scopus 로고
    • Synthesis and antioxidant activities of novel 4-Schiff base-7-benzyloxy-coumarin derivatives
    • Zhang Y, Zou BQ, Chen ZF, et al. Synthesis and antioxidant activities of novel 4-Schiff base-7-benzyloxy-coumarin derivatives. Bioorg Med Chem Lett 2011; 21: 6811-5.
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 6811-6815
    • Zhang, Y.1    Zou, B.Q.2    Chen, Z.F.3
  • 148
    • 77954313236 scopus 로고    scopus 로고
    • A novel synthesis of 3-aryl coumarins and evaluation of their antioxidant and lipoxygenase inhibitory activity
    • Roussaki M, Kontogiorgis CA, Hadjipavlou-Litina D, Hamilakis S, Detsi A. A novel synthesis of 3-aryl coumarins and evaluation of their antioxidant and lipoxygenase inhibitory activity. Bioorg Med Chem Lett 2010; 20: 3889-92.
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 3889-3892
    • Roussaki, M.1    Kontogiorgis, C.A.2    Hadjipavlou-Litina, D.3    Hamilakis, S.4    Detsi, A.5
  • 150
    • 77950825003 scopus 로고    scopus 로고
    • Two new coumarins from the chloroform extract of Angelica urumiensis from Iran
    • Mohammadi M, Yousefi M, Habibi Z, Shafiee A. Two new coumarins from the chloroform extract of Angelica urumiensis from Iran. Chem Pharm Bull 2010; 58: 546-8.
    • (2010) Chem Pharm Bull , vol.58 , pp. 546-548
    • Mohammadi, M.1    Yousefi, M.2    Habibi, Z.3    Shafiee, A.4
  • 151
    • 80052642320 scopus 로고    scopus 로고
    • Coumarin-based bioactive compounds: Facile synthesis and biological evaluation of coumarin-fused 1,4-thiazepines
    • Khoobi M, Foroumadi A, Emami S, et al. Coumarin-based bioactive compounds: facile synthesis and biological evaluation of coumarin-fused 1,4-thiazepines. Chem Biol Drug Des 2011; 78: 580-6.
    • (2011) Chem Biol Drug Des , vol.78 , pp. 580-586
    • Khoobi, M.1    Foroumadi, A.2    Emami, S.3
  • 152
    • 79961235102 scopus 로고    scopus 로고
    • Synthesis and evaluation of some novel furocoumarin derivatives for radical scavenging profile and cytotoxic studies
    • Ranganath YS, Harinadha BV, Sandeep G, Parameshwar R. Synthesis and evaluation of some novel furocoumarin derivatives for radical scavenging profile and cytotoxic studies. J Chem Pharm Res 2011; 3: 62-8.
    • (2011) J Chem Pharm Res , vol.3 , pp. 62-68
    • Ranganath, Y.S.1    Harinadha, B.V.2    Sandeep, G.3    Parameshwar, R.4
  • 154
    • 84866916500 scopus 로고    scopus 로고
    • Recent approaches to novel antibacterials designed after LPS structure and biochemistry
    • Gabrielli L, Capitoli A, Bini D, et al. Recent approaches to novel antibacterials designed after LPS structure and biochemistry. Curr Drug Targets 2012; 13: 1458-71.
    • (2012) Curr Drug Targets , vol.13 , pp. 1458-1471
    • Gabrielli, L.1    Capitoli, A.2    Bini, D.3
  • 155
    • 84860535850 scopus 로고    scopus 로고
    • UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase (LpxC) inhibitors: A new class of antibacterial agents
    • Zhang J, Zhang L, Li X, Xu W. UDP-3-O-(R-3-hydroxymyristoyl)-N-acetylglucosamine deacetylase (LpxC) inhibitors: a new class of antibacterial agents. Curr Med Chem 2012; 19: 2038-50.
    • (2012) Curr Med Chem , vol.19 , pp. 2038-2050
    • Zhang, J.1    Zhang, L.2    Li, X.3    Xu, W.4
  • 156
    • 84856483002 scopus 로고    scopus 로고
    • Application of SBDD to the discovery of new antibacterial drugs
    • Finn J. Application of SBDD to the discovery of new antibacterial drugs. Methods Mol Biol 2012; 841: 291-319.
    • (2012) Methods Mol Biol , vol.841 , pp. 291-319
    • Finn, J.1
  • 157
    • 77649233952 scopus 로고    scopus 로고
    • Synthesis, antibacterial and antifungal activities of some carbazole derivatives
    • Zhang FF, Gan LL, Zhou CH. Synthesis, antibacterial and antifungal activities of some carbazole derivatives. Bioorg Med Chem Lett 2010; 20: 1881-4.
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 1881-1884
    • Zhang, F.F.1    Gan, L.L.2    Zhou, C.H.3
  • 159
    • 84878639508 scopus 로고    scopus 로고
    • Recent developments in azole compounds as antibacterial and antifungal agents
    • in press
    • Peng XM, Cai GX, Zhou CH. Recent developments in azole compounds as antibacterial and antifungal agents. Curr Top Med Chem 2013; in press.
    • (2013) Curr Top Med Chem
    • Peng, X.M.1    Cai, G.X.2    Zhou, C.H.3
  • 160
    • 84876695238 scopus 로고    scopus 로고
    • Plant natural products: Their pharmaceutical potential against disease and drug resistant microbial pathogens
    • Upadhyay RK. Plant natural products: their pharmaceutical potential against disease and drug resistant microbial pathogens. J Pharm Res 2011; 4: 1179-85.
    • (2011) J Pharm Res , vol.4 , pp. 1179-1185
    • Upadhyay, R.K.1
  • 162
    • 84869081820 scopus 로고    scopus 로고
    • Synthesis and biological activities of thio-triazole derivatives as novel potential antibacterial and antifungal agents
    • Wang QP, Zhang JQ, Damu GLV, Wan K, Zhang HZ, Zhou CH. Synthesis and biological activities of thio-triazole derivatives as novel potential antibacterial and antifungal agents. Sci China Ser B: Chem 2012; 55: 2134-53.
    • (2012) Sci China Ser B: Chem , vol.55 , pp. 2134-2153
    • Wang, Q.P.1    Zhang, J.Q.2    Damu, G.L.V.3    Wan, K.4    Zhang, H.Z.5    Zhou, C.H.6
  • 166
    • 80052640394 scopus 로고    scopus 로고
    • Synthesis and antimicrobial evaluation of coumarin-based benzotriazoles and their synergistic effects with chloromycin and fluconazole
    • (in Chinese)
    • Shi Y, Zhou CH, Zhou XD, Geng RX, Ji QG. Synthesis and antimicrobial evaluation of coumarin-based benzotriazoles and their synergistic effects with chloromycin and fluconazole. Acta Pharm Sinica 2011; 46: 798-810 (in Chinese).
    • (2011) Acta Pharm Sinica , vol.46 , pp. 798-810
    • Shi, Y.1    Zhou, C.H.2    Zhou, X.D.3    Geng, R.X.4    Ji, Q.G.5
  • 167
    • 84878624194 scopus 로고    scopus 로고
    • Pharmaceuticals: Natural products and natural product models
    • Singh SB. Pharmaceuticals: natural products and natural product models. Nat Prod Chem Biol 2012; 289-324.
    • (2012) Nat Prod Chem Biol , pp. 289-324
    • Singh, S.B.1
  • 168
    • 52449111750 scopus 로고    scopus 로고
    • Membrane permeability and regulation of drug 'influx and eflux' in enterobacterial pathogens
    • Davin-Régli A, Bolla JM, James CE, et al. Membrane permeability and regulation of drug 'influx and eflux' in enterobacterial pathogens. Curr Drug Targets 2008; 9: 750-9.
    • (2008) Curr Drug Targets , vol.9 , pp. 750-759
    • Davin-Régli, A.1    Bolla, J.M.2    James, C.E.3
  • 169
    • 38349170156 scopus 로고    scopus 로고
    • Treatment of health-careassociated infections caused by Gram-negative bacteria: A consensus statement
    • Chopra I, Schofield C, Everett M, et al. Treatment of health-careassociated infections caused by Gram-negative bacteria: a consensus statement. Lancet Infect Dis 2008; 8: 133-9.
    • (2008) Lancet Infect Dis , vol.8 , pp. 133-139
    • Chopra, I.1    Schofield, C.2    Everett, M.3
  • 170
    • 69549111337 scopus 로고    scopus 로고
    • Antibiotics for emerging pathogens
    • Fischbach MA, Walsh CT. Antibiotics for emerging pathogens. Science 2009; 325: 1089-93.
    • (2009) Science , vol.325 , pp. 1089-1093
    • Fischbach, M.A.1    Walsh, C.T.2
  • 171
    • 76249132960 scopus 로고    scopus 로고
    • Antimicrobial natural products: An update on future antibiotic drug candidates
    • Saleem M, Nazir M, Ali MS, et al. Antimicrobial natural products: an update on future antibiotic drug candidates. Nat Prod Rep 2010; 27: 238-54.
    • (2010) Nat Prod Rep , vol.27 , pp. 238-254
    • Saleem, M.1    Nazir, M.2    Ali, M.S.3
  • 172
    • 78751575575 scopus 로고    scopus 로고
    • Antibacterial activity of some natural products against bacteria expressing a multidrugresistant phenotype
    • Kuete V, Alibert-Franco S, Eyong KO, et al. Antibacterial activity of some natural products against bacteria expressing a multidrugresistant phenotype. Int J Antimicrob Agents 2011; 37: 156-61.
    • (2011) Int J Antimicrob Agents , vol.37 , pp. 156-161
    • Kuete, V.1    Alibert-Franco, S.2    Eyong, K.O.3
  • 173
    • 63449117521 scopus 로고    scopus 로고
    • Antioxidant activities of extracts and main components of pigeonpea [Cajanus cajan (L.) Millsp.] leaves
    • Wu N, Fu K, Fu YJ, et al. Antioxidant activities of extracts and main components of pigeonpea [Cajanus cajan (L.) Millsp.] leaves. Molecules 2009; 14: 1032-43.
    • (2009) Molecules , vol.14 , pp. 1032-1043
    • Wu, N.1    Fu, K.2    Fu, Y.J.3
  • 174
    • 77949487407 scopus 로고    scopus 로고
    • Cajanuslactone, a new coumarin with anti-bacterial activity from pigeon pea [Cajanus cajan (L.) Millsp.] leaves
    • Kong Y, Fu YJ, Zu YG, et al. Cajanuslactone, a new coumarin with anti-bacterial activity from pigeon pea [Cajanus cajan (L.) Millsp.] leaves. Food Chem 2010; 121: 1150-5.
    • (2010) Food Chem , vol.121 , pp. 1150-1155
    • Kong, Y.1    Fu, Y.J.2    Zu, Y.G.3
  • 175
    • 63449137987 scopus 로고    scopus 로고
    • Antimicrobial and antioxidant activities of coumarins from the roots of Ferulago campestris (Apiaceae)
    • Basile A, Sorbo S, Spadaro V, et al. Antimicrobial and antioxidant activities of coumarins from the roots of Ferulago campestris (Apiaceae). Molecules 2009; 14: 939-52.
    • (2009) Molecules , vol.14 , pp. 939-952
    • Basile, A.1    Sorbo, S.2    Spadaro, V.3
  • 176
    • 84866786013 scopus 로고    scopus 로고
    • Antibacterial activity of two new monoterpene coumarins from Ethulia Conyzoides
    • El-Bassuony AA. Antibacterial activity of two new monoterpene coumarins from Ethulia Conyzoides. J Pharm Res 2009; 2: 582-4.
    • (2009) J Pharm Res , vol.2 , pp. 582-584
    • El-Bassuony, A.A.1
  • 177
    • 69249134651 scopus 로고    scopus 로고
    • Evaluation of the antimicrobial activity of some medicinal plants against enteric bacterial with particular reference to multi-drug resistant Vibrio cholerae
    • Acharyya S, Patra A, Bag PK. Evaluation of the antimicrobial activity of some medicinal plants against enteric bacterial with particular reference to multi-drug resistant Vibrio cholerae. Trop J Pharm Res 2009; 8: 231-7.
    • (2009) Trop J Pharm Res , vol.8 , pp. 231-237
    • Acharyya, S.1    Patra, A.2    Bag, P.K.3
  • 179
    • 84856216145 scopus 로고    scopus 로고
    • Alkaloid and coumarins from the green fruits of Aegle marmelos
    • Chakthong S, Weaaryee P, Puangphet P, et al. Alkaloid and coumarins from the green fruits of Aegle marmelos. Phytochemistry 2012; 75: 108-13.
    • (2012) Phytochemistry , vol.75 , pp. 108-113
    • Chakthong, S.1    Weaaryee, P.2    Puangphet, P.3
  • 180
    • 84857115811 scopus 로고    scopus 로고
    • Antimicrobial activity of ulopterol isolated from Toddalia asiatica (L.) Lam.: A traditional medicinal plant
    • Karunai Raj M, Balachandran C, Duraipandiyan V, Agastian P, Ignacimuthu S. Antimicrobial activity of ulopterol isolated from Toddalia asiatica (L.) Lam.: a traditional medicinal plant. J Ethnopharmacol 2012; 140: 161-5.
    • (2012) J Ethnopharmacol , vol.140 , pp. 161-165
    • Karunai Raj, M.1    Balachandran, C.2    Duraipandiyan, V.3    Agastian, P.4    Ignacimuthu, S.5
  • 181
    • 84857114358 scopus 로고    scopus 로고
    • Chemical investigation of Toddalia asiatica Lin. and Cardiospermum halicacabum Lin
    • Muthumani P, Meera R, Devi P, et al. Chemical investigation of Toddalia asiatica Lin. and Cardiospermum halicacabum Lin. Int J Drug Form Res 2010; 1: 224-39.
    • (2010) Int J Drug Form Res , vol.1 , pp. 224-239
    • Muthumani, P.1    Meera, R.2    Devi, P.3
  • 182
    • 70449670476 scopus 로고    scopus 로고
    • New geranyloxycoumarins from Toddalia asiatica
    • Wang F, Xu Y, Liu JK. New geranyloxycoumarins from Toddalia asiatica. J Asian Nat Prod Res 2009; 11: 752-6.
    • (2009) J Asian Nat Prod Res , vol.11 , pp. 752-756
    • Wang, F.1    Xu, Y.2    Liu, J.K.3
  • 183
    • 84862829656 scopus 로고    scopus 로고
    • Isolation and identi fication of antibacterial neo-compounds from the red ants of ChangBai Mountain, Tetramorium sp
    • Song ZW, Liu P, Yin WP, Jiang YL, Ren YL. Isolation and identi fication of antibacterial neo-compounds from the red ants of ChangBai Mountain, Tetramorium sp. Bioorg Med Chem Lett 2012; 22: 2175-81.
    • (2012) Bioorg Med Chem Lett , vol.22 , pp. 2175-2181
    • Song, Z.W.1    Liu, P.2    Yin, W.P.3    Jiang, Y.L.4    Ren, Y.L.5
  • 184
    • 77952987721 scopus 로고    scopus 로고
    • Coumabiocins A-F, aminocoumarins from an organic extract of Streptomyces sp. L-4-4
    • Cheenpracha S, Vidor NB, Yoshida WY, Davies J, Chang LC. Coumabiocins A-F, aminocoumarins from an organic extract of Streptomyces sp. L-4-4. J Nat Prod 2010; 73: 880-4.
    • (2010) J Nat Prod , vol.73 , pp. 880-884
    • Cheenpracha, S.1    Vidor, N.B.2    Yoshida, W.Y.3    Davies, J.4    Chang, L.C.5
  • 185
    • 84874000570 scopus 로고    scopus 로고
    • In vitro antimicrobial and antimycobacterial activity of some chalcones and their derivatives
    • Patel D, Kumari P, Patel NB. In vitro antimicrobial and antimycobacterial activity of some chalcones and their derivatives. Med Chem Res 2013; 22: 726-44.
    • (2013) Med Chem Res , vol.22 , pp. 726-744
    • Patel, D.1    Kumari, P.2    Patel, N.B.3
  • 186
    • 84872014856 scopus 로고    scopus 로고
    • Synthesis of coumarin-based 1,3,4-oxadiazol-2ylthio-N-phenyl/benzothiazolyl acetamides as antimicrobial and antituberculosis agents
    • Patel RV, Kumari P, Rajani DP, Chikhalia KH. Synthesis of coumarin-based 1,3,4-oxadiazol-2ylthio-N-phenyl/benzothiazolyl acetamides as antimicrobial and antituberculosis agents. Med Chem Res 2013; 22: 195-210.
    • (2013) Med Chem Res , vol.22 , pp. 195-210
    • Patel, R.V.1    Kumari, P.2    Rajani, D.P.3    Chikhalia, K.H.4
  • 187
    • 84874000125 scopus 로고    scopus 로고
    • Synthesis and evaluation of antibacterial and antitubercular activities of some novel imidazo[2,1-b][1,3,4]thiadiazole derivatives
    • Joshi SD, Manish K, Badiger A. Synthesis and evaluation of antibacterial and antitubercular activities of some novel imidazo[2,1-b][1,3,4]thiadiazole derivatives. Med Chem Res 2013; 22: 869-78.
    • (2013) Med Chem Res , vol.22 , pp. 869-878
    • Joshi, S.D.1    Manish, K.2    Badiger, A.3
  • 188
    • 77955553615 scopus 로고    scopus 로고
    • Pharmacophores modeling in terms of prediction of theoretical physico-chemical properties and verification by experimental correlations of novel coumarin derivatives produced via Betti's protocol
    • Parvez A, Meshram J, Tiwari V, et al. Pharmacophores modeling in terms of prediction of theoretical physico-chemical properties and verification by experimental correlations of novel coumarin derivatives produced via Betti's protocol. Eur J Med Chem 2010; 45: 4370-8.
    • (2010) Eur J Med Chem , vol.45 , pp. 4370-4378
    • Parvez, A.1    Meshram, J.2    Tiwari, V.3
  • 191
    • 38949088221 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of quinolone-based compounds containing a coumarin moiety
    • Emami S, Foroumadi A, Faramarzi MA, Samadi N. Synthesis and antibacterial activity of quinolone-based compounds containing a coumarin moiety. Arch Pharm Chem Life Sci 2008; 341: 42-8.
    • (2008) Arch Pharm Chem Life Sci , vol.341 , pp. 42-48
    • Emami, S.1    Foroumadi, A.2    Faramarzi, M.A.3    Samadi, N.4
  • 192
    • 48249138451 scopus 로고    scopus 로고
    • Synthesis of some 7-methyl-3-(2-oxo-2H-chromen-3-yl)-5H [1,3]thiazolo[3,2-a]pyrimidin-5-ones
    • Kumar PV, Reddy KM, Rao VR. Synthesis of some 7-methyl-3-(2-oxo-2H-chromen-3-yl)-5H [1,3]thiazolo[3,2-a]pyrimidin-5-ones. Indian J Chem Sect B 2008; 47B: 759-63.
    • (2008) Indian J Chem Sect B , vol.47 B , pp. 759-763
    • Kumar, P.V.1    Reddy, K.M.2    Rao, V.R.3
  • 193
    • 64849088313 scopus 로고    scopus 로고
    • Synthesis of some new coumarin incorporated thiazolyl semicarbazones as anticonvulsants
    • Siddiqui N, Arshad MF, Khan SA. Synthesis of some new coumarin incorporated thiazolyl semicarbazones as anticonvulsants. Acta Pol Pharm 2009; 66: 161-7.
    • (2009) Acta Pol Pharm , vol.66 , pp. 161-167
    • Siddiqui, N.1    Arshad, M.F.2    Khan, S.A.3
  • 194
    • 64949083486 scopus 로고    scopus 로고
    • Synthesis of coumarin linked naphthalimide conjugates as potential anticancer and antimicrobial agents
    • Kamal A, Adil SF, Tamboli JR, Siddardha B, Murthy USN. Synthesis of coumarin linked naphthalimide conjugates as potential anticancer and antimicrobial agents. Lett Drug Des Disc 2009; 6: 201-9.
    • (2009) Lett Drug Des Disc , vol.6 , pp. 201-209
    • Kamal, A.1    Adil, S.F.2    Tamboli, J.R.3    Siddardha, B.4    Murthy, U.S.N.5
  • 196
    • 78649674111 scopus 로고    scopus 로고
    • Synthesis and antihelicobacter pylori activity of 4-(coumarin-3-yl)thiazol-2-ylhydrazone derivatives
    • Chimenti F, Bizzarri B, Bolasco A, et al. Synthesis and antihelicobacter pylori activity of 4-(coumarin-3-yl)thiazol-2-ylhydrazone derivatives. J Heterocycl Chem 2010; 47: 1269-74.
    • (2010) J Heterocycl Chem , vol.47 , pp. 1269-1274
    • Chimenti, F.1    Bizzarri, B.2    Bolasco, A.3
  • 197
    • 79251590274 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of novel 2-(aryl)-3-[5-(2-oxo-2H-3-chromenyl)-1,3-oxazol-2-yl]-1,3-thiazolan-4-ones
    • Reddy CS, Devi MV, Kumar GR, Rao LS, Nagaraj A. Synthesis and antimicrobial activity of novel 2-(aryl)-3-[5-(2-oxo-2H-3-chromenyl)-1,3-oxazol-2-yl]-1,3-thiazolan-4-ones. J Heterocycl Chem 2011; 48: 176-82.
    • (2011) J Heterocycl Chem , vol.48 , pp. 176-182
    • Reddy, C.S.1    Devi, M.V.2    Kumar, G.R.3    Rao, L.S.4    Nagaraj, A.5
  • 198
    • 77955051240 scopus 로고    scopus 로고
    • Synthesis of some new 3-[5-(2-oxo-2H-3-chromenyl)-1,3-oxazol-2-yl]-1,3-thiazolan-4-ones as antimicrobials
    • Reddy CS, Rao LS, Devi MV, Kumar GR, Nagaraj A. Synthesis of some new 3-[5-(2-oxo-2H-3-chromenyl)-1,3-oxazol-2-yl]-1,3-thiazolan-4-ones as antimicrobials. Chin Chem Lett 2010; 21: 1045-8.
    • (2010) Chin Chem Lett , vol.21 , pp. 1045-1048
    • Reddy, C.S.1    Rao, L.S.2    Devi, M.V.3    Kumar, G.R.4    Nagaraj, A.5
  • 199
    • 70449651756 scopus 로고    scopus 로고
    • Synthesis and antimycobacterial activity of N'-[(E)-(mono-substitutedbenzylidene)]-2-pyrazinecarbohydrazide derivatives
    • Vergara FMF, da S Lima CH, Henriques MdasGMdeO, et al. Synthesis and antimycobacterial activity of N'-[(E)-(mono-substitutedbenzylidene)]-2-pyrazinecarbohydrazide derivatives. Eur J Med Chem 2009; 44: 4954-9.
    • (2009) Eur J Med Chem , vol.44 , pp. 4954-4959
    • Vergara, F.M.F.1    Da, S.2    Lima, C.H.3    Henriques MdasGMde, O.4
  • 201
    • 71049120654 scopus 로고    scopus 로고
    • Synthesis and antitubercular activity of 7-chloro-4-quinolinylhydrazones derivatives
    • Candea ALP, Ferreira MdeL, Pais KC, et al. Synthesis and antitubercular activity of 7-chloro-4-quinolinylhydrazones derivatives. Bioorg Med Chem Lett 2009; 19: 6272-4.
    • (2009) Bioorg Med Chem Lett , vol.19 , pp. 6272-6274
    • Candea, A.L.P.1    Ferreira, M.L.2    Pais, K.C.3
  • 203
    • 80052031772 scopus 로고    scopus 로고
    • 7-Hydroxy-coumarin derivatives: Synthesis, characterization and preliminary antimicrobial activities
    • Farshori NN, Banday MR, Ahmad A, Khan AU, Rauf A. 7-Hydroxy-coumarin derivatives: synthesis, characterization and preliminary antimicrobial activities. Med Chem Res 2011; 20: 535-41.
    • (2011) Med Chem Res , vol.20 , pp. 535-541
    • Farshori, N.N.1    Banday, M.R.2    Ahmad, A.3    Khan, A.U.4    Rauf, A.5
  • 204
    • 84866142130 scopus 로고    scopus 로고
    • In vitro antimicrobial assessment of coumarin-based s-triazinyl piperazines
    • Patel D, Patel R, Kumari P, Patel N. In vitro antimicrobial assessment of coumarin-based s-triazinyl piperazines. Med Chem Res 2012; 21: 1611-24.
    • (2012) Med Chem Res , vol.21 , pp. 1611-1624
    • Patel, D.1    Patel, R.2    Kumari, P.3    Patel, N.4
  • 205
    • 84861893596 scopus 로고    scopus 로고
    • Synthesis, characterization, and antimicrobial activity of some new coumarin derivatives
    • Al-Rifai AA, Ayoub MT, Shakya AK, Abu Safleh KA, Mubarak MS. Synthesis, characterization, and antimicrobial activity of some new coumarin derivatives. Med Chem Res 2012; 21: 468-76.
    • (2012) Med Chem Res , vol.21 , pp. 468-476
    • Al-Rifai, A.A.1    Ayoub, M.T.2    Shakya, A.K.3    Abu Safleh, K.A.4    Mubarak, M.S.5
  • 206
    • 54149119357 scopus 로고    scopus 로고
    • Synthesis, anti-tubercular activity and 3D-QSAR study of coumarin-4-acetic acid benzylidene hydrazides
    • Manvar A, Malde A, Verma J, et al. Synthesis, anti-tubercular activity and 3D-QSAR study of coumarin-4-acetic acid benzylidene hydrazides. Eur J Med Chem 2008; 43: 2395-403.
    • (2008) Eur J Med Chem , vol.43 , pp. 2395-2403
    • Manvar, A.1    Malde, A.2    Verma, J.3
  • 207
    • 82955178707 scopus 로고    scopus 로고
    • Synthesis and in-vitro antimycobacterial activity of fluoroquinolone derivatives containing a coumarin moiety
    • Guo Q, Liu ML, Feng LS, et al. Synthesis and in-vitro antimycobacterial activity of fluoroquinolone derivatives containing a coumarin moiety. Arch Pharm Chem Life Sci 2011; 344: 802-9.
    • (2011) Arch Pharm Chem Life Sci , vol.344 , pp. 802-809
    • Guo, Q.1    Liu, M.L.2    Feng, L.S.3
  • 208
    • 77950212862 scopus 로고    scopus 로고
    • Synthesis, in-vitro antimicrobial and cytotoxic studies of novel azetidinone derivatives
    • Keri RS, Hosamani KM, Reddy HS, Shingalapur RV. Synthesis, in-vitro antimicrobial and cytotoxic studies of novel azetidinone derivatives. Arch Pharm Chem Life Sci 2010; 343: 237-47.
    • (2010) Arch Pharm Chem Life Sci , vol.343 , pp. 237-247
    • Keri, R.S.1    Hosamani, K.M.2    Reddy, H.S.3    Shingalapur, R.V.4
  • 210
    • 77954247703 scopus 로고    scopus 로고
    • Design of novel 4-hydroxy-chromene-2-one derivatives as antimicrobial agents
    • Mladenović M, Vuković N, Sukdolak S, Solujić S. Design of novel 4-hydroxy-chromene-2-one derivatives as antimicrobial agents. Molecules 2010; 15: 4294-308.
    • (2010) Molecules , vol.15 , pp. 4294-4308
    • Mladenović, M.1    Vuković, N.2    Sukdolak, S.3    Solujić, S.4
  • 211
    • 72049095332 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of 7-(2-substituted phenylthiazolidinyl)-benzopyran-2-one derivatives
    • Ronad PM, Noolvi MN, Sapkal S, Dharbhamulla S, Maddi VS. Synthesis and antimicrobial activity of 7-(2-substituted phenylthiazolidinyl)-benzopyran-2-one derivatives. Eur J Med Chem 2010; 45: 85-9.
    • (2010) Eur J Med Chem , vol.45 , pp. 85-89
    • Ronad, P.M.1    Noolvi, M.N.2    Sapkal, S.3    Dharbhamulla, S.4    Maddi, V.S.5
  • 212
    • 77955425222 scopus 로고    scopus 로고
    • Synthesis, selective anti-Helicobacter pylori activity, and cytotox of novel N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides
    • Chimenti F, Bizzarri B, Bolasco A, et al. Synthesis, selective anti-Helicobacter pylori activity, and cytotox of novel N-substituted-2-oxo-2H-1-benzopyran-3-carboxamides. Bioorg Med Chem Lett 2010; 20: 4922-6.
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 4922-4926
    • Chimenti, F.1    Bizzarri, B.2    Bolasco, A.3
  • 213
    • 84866403066 scopus 로고    scopus 로고
    • Synthesis, antimicrobial and DNA cleavage studies of some 4-aryloxymethylcoumarins obtained by reaction of 4-bromomethylcoumarins with bidentate nucleophiles
    • Makandar SBN, Basanagouda M, Kulkarni MV, Pranesha, Rasal VP. Synthesis, antimicrobial and DNA cleavage studies of some 4-aryloxymethylcoumarins obtained by reaction of 4-bromomethylcoumarins with bidentate nucleophiles. Med Chem Res 2012; 21: 2603-14.
    • (2012) Med Chem Res , vol.21 , pp. 2603-2614
    • Makandar, S.B.N.1    Basanagouda, M.2    Kulkarni, M.V.3    Pranesha4    Rasal, V.P.5
  • 214
    • 84863230053 scopus 로고    scopus 로고
    • Recent researches in triazole compounds as medicinal drugs
    • Zhou CH, Wang Y. Recent researches in triazole compounds as medicinal drugs. Curr Med Chem 2012; 19: 239-80.
    • (2012) Curr Med Chem , vol.19 , pp. 239-280
    • Zhou, C.H.1    Wang, Y.2
  • 215
    • 84872956673 scopus 로고    scopus 로고
    • Novel berberine triazoles: Synthesis, antimicrobial evaluation and competitive interactions with metal ions to Human Serum Albumin
    • Zhang SL, Chang JJ, Damu GLV, et al. Novel berberine triazoles: synthesis, antimicrobial evaluation and competitive interactions with metal ions to Human Serum Albumin. Bioorg Med Chem Lett 2013; 23: 1008-12.
    • (2013) Bioorg Med Chem Lett , vol.23 , pp. 1008-1012
    • Zhang, S.L.1    Chang, J.J.2    Damu, G.L.V.3
  • 217
    • 79952987722 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of 3-substituted triazole derivatives
    • Wang BG, Yu SC, Chai XY, Yan YZ, Hu HG, Wu QY. Design, synthesis and biological evaluation of 3-substituted triazole derivatives. Chin Chem Lett 2011; 22: 519-22.
    • (2011) Chin Chem Lett , vol.22 , pp. 519-522
    • Wang, B.G.1    Yu, S.C.2    Chai, X.Y.3    Yan, Y.Z.4    Hu, H.G.5    Wu, Q.Y.6
  • 219
    • 78751701180 scopus 로고    scopus 로고
    • Synthesis and evaluation of a class of new coumarin triazole derivatives as potential antimicrobial agents
    • Shi Y, Zhou CH. Synthesis and evaluation of a class of new coumarin triazole derivatives as potential antimicrobial agents. Bioorg Med Chem Lett 2011; 21: 956-60.
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 956-960
    • Shi, Y.1    Zhou, C.H.2
  • 221
    • 79955630008 scopus 로고    scopus 로고
    • Synthesis and pharmacological activity of O-aminoalkyl derivatives of 7-hydroxycoumarin
    • Trykowska Konc J, Hejchman E, Kruszewska H, Wolska I, Maciejewska D. Synthesis and pharmacological activity of O-aminoalkyl derivatives of 7-hydroxycoumarin. Eur J Med Chem 2011; 46: 2252-63.
    • (2011) Eur J Med Chem , vol.46 , pp. 2252-2263
    • Trykowska, K.J.1    Hejchman, E.2    Kruszewska, H.3    Wolska, I.4    McIejewska, D.5
  • 222
    • 76149095981 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of some methyl-2-[N-coumarin-6'-yl]-3-oxo-2,3-dihydro-1H-isoindolone-5-carboxylates
    • Mir AA, Mulwad VV, Trivedi GK. Synthesis and antimicrobial activity of some methyl-2-[N-coumarin-6'-yl]-3-oxo-2,3-dihydro-1H-isoindolone-5-carboxylates. J Heterocycl Chem 2010; 47: 214-8.
    • (2010) J Heterocycl Chem , vol.47 , pp. 214-218
    • Mir, A.A.1    Mulwad, V.V.2    Trivedi, G.K.3
  • 223
    • 62949193424 scopus 로고    scopus 로고
    • A study of the antimicrobial activity of selected naturally occurring and synthetic coumarins
    • Smyth T, Ramachandran VN, Smyth WF. A study of the antimicrobial activity of selected naturally occurring and synthetic coumarins. Int J Antimicrob Agents 2009; 33: 421-6.
    • (2009) Int J Antimicrob Agents , vol.33 , pp. 421-426
    • Smyth, T.1    Ramachandran, V.N.2    Smyth, W.F.3
  • 224
    • 78651102858 scopus 로고    scopus 로고
    • Screening for in vitro antimycobacterial activity and three-dimensional quantitative ttructure-activity relationship (3D-QSAR) study of 4-(arylamino)coumarin derivatives
    • Virsdoia V, Shaikh MS, Manvar A, et al. Screening for in vitro antimycobacterial activity and three-dimensional quantitative ttructure-activity relationship (3D-QSAR) study of 4-(arylamino)coumarin derivatives. Chem Biol Drug Des 2010; 76: 412-24.
    • (2010) Chem Biol Drug Des , vol.76 , pp. 412-424
    • Virsdoia, V.1    Shaikh, M.S.2    Manvar, A.3
  • 225
    • 78650516574 scopus 로고    scopus 로고
    • 3-[Benzimidazo-and 3-[benzothiadiazoleimidazo-(1,2-c)quinazolin-5-yl]-2H-chromene-2-ones as potent antimicrobial agents
    • Kuarm BS, Reddy YT, Madhav JV, Crooks PA, Rajitha B. 3-[Benzimidazo-and 3-[benzothiadiazoleimidazo-(1,2-c)quinazolin-5-yl]-2H-chromene-2-ones as potent antimicrobial agents. Bioorg Med Chem Lett 2011; 21: 524-7.
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 524-527
    • Kuarm, B.S.1    Reddy, Y.T.2    Madhav, J.V.3    Crooks, P.A.4    Rajitha, B.5
  • 226
    • 72149099079 scopus 로고    scopus 로고
    • Design, synthesis and docking studies of new furobenzopyranones and pyranobenzopyranones as photoreagent towards DNA and as antimicrobial agents
    • Farag NAH, El-Tayeb W. Design, synthesis and docking studies of new furobenzopyranones and pyranobenzopyranones as photoreagent towards DNA and as antimicrobial agents. Eur J Med Chem 2010; 45: 317-25.
    • (2010) Eur J Med Chem , vol.45 , pp. 317-325
    • Farag, N.A.H.1    El-Tayeb, W.2
  • 227
    • 77955552724 scopus 로고    scopus 로고
    • Synthesis, structure and DNA cleavage studies of coumarin analogs of tetrahydroisoquinoline and protoberberine alkaloids
    • Jadhav VB, Nayak SK, Row TNG, Kulkarni MV. Synthesis, structure and DNA cleavage studies of coumarin analogs of tetrahydroisoquinoline and protoberberine alkaloids. Eur J Med Chem 2010; 45: 3575-80.
    • (2010) Eur J Med Chem , vol.45 , pp. 3575-3580
    • Jadhav, V.B.1    Nayak, S.K.2    Row, T.N.G.3    Kulkarni, M.V.4
  • 228
    • 84873999734 scopus 로고    scopus 로고
    • Microwave-assisted CAN-catalyzed solvent-free synthesis of N-allyl quinolone-based pyrano[4,3-b]chromene and benzopyrano[3,2-c]chromene derivatives and their antimicrobial activity
    • Jardosh HH, Patel MP. Microwave-assisted CAN-catalyzed solvent-free synthesis of N-allyl quinolone-based pyrano[4,3-b]chromene and benzopyrano[3,2-c]chromene derivatives and their antimicrobial activity. Med Chem Res 2013; 22: 905-15.
    • (2013) Med Chem Res , vol.22 , pp. 905-915
    • Jardosh, H.H.1    Patel, M.P.2
  • 229
    • 78951474787 scopus 로고    scopus 로고
    • Synthesis of novel D-glucosederived benzyl and alkyl 1,2,3-triazoles as potential antifungal and antibacterial agents
    • Wei JJ, Jin L, Wan K, Zhou CH. Synthesis of novel D-glucosederived benzyl and alkyl 1,2,3-triazoles as potential antifungal and antibacterial agents. Bull Korean Chem Soc 2011; 32: 229-38.
    • (2011) Bull Korean Chem Soc , vol.32 , pp. 229-238
    • Wei, J.J.1    Jin, L.2    Wan, K.3    Zhou, C.H.4
  • 230
    • 77956511575 scopus 로고    scopus 로고
    • Polyelectrolyte multilayers fabricated from antifungal β-peptides: Design of surfaces that exhibit antifungal activity against Candida albicans
    • Karlsson AJ, Flessner RM, Gellman SH, Lynn DM, Palecek SP. Polyelectrolyte multilayers fabricated from antifungal β-peptides: design of surfaces that exhibit antifungal activity against Candida albicans. Biomacromolecules 2010; 11: 2321-8.
    • (2010) Biomacromolecules , vol.11 , pp. 2321-2328
    • Karlsson, A.J.1    Flessner, R.M.2    Gellman, S.H.3    Lynn, D.M.4    Palecek, S.P.5
  • 231
    • 79955125453 scopus 로고    scopus 로고
    • Antifungal activity of amphotericin B conjugated to carbon nanotubes
    • Benincasa M, Pacor S, Wu W, Prato M, Bianco A, Gennaro R. Antifungal activity of amphotericin B conjugated to carbon nanotubes. ACS Nano 2011; 5: 199-208.
    • (2011) ACS Nano , vol.5 , pp. 199-208
    • Benincasa, M.1    Pacor, S.2    Wu, W.3    Prato, M.4    Bianco, A.5    Gennaro, R.6
  • 232
    • 80052938876 scopus 로고    scopus 로고
    • Synthesis of novel fluconazoliums and their evaluation for antibacterial and antifungal activities
    • Zhang YY, Mi JL, Zhou CH, Zhou XD. Synthesis of novel fluconazoliums and their evaluation for antibacterial and antifungal activities. Eur J Med Chem 2011; 46: 4391-402.
    • (2011) Eur J Med Chem , vol.46 , pp. 4391-4402
    • Zhang, Y.Y.1    Mi, J.L.2    Zhou, C.H.3    Zhou, X.D.4
  • 234
    • 67650074752 scopus 로고    scopus 로고
    • Synthesis, antibacterial and antifungal activities of novel 1,2,4-triazolium derivatives
    • Luo Y, Lu YH, Gan LL, et al. Synthesis, antibacterial and antifungal activities of novel 1,2,4-triazolium derivatives. Arch Pharm 2009; 342: 386-93.
    • (2009) Arch Pharm , vol.342 , pp. 386-393
    • Luo, Y.1    Lu, Y.H.2    Gan, L.L.3
  • 235
    • 79956145677 scopus 로고    scopus 로고
    • Natural product-based 6-hydroxy-2,3,4,6-tetrahydropyrrolo[1,2-a]pyrimidinium scaffold as a new antifungal template
    • Li XC, Babu KS, Jacob MR, Khan SI, Agarwal AK, Clark AM. Natural product-based 6-hydroxy-2,3,4,6-tetrahydropyrrolo[1,2-a]pyrimidinium scaffold as a new antifungal template. ACS Med Chem Lett 2011; 2: 391-5.
    • (2011) ACS Med Chem Lett , vol.2 , pp. 391-395
    • Li, X.C.1    Babu, K.S.2    Jacob, M.R.3    Khan, S.I.4    Agarwal, A.K.5    Clark, A.M.6
  • 236
    • 84865153151 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of clinafloxacin triazole hybrids as a new type of antibacterial and antifungal agents
    • Wang Y, Damu GLV, Lv JS, Geng RX, Yang DC, Zhou CH. Design, synthesis and evaluation of clinafloxacin triazole hybrids as a new type of antibacterial and antifungal agents. Bioorg Med Chem Lett 2012; 22: 5363-6.
    • (2012) Bioorg Med Chem Lett , vol.22 , pp. 5363-5366
    • Wang, Y.1    Damu, G.L.V.2    Lv, J.S.3    Geng, R.X.4    Yang, D.C.5    Zhou, C.H.6
  • 238
    • 58149195369 scopus 로고    scopus 로고
    • Synthesis and antifungal activity of (Z)-dysidazirine
    • Skepper CK, Dalisay DS, Molinski TF. Synthesis and antifungal activity of (Z)-dysidazirine. Org Lett 2008; 10: 5269-71.
    • (2008) Org Lett , vol.10 , pp. 5269-5271
    • Skepper, C.K.1    Dalisay, D.S.2    Molinski, T.F.3
  • 239
    • 84866434085 scopus 로고    scopus 로고
    • Synthesis of 3-{4-[4-dimethylamino-6-(4-methyl-2-oxo-2H-chromen-7-yloxy)-[1,3,5]triazin-2-ylamino]-phenyl}-2-phenyl-5-(4-pyridin-2-yl-piperazin-1-ylmethyl)-thiazolidin-4-one and their biological evaluation
    • Patel D, Kumari P, Patel N. Synthesis of 3-{4-[4-dimethylamino-6-(4-methyl-2-oxo-2H-chromen-7-yloxy)-[1,3,5]triazin-2-ylamino]-phenyl}-2-phenyl-5-(4-pyridin-2-yl-piperazin-1-ylmethyl)-thiazolidin-4-one and their biological evaluation. Med Chem Res 2012; 21: 2926-44.
    • (2012) Med Chem Res , vol.21 , pp. 2926-2944
    • Patel, D.1    Kumari, P.2    Patel, N.3
  • 240
    • 84873996112 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of coumarin pyrazole pyrimidine 2,4,6(1H,3H,5H)triones and thioxopyrimidine 4,6(1H,5H)diones
    • Vijaya Laxmi S, Suresh Kuarm B, Rajitha B. Synthesis and antimicrobial activity of coumarin pyrazole pyrimidine 2,4,6(1H,3H,5H)triones and thioxopyrimidine 4,6(1H,5H)diones. Med Chem Res 2013; 22: 768-74.
    • (2013) Med Chem Res , vol.22 , pp. 768-774
    • Vijaya Laxmi, S.1    Suresh Kuarm, B.2    Rajitha, B.3
  • 241
    • 39749182754 scopus 로고    scopus 로고
    • Structure-based virtual screening for the discovery of natural inhibitors for human rhinovirus coat protein
    • Rollinger JM, Steindl TM, Schuster D, et al. Structure-based virtual screening for the discovery of natural inhibitors for human rhinovirus coat protein. J Med Chem 2008; 51: 842-51.
    • (2008) J Med Chem , vol.51 , pp. 842-851
    • Rollinger, J.M.1    Steindl, T.M.2    Schuster, D.3
  • 243
    • 84927969172 scopus 로고    scopus 로고
    • Chemical constituents of the roots of Algerian Bunium incrassatum and evaluation of its antimicrobial activity
    • doi: 10.1016/j.arabjc.2011.01.022
    • Bousetla A, Zellagui A, Derouiche K, Rhouati S. Chemical constituents of the roots of Algerian Bunium incrassatum and evaluation of its antimicrobial activity. Arabian J Chem 2011; doi: 10.1016/j.arabjc.2011.01.022.
    • (2011) Arabian J Chem
    • Bousetla, A.1    Zellagui, A.2    Derouiche, K.3    Rhouati, S.4
  • 244
    • 83055160833 scopus 로고    scopus 로고
    • A new antifungal coumarin from Clausena excavate
    • Kumar R, Saha A, Saha D. A new antifungal coumarin from Clausena excavate. Fitoterapia 2012; 83: 230-3.
    • (2012) Fitoterapia , vol.83 , pp. 230-233
    • Kumar, R.1    Saha, A.2    Saha, D.3
  • 245
    • 77954964058 scopus 로고    scopus 로고
    • Antifungal activity of extracts and prenylated coumarins isolated from baccharis darwinii Hook & Arn. (Asteraceae)
    • Kurdelas RR, Lima B, Tapia A, et al. Antifungal activity of extracts and prenylated coumarins isolated from baccharis darwinii Hook & Arn. (Asteraceae). Molecules 2010; 15: 4898-907.
    • (2010) Molecules , vol.15 , pp. 4898-4907
    • Kurdelas, R.R.1    Lima, B.2    Tapia, A.3
  • 248
    • 77955560154 scopus 로고    scopus 로고
    • Synthesis and biological activities of novel amine-derived bis-azoles as potential antibacterial and antifungal agents
    • Fang B, Zhou CH, Rao XC. Synthesis and biological activities of novel amine-derived bis-azoles as potential antibacterial and antifungal agents. Eur J Med Chem 2010; 45: 4388-98.
    • (2010) Eur J Med Chem , vol.45 , pp. 4388-4398
    • Fang, B.1    Zhou, C.H.2    Rao, X.C.3
  • 249
  • 250
    • 79955809921 scopus 로고    scopus 로고
    • Could X-ray analysis explain for the differing antimicrobial and antioxidant activity of two 2-arylamino-3-nitrocoumarins?
    • Radulović NS, Bogdanović GA, Blagojević PD, Dekić VS, Vukicević RD. Could X-ray analysis explain for the differing antimicrobial and antioxidant activity of two 2-arylamino-3-nitrocoumarins? J Chem Crystallogr 2011; 41: 545-51.
    • (2011) J Chem Crystallogr , vol.41 , pp. 545-551
    • Radulović, N.S.1    Bogdanović, G.A.2    Blagojević, P.D.3    Dekić, V.S.4    Vukicević, R.D.5
  • 251
    • 70349542625 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of Schiff's bases of 4-chloro-3-coumarin aldehyde as antimicrobial agents
    • Bairagi S, Bhosale A, Deodhar MN. Design, synthesis and evaluation of Schiff's bases of 4-chloro-3-coumarin aldehyde as antimicrobial agents. E-J Chem 2009; 6: 759-62.
    • (2009) E-J Chem , vol.6 , pp. 759-762
    • Bairagi, S.1    Bhosale, A.2    Deodhar, M.N.3
  • 252
    • 66349085909 scopus 로고    scopus 로고
    • Synthesis and molecular descriptor characterization of novel 4-hydroxy-chromene-2-one derivatives as antimicrobial agents
    • Mladenović M, Vuković N, Nićiforović N, Sukdolak S, Solujić S. Synthesis and molecular descriptor characterization of novel 4-hydroxy-chromene-2-one derivatives as antimicrobial agents. Molecules 2009; 14: 1495-512.
    • (2009) Molecules , vol.14 , pp. 1495-1512
    • Mladenović, M.1    Vuković, N.2    Nićiforović, N.3    Sukdolak, S.4    Solujić, S.5
  • 253
    • 84867217902 scopus 로고    scopus 로고
    • Advance in research of antimicrobial drugs with sulfamide group
    • (in Chinese)
    • Wang XL, Wang XL, Geng RX, Zhou CH. Advance in research of antimicrobial drugs with sulfamide group. Chin J New Drug 2010; 19: 30-9 (in Chinese).
    • (2010) Chin J New Drug , vol.19 , pp. 30-39
    • Wang, X.L.1    Wang, X.L.2    Geng, R.X.3    Zhou, C.H.4
  • 254
    • 79955795774 scopus 로고    scopus 로고
    • Recent advances of 1,2,3-triazole compounds in medicinal chemistry
    • (in Chinese)
    • Wei JJ, Wang Y, Wang XL, Zhou CH, Ji QG. Recent advances of 1,2,3-triazole compounds in medicinal chemistry. Chin Pharm J 2011; 46: 481-5 (in Chinese).
    • (2011) Chin Pharm J , vol.46 , pp. 481-485
    • Wei, J.J.1    Wang, Y.2    Wang, X.L.3    Zhou, C.H.4    Ji, Q.G.5
  • 255
    • 77956186207 scopus 로고    scopus 로고
    • Synthesis of novel sulfanilamidederived 1,2,3-triazoles and their evaluation for antibacterial and antifungal activities
    • Wang XL, Wan K, Zhou CH. Synthesis of novel sulfanilamidederived 1,2,3-triazoles and their evaluation for antibacterial and antifungal activities. Eur J Med Chem 2010; 45: 4631-9.
    • (2010) Eur J Med Chem , vol.45 , pp. 4631-4639
    • Wang, X.L.1    Wan, K.2    Zhou, C.H.3
  • 256
    • 77950241664 scopus 로고    scopus 로고
    • Copper-mediated N-heteroarylation of primary sulfonamides: Synthesis of mono-N-heteroaryl sulfonamides
    • Baffoe J, Hoe MY, Toure BB. Copper-mediated N-heteroarylation of primary sulfonamides: synthesis of mono-N-heteroaryl sulfonamides. Org Lett 2010; 12: 1532-5.
    • (2010) Org Lett , vol.12 , pp. 1532-1535
    • Baffoe, J.1    Hoe, M.Y.2    Toure, B.B.3
  • 258
    • 75849128571 scopus 로고    scopus 로고
    • Synthesis and antimicrobial studies on novel sulfonamides containing 4-azidomethyl coumarin
    • Basanagouda M, Shivashankar K, Kulkarni MV, et al. Synthesis and antimicrobial studies on novel sulfonamides containing 4-azidomethyl coumarin. Eur J Med Chem 2010; 45: 1151-7.
    • (2010) Eur J Med Chem , vol.45 , pp. 1151-1157
    • Basanagouda, M.1    Shivashankar, K.2    Kulkarni, M.V.3
  • 259
    • 77953156366 scopus 로고    scopus 로고
    • Synthesis, characterization and antimicrobial properties of Schiff bases derived from condensation of 8-formyl-7-hydroxy-4-methylcoumarin and substituted triazole derivatives
    • Lamani KSS, Kotresh O, Phaniband MA, Kadakol JC. Synthesis, characterization and antimicrobial properties of Schiff bases derived from condensation of 8-formyl-7-hydroxy-4-methylcoumarin and substituted triazole derivatives. E-J Chem 2009; 6: S239-46.
    • (2009) E-J Chem , vol.6
    • Lamani, K.S.S.1    Kotresh, O.2    Phaniband, M.A.3    Kadakol, J.C.4
  • 260
    • 78649931835 scopus 로고    scopus 로고
    • What makes Aspergillus fumigatus a successful pathogen? Genes and molecules involved in invasive aspergillosis
    • Abad A, Fernández-Molina JV, Bikandi J, et al. What makes Aspergillus fumigatus a successful pathogen? Genes and molecules involved in invasive aspergillosis. Rev Iberoam Micol 2010; 27: 155-82.
    • (2010) Rev Iberoam Micol , vol.27 , pp. 155-182
    • Abad, A.1    Fernández-Molina, J.V.2    Bikandi, J.3
  • 261
    • 62149144052 scopus 로고    scopus 로고
    • Allergic bronchopulmonary aspergillosis
    • Agarwal R. Allergic bronchopulmonary aspergillosis. Chest 2009; 135: 805-26.
    • (2009) Chest , vol.135 , pp. 805-826
    • Agarwal, R.1
  • 262
    • 84861801730 scopus 로고    scopus 로고
    • Proteomic characterization of Aspergillus fumigatus treated with an antifungal coumarin for identification of novel target molecules of key pathways
    • Singh S, Gupta S, Singh B, Sharma SK, Gupta VK, Sharma GL. Proteomic characterization of Aspergillus fumigatus treated with an antifungal coumarin for identification of novel target molecules of key pathways. J Proteome Res 2012; 11: 3259-68.
    • (2012) J Proteome Res , vol.11 , pp. 3259-3268
    • Singh, S.1    Gupta, S.2    Singh, B.3    Sharma, S.K.4    Gupta, V.K.5    Sharma, G.L.6
  • 263
    • 84866403066 scopus 로고    scopus 로고
    • Synthesis, antimicrobial and DNA cleavage studies of some 4-aryloxymethylcoumarins obtained by reaction of 4-bromomethylcoumarins with bidentate nucleophiles
    • Makandar SBN, Basanagouda M, Kulkarni MV, Pranesha, Rasal VP. Synthesis, antimicrobial and DNA cleavage studies of some 4-aryloxymethylcoumarins obtained by reaction of 4-bromomethylcoumarins with bidentate nucleophiles. Med Chem Res 2012; 21: 2603-14.
    • (2012) Med Chem Res , vol.21 , pp. 2603-2614
    • Makandar, S.B.N.1    Basanagouda, M.2    Kulkarni, M.V.3    Pranesha4    Rasal, V.P.5
  • 264
    • 84872007470 scopus 로고    scopus 로고
    • Solvent-and catalyst-free synthesis of bis-adducts of 3-formylchromone as potential antimicrobial agents
    • Siddiqui ZN, Musthafa TNM, Praveen S. Solvent-and catalyst-free synthesis of bis-adducts of 3-formylchromone as potential antimicrobial agents. Med Chem Res 2013; 22: 127-33.
    • (2013) Med Chem Res , vol.22 , pp. 127-133
    • Siddiqui, Z.N.1    Musthafa, T.N.M.2    Praveen, S.3
  • 265
    • 67650237637 scopus 로고    scopus 로고
    • 7-Omethylkaempferol and-quercetin Glycosides from the whole plant of Nervilia fordii
    • Tian LW, Pei Y, Zhang YJ, Wang YF, Yang CR. 7-Omethylkaempferol and-quercetin Glycosides from the whole plant of Nervilia fordii. J Nat Prod 2009; 72: 1057-60.
    • (2009) J Nat Prod , vol.72 , pp. 1057-1060
    • Tian, L.W.1    Pei, Y.2    Zhang, Y.J.3    Wang, Y.F.4    Yang, C.R.5
  • 266
    • 79960785044 scopus 로고    scopus 로고
    • Benzylidene-bis-(4-Hydroxycoumarin) and benzopyrano-coumarin derivatives: Synthesis, 1H/13C-NMR conformational and X-ray crystal structure studies and in vitro antiviral activity evaluations
    • Završnik D, Muratoviš S, Makuc D, et al. Benzylidene-bis-(4-Hydroxycoumarin) and benzopyrano-coumarin derivatives: synthesis, 1H/13C-NMR conformational and X-ray crystal structure studies and in vitro antiviral activity evaluations. Molecules 2011; 16: 6023-40.
    • (2011) Molecules , vol.16 , pp. 6023-6040
    • Završnik, D.1    Muratoviš, S.2    Makuc, D.3
  • 267
    • 52749083185 scopus 로고    scopus 로고
    • Advances in the research of the macrocyclic agents
    • (in Chinese)
    • Yu KG, Zhou CH, Li DH. Advances in the research of the macrocyclic agents. Chin Pharm J 2008; 43: 481-8 (in Chinese).
    • (2008) Chin Pharm J , vol.43 , pp. 481-488
    • Yu, K.G.1    Zhou, C.H.2    Li, D.H.3
  • 268
    • 39849110713 scopus 로고    scopus 로고
    • Hepatitis C virus (HCV) infection: A systemic disease
    • Craxi A, Laffi G, Zignego AL. Hepatitis C virus (HCV) infection: a systemic disease. Mol Aspects Med 2008; 29: 85-95.
    • (2008) Mol Aspects Med , vol.29 , pp. 85-95
    • Craxi, A.1    Laffi, G.2    Zignego, A.L.3
  • 269
    • 38149026447 scopus 로고    scopus 로고
    • Synthesis of new benzimidazole-coumarin conjugates as anti-hepatitis C virus agents
    • Hwu JR, Singha R, Hong SC, et al. Synthesis of new benzimidazole-coumarin conjugates as anti-hepatitis C virus agents. Antivir Res 2008; 77: 157-62.
    • (2008) Antivir Res , vol.77 , pp. 157-162
    • Hwu, J.R.1    Singha, R.2    Hong, S.C.3
  • 270
    • 64349103355 scopus 로고    scopus 로고
    • Structure activity relationship of new anti-hepatitis C virus agents: Heterobicycle coumarin conjugates
    • Neyts J, Clercq ED, Singha R, et al. Structure activity relationship of new anti-hepatitis C virus agents: heterobicycle coumarin conjugates. J Med Chem 2009; 52: 1486-90.
    • (2009) J Med Chem , vol.52 , pp. 1486-1490
    • Neyts, J.1    Clercq, E.D.2    Singha, R.3
  • 271
    • 79953776648 scopus 로고    scopus 로고
    • Coumarin-purine ribofuranoside conjugates as new agents against hepatitis C virus
    • Hwu JR, Lin SY, Tsay SC, Clercq ED, Leyssen P, Neyts J. Coumarin-purine ribofuranoside conjugates as new agents against hepatitis C virus. J Med Chem 2011; 54: 2114-26.
    • (2011) J Med Chem , vol.54 , pp. 2114-2126
    • Hwu, J.R.1    Lin, S.Y.2    Tsay, S.C.3    Clercq, E.D.4    Leyssen, P.5    Neyts, J.6
  • 272
    • 40749146330 scopus 로고    scopus 로고
    • Synthesis of Mannich bases of 7-hydroxycoumarin and screened against Flaviviridae
    • Mazzei M, Nieddu E, Miele M, et al. Synthesis of Mannich bases of 7-hydroxycoumarin and screened against Flaviviridae. Bioorg Med Chem 2008; 16: 2591-605.
    • (2008) Bioorg Med Chem , vol.16 , pp. 2591-2605
    • Mazzei, M.1    Nieddu, E.2    Miele, M.3
  • 273
    • 41749084640 scopus 로고    scopus 로고
    • Chemical library and structure-activity relationships of 11-demethyl-12-oxo calanolide A analogs as anti-HIV-1 agents
    • Ma T, Liu L, Xue H, et al. Chemical library and structure-activity relationships of 11-demethyl-12-oxo calanolide A analogs as anti-HIV-1 agents. J Med Chem 2008; 51: 1432-46.
    • (2008) J Med Chem , vol.51 , pp. 1432-1446
    • Ma, T.1    Liu, L.2    Xue, H.3
  • 274
    • 77249123906 scopus 로고    scopus 로고
    • Highly suppressing wild-type HIV-1 and Y181C mutant HIV-1 strains by 10-chloromethyl-11-demethyl-12-oxo-calanolide A with druggable profile
    • Xue H, Lu XF, Zheng PR, et al. Highly suppressing wild-type HIV-1 and Y181C mutant HIV-1 strains by 10-chloromethyl-11-demethyl-12-oxo-calanolide A with druggable profile. J Med Chem 2010; 53: 1397-401.
    • (2010) J Med Chem , vol.53 , pp. 1397-1401
    • Xue, H.1    Lu, X.F.2    Zheng, P.R.3
  • 275
    • 66349109052 scopus 로고    scopus 로고
    • Synthesis and studies of new 2-(coumarin-4-yloxy)-4,6-(substituted)-striazine derivatives as potential anti-HIV agents
    • Mahajan DH, Pannecouque C, Clercq ED, Chikhalia KH. Synthesis and studies of new 2-(coumarin-4-yloxy)-4,6-(substituted)-striazine derivatives as potential anti-HIV agents. Arch Pharm Chem Life Sci 2009; 342: 281-90.
    • (2009) Arch Pharm Chem Life Sci , vol.342 , pp. 281-290
    • Mahajan, D.H.1    Pannecouque, C.2    Clercq, E.D.3    Chikhalia, K.H.4
  • 276
    • 67249138142 scopus 로고    scopus 로고
    • Pandemic potential of a strain of influenzaA(H1N1): Early findings
    • Fraser C, Donnelly CA, Cauchemez S, et al. Pandemic potential of a strain of influenzaA(H1N1): early findings. Science 2009; 324: 1557-61.
    • (2009) Science , vol.324 , pp. 1557-1561
    • Fraser, C.1    Donnelly, C.A.2    Cauchemez, S.3
  • 277
    • 40349106180 scopus 로고    scopus 로고
    • Cancer chemopreventive activity of terpenoid coumarins from Ferula species
    • Iranshahi M, Kalategi F, Rezaee R, et al. Cancer chemopreventive activity of terpenoid coumarins from Ferula species. Planta Med 2008; 74: 147-50.
    • (2008) Planta Med , vol.74 , pp. 147-150
    • Iranshahi, M.1    Kalategi, F.2    Rezaee, R.3
  • 278
    • 70349513459 scopus 로고    scopus 로고
    • 1) antiviral and cytotoxic agents from Ferula assa-foetida
    • 1) antiviral and cytotoxic agents from Ferula assa-foetida. J Nat Prod 2009; 72: 1568-72.
    • (2009) J Nat Prod , vol.72 , pp. 1568-1572
    • Lee, C.L.1    Chiang, L.C.2    Cheng, L.H.3
  • 279
    • 77649210704 scopus 로고    scopus 로고
    • Anti-influenza drug discovery: Structure-activity relationship and mechanistic insight into novel angelicin derivatives
    • Yeh JY, Coumar MS, Horng JT, et al. Anti-influenza drug discovery: structure-activity relationship and mechanistic insight into novel angelicin derivatives. J Med Chem 2010; 53: 1519-33.
    • (2010) J Med Chem , vol.53 , pp. 1519-1533
    • Yeh, J.Y.1    Coumar, M.S.2    Horng, J.T.3
  • 280
    • 77953017254 scopus 로고    scopus 로고
    • Coumarins from Galipea Panamensis and their activity against Leishmania Panamensis
    • Arango V, Robledo S, Séon-Méniel B, et al. Coumarins from Galipea Panamensis and their activity against Leishmania Panamensis. J Nat Prod 2010; 73: 1012-4.
    • (2010) J Nat Prod , vol.73 , pp. 1012-1014
    • Arango, V.1    Robledo, S.2    Séon-Méniel, B.3
  • 281
    • 76749136619 scopus 로고    scopus 로고
    • Antileishmanial activity of furoquinolines and coumarins from Helietta apiculata
    • Ferreira ME, Arias ARD, Yaluff G, et al. Antileishmanial activity of furoquinolines and coumarins from Helietta apiculata. Phytomedicine 2010; 17: 375-8.
    • (2010) Phytomedicine , vol.17 , pp. 375-378
    • Ferreira, M.E.1    Arias, A.R.D.2    Yaluff, G.3
  • 282
    • 54049094332 scopus 로고    scopus 로고
    • Structureactivity relationship of (-) mammea A/BB derivatives against Leishmania amazonensis
    • Brenzan MA, Nakamura CV, Dias Filho BP, et al. Structureactivity relationship of (-) mammea A/BB derivatives against Leishmania amazonensis. Biomed Pharmacother 2008; 62: 651-8.
    • (2008) Biomed Pharmacother , vol.62 , pp. 651-658
    • Brenzan, M.A.1    Nakamura, C.V.2    Dias Filho, B.P.3
  • 283
    • 76049098694 scopus 로고    scopus 로고
    • Synthesis and antiprotozoal activity of 4-arylcoumarins
    • Pierson JT, Dumètre A, Hutter S, et al. Synthesis and antiprotozoal activity of 4-arylcoumarins. Eur J Med Chem 2010; 45: 864-9.
    • (2010) Eur J Med Chem , vol.45 , pp. 864-869
    • Pierson, J.T.1    Dumètre, A.2    Hutter, S.3
  • 284
    • 55349093261 scopus 로고    scopus 로고
    • Drug resistance and genetic mapping in Plasmodium falciparum
    • Hayton K, Su XZ. Drug resistance and genetic mapping in Plasmodium falciparum. Curr Genet 2008; 54: 223-9.
    • (2008) Curr Genet , vol.54 , pp. 223-229
    • Hayton, K.1    Su, X.Z.2
  • 285
    • 56249098367 scopus 로고    scopus 로고
    • Selection of a trioxaquine as an antimalarial drug candidate
    • Coslédan F, Fraisse L, Pellet A, et al. Selection of a trioxaquine as an antimalarial drug candidate. Proc Natl Acad Sci USA 2008; 105: 17579-84.
    • (2008) Proc Natl Acad Sci USA , vol.105 , pp. 17579-17584
    • Coslédan, F.1    Fraisse, L.2    Pellet, A.3
  • 286
    • 84861575644 scopus 로고    scopus 로고
    • Coumarin-trioxane hybrids: Synthesis and evaluation as a new class of antimalarial scaffolds
    • Sashidhara KV, Kumar A, Dodda RP, et al. Coumarin-trioxane hybrids: synthesis and evaluation as a new class of antimalarial scaffolds. Bioorg Med Chem Lett 2012; 22: 3926-30.
    • (2012) Bioorg Med Chem Lett , vol.22 , pp. 3926-3930
    • Sashidhara, K.V.1    Kumar, A.2    Dodda, R.P.3
  • 287
    • 84861232297 scopus 로고    scopus 로고
    • De novo design of 7-aminocoumarin derivatives as novel falcipain-3 inhibitors
    • Chintakrindi AS, Shaikh MS, Coutinho EC. De novo design of 7-aminocoumarin derivatives as novel falcipain-3 inhibitors. J Mol Model 2012; 18: 1481-93.
    • (2012) J Mol Model , vol.18 , pp. 1481-1493
    • Chintakrindi, A.S.1    Shaikh, M.S.2    Coutinho, E.C.3
  • 288
    • 84866054168 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of some novel 3-cinnamoyl-4-hydroxy-2H-chromen-2-ones as antimalarial agents
    • Patel K, Karthikeyan C, Moorthy NSHN, et al. Design, synthesis and biological evaluation of some novel 3-cinnamoyl-4-hydroxy-2H-chromen-2-ones as antimalarial agents. Med Chem Res 2012; 21: 1780-4.
    • (2012) Med Chem Res , vol.21 , pp. 1780-1784
    • Patel, K.1    Karthikeyan, C.2    Moorthy, N.S.H.N.3
  • 289
    • 62549091389 scopus 로고    scopus 로고
    • Antiamoebic coumarins from the root bark of Adina cordifolia and their new thiosemicarbazone derivatives
    • Iqbal PF, Bhat AR, Azam A. Antiamoebic coumarins from the root bark of Adina cordifolia and their new thiosemicarbazone derivatives. Eur J Med Chem 2009; 44: 2252-9.
    • (2009) Eur J Med Chem , vol.44 , pp. 2252-2259
    • Iqbal, P.F.1    Bhat, A.R.2    Azam, A.3
  • 290
    • 79955398108 scopus 로고    scopus 로고
    • Mechanisms involved in the antinociceptive effects of 7-hydroxycoumarin
    • Oliveira de Lima F, Nonato FR, Couto RD, et al. Mechanisms involved in the antinociceptive effects of 7-hydroxycoumarin. J Nat Prod 2011; 74: 596-602.
    • (2011) J Nat Prod , vol.74 , pp. 596-602
    • de Oliveira Lima, F.1    Nonato, F.R.2    Couto, R.D.3
  • 291
    • 84863377867 scopus 로고    scopus 로고
    • Recent advances in syntheses of oxazole compounds
    • (in Chinese)
    • Zhang HZ, Zhou CH, Geng RX, Ji QG. Recent advances in syntheses of oxazole compounds. Chin J Org Chem 2011; 31: 1963-76 (in Chinese).
    • (2011) Chin J Org Chem , vol.31 , pp. 1963-1976
    • Zhang, H.Z.1    Zhou, C.H.2    Geng, R.X.3    Ji, Q.G.4
  • 292
    • 77949809473 scopus 로고    scopus 로고
    • Synthesis, spectral, thermal analysis, biological activity and kinetic studies of copper (II)-pyradine-2,5-dicarboxylate complexes with 2-aminomethylpyridine and 8-hydroxyquinoline
    • Çolak AT, Çolak F, Atar N, Olgun A. Synthesis, spectral, thermal analysis, biological activity and kinetic studies of copper (II)-pyradine-2,5-dicarboxylate complexes with 2-aminomethylpyridine and 8-hydroxyquinoline. Acta Chim Slov 2010; 57: 212-21.
    • (2010) Acta Chim Slov , vol.57 , pp. 212-221
    • Çolak, A.T.1    Çolak, F.2    Atar, N.3    Olgun, A.4
  • 293
    • 70349425876 scopus 로고    scopus 로고
    • Synthesis and C6-ethylidene meropenem derivative with antimicrobial activity
    • Anderluh PŠ, Vilfan G, Prezelj A, Urleb U. Synthesis and C6-ethylidene meropenem derivative with antimicrobial activity. Acta Chim Slov 2009; 56: 669-73.
    • (2009) Acta Chim Slov , vol.56 , pp. 669-673
    • Anderluh, P.S.1    Vilfan, G.2    Prezelj, A.3    Urleb, U.4
  • 294
    • 68649089712 scopus 로고    scopus 로고
    • Anti-inflammatory effect of coumarins isolated from Corydalis heterocarpa in HT-29 human colon carcinoma cells
    • Kang KH, Kong CS, Seo Y, Kim MM, Kim SK. Anti-inflammatory effect of coumarins isolated from Corydalis heterocarpa in HT-29 human colon carcinoma cells. Food Chem Toxicol 2009; 47: 2129-34.
    • (2009) Food Chem Toxicol , vol.47 , pp. 2129-2134
    • Kang, K.H.1    Kong, C.S.2    Seo, Y.3    Kim, M.M.4    Kim, S.K.5
  • 295
    • 78049415217 scopus 로고    scopus 로고
    • Antiinflammatory activity of coumarins from Ligusticum lucidum Mill. subsp. cuneifolium (Guss.) Tammaro (Apiaceae)
    • Menghini L, Epifano F, Genovese S, Marcotullio MC, Sosa S, Tubaro A. Antiinflammatory activity of coumarins from Ligusticum lucidum Mill. subsp. cuneifolium (Guss.) Tammaro (Apiaceae). Phytother Res 2010; 24: 1697-9.
    • (2010) Phytother Res , vol.24 , pp. 1697-1699
    • Menghini, L.1    Epifano, F.2    Genovese, S.3    Marcotullio, M.C.4    Sosa, S.5    Tubaro, A.6
  • 296
    • 80052946240 scopus 로고    scopus 로고
    • Synthesis, pharmacological evaluation and docking studies of coumarin derivatives
    • Sandhya B, Giles D, Mathew V, Basavarajaswamy G, Abraham R. Synthesis, pharmacological evaluation and docking studies of coumarin derivatives. Eur J Med Chem 2011; 46: 4696-701.
    • (2011) Eur J Med Chem , vol.46 , pp. 4696-4701
    • Sandhya, B.1    Giles, D.2    Mathew, V.3    Basavarajaswamy, G.4    Abraham, R.5
  • 297
    • 61349181828 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of a novel series of 5-(substituted) aryl-3-(3-coumarinyl)-1-phenyl-2-pyrazolines as novel anti-inflammatory and analgesic agents
    • Khode S, Maddi V, Aragade P, et al. Synthesis and pharmacological evaluation of a novel series of 5-(substituted) aryl-3-(3-coumarinyl)-1-phenyl-2-pyrazolines as novel anti-inflammatory and analgesic agents. Eur J Med Chem 2009; 44: 1682-8.
    • (2009) Eur J Med Chem , vol.44 , pp. 1682-1688
    • Khode, S.1    Maddi, V.2    Aragade, P.3
  • 298
    • 67650264156 scopus 로고    scopus 로고
    • Synthesis, biological evaluation and docking studies of novel benzopyranone congeners for their expected activity as anti-inflammatory, analgesic and antipyretic agents
    • Eissa AAM, Farag NAH, Soliman GAH. Synthesis, biological evaluation and docking studies of novel benzopyranone congeners for their expected activity as anti-inflammatory, analgesic and antipyretic agents. Bioorg Med Chem 2009; 17: 5059-70.
    • (2009) Bioorg Med Chem , vol.17 , pp. 5059-5070
    • Eissa, A.A.M.1    Farag, N.A.H.2    Soliman, G.A.H.3
  • 299
    • 77950860382 scopus 로고    scopus 로고
    • Analgesic, anti-pyretic and DNA cleavage studies of novel pyrimidine derivatives of coumarin moiety
    • Keri RS, Hosamani KM, Shingalapur RV, Hugar MH. Analgesic, anti-pyretic and DNA cleavage studies of novel pyrimidine derivatives of coumarin moiety. Eur J Med Chem 2010; 45: 2597-605.
    • (2010) Eur J Med Chem , vol.45 , pp. 2597-2605
    • Keri, R.S.1    Hosamani, K.M.2    Shingalapur, R.V.3    Hugar, M.H.4
  • 300
    • 84866098913 scopus 로고    scopus 로고
    • Analgesic study of novel pyrimidine derivatives linked with coumarin moiety
    • Gupta JK, Sharma PK, Dudhe R, et al. Analgesic study of novel pyrimidine derivatives linked with coumarin moiety. Med Chem Res 2012; 21: 1625-32.
    • (2012) Med Chem Res , vol.21 , pp. 1625-1632
    • Gupta, J.K.1    Sharma, P.K.2    Dudhe, R.3
  • 302
    • 84856219861 scopus 로고    scopus 로고
    • Synthesis and evaluation of anti-inflammatory and analgesic activity of 3-[(5-substituted-1,3,4-oxadiazol-2-yl-thio)acetyl]-2H-chromen-2-ones
    • Ingale N, Maddi V, Palkar M, et al. Synthesis and evaluation of anti-inflammatory and analgesic activity of 3-[(5-substituted-1,3,4-oxadiazol-2-yl-thio)acetyl]-2H-chromen-2-ones. Med Chem Res 2012; 21: 16-26.
    • (2012) Med Chem Res , vol.21 , pp. 16-26
    • Ingale, N.1    Maddi, V.2    Palkar, M.3
  • 303
    • 77649197278 scopus 로고    scopus 로고
    • Discovery and optimization of novel 3-piperazinylcoumarin antagonist of chemokine-like factor 1 with oral antiasthma activity in mice
    • Li G., Wang DM, Sun MN, et al. Discovery and optimization of novel 3-piperazinylcoumarin antagonist of chemokine-like factor 1 with oral antiasthma activity in mice. J Med Chem 2010; 53: 1741-54.
    • (2010) J Med Chem , vol.53 , pp. 1741-1754
    • Li, G.1    Wang, D.M.2    Sun, M.N.3
  • 304
    • 79956194835 scopus 로고    scopus 로고
    • Effect of compound IMMLG5521, a novel coumarin derivative, on carrageenan-induced pleurisy in rats
    • Li ZP, Hu JF, Sun MN, et al. Effect of compound IMMLG5521, a novel coumarin derivative, on carrageenan-induced pleurisy in rats. Eur J Pharmacol 2011; 661: 118-23.
    • (2011) Eur J Pharmacol , vol.661 , pp. 118-123
    • Li, Z.P.1    Hu, J.F.2    Sun, M.N.3
  • 305
    • 84864044803 scopus 로고    scopus 로고
    • Anti-inflammatory effect of IMMLG5521, a coumarin derivative, on sephadex-induced lung inflammation in rats
    • Li ZP, Hu JF, Sun MN, et al. Anti-inflammatory effect of IMMLG5521, a coumarin derivative, on sephadex-induced lung inflammation in rats. Int Immunopharm 2012; 14: 145-9.
    • (2012) Int Immunopharm , vol.14 , pp. 145-149
    • Li, Z.P.1    Hu, J.F.2    Sun, M.N.3
  • 306
    • 84862219770 scopus 로고    scopus 로고
    • New coumarins and antiin flammatory constituents from Zanthoxylum avicennae
    • Cho JY, Hwang TL, Chang TH, et al. New coumarins and antiin flammatory constituents from Zanthoxylum avicennae. Food Chem 2012; 135: 17-23.
    • (2012) Food Chem , vol.135 , pp. 17-23
    • Cho, J.Y.1    Hwang, T.L.2    Chang, T.H.3
  • 307
    • 84864694567 scopus 로고    scopus 로고
    • Anti-inflammatory new coumarin from the Ammi majus L
    • Selim YA, Ouf NH. Anti-inflammatory new coumarin from the Ammi majus L. Org Med Chem Lett 2012; 2: 1-4.
    • (2012) Org Med Chem Lett , vol.2 , pp. 1-4
    • Selim, Y.A.1    Ouf, N.H.2
  • 308
    • 80052946717 scopus 로고    scopus 로고
    • Synthesis and antiin flammatory effects of a series of novel 7-hydroxycoumarin derivatives
    • Timonen JM, Nieminen RM, Sareila O, et al. Synthesis and antiin flammatory effects of a series of novel 7-hydroxycoumarin derivatives. Eur J Med Chem 2011; 46: 3845-50.
    • (2011) Eur J Med Chem , vol.46 , pp. 3845-3850
    • Timonen, J.M.1    Nieminen, R.M.2    Sareila, O.3
  • 309
    • 62949184168 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of coumarin derivatives as cannabinoid receptor antagonists and inverse agonists
    • Behrenswerth A, Volz N, Toräng J, Hinz S, Bräse S, Müller CE. Synthesis and pharmacological evaluation of coumarin derivatives as cannabinoid receptor antagonists and inverse agonists. Bioorg Med Chem 2009; 17: 2842-51.
    • (2009) Bioorg Med Chem , vol.17 , pp. 2842-2851
    • Behrenswerth, A.1    Volz, N.2    Toräng, J.3    Hinz, S.4    Bräse, S.5    Müller, C.E.6
  • 311
    • 73749087813 scopus 로고    scopus 로고
    • Design, synthesis and anti-inflammatory evaluation of PEGylated 4-methyl and 4,8-dimethylcoumarins
    • Pandey MK, Balwani S, Sharma PK, Parmar VS, Ghosh B, Watterson AC. Design, synthesis and anti-inflammatory evaluation of PEGylated 4-methyl and 4,8-dimethylcoumarins. Eur J Pharm Sci 2010; 39: 134-40.
    • (2010) Eur J Pharm Sci , vol.39 , pp. 134-140
    • Pandey, M.K.1    Balwani, S.2    Sharma, P.K.3    Parmar, V.S.4    Ghosh, B.5    Watterson, A.C.6
  • 312
    • 77954507691 scopus 로고    scopus 로고
    • Biological activity of the chemical constituents from Clausena harmandiana
    • Thongthoom T, Songsiang U, Phaosiri C, Yenjai C. Biological activity of the chemical constituents from Clausena harmandiana. Arch Pharm Res 2010; 33: 675-80.
    • (2010) Arch Pharm Res , vol.33 , pp. 675-680
    • Thongthoom, T.1    Songsiang, U.2    Phaosiri, C.3    Yenjai, C.4
  • 314
  • 315
    • 79956189293 scopus 로고    scopus 로고
    • Synthesis of 3-aryl-4-({2-[4-(6-substituted-coumarin-3-yl)-1,3-thiazol-2-yl]hydrazinylidene}methyl/ethyl)-sydnones using silica sulfuric acid and their antidiabetic, DNA cleavage activity
    • doi: 10.1016/j.arabjc.2011.04.006
    • Tegginamath G, Kamble RR, Kattimani PP, Margankop SB. Synthesis of 3-aryl-4-({2-[4-(6-substituted-coumarin-3-yl)-1,3-thiazol-2-yl]hydrazinylidene}methyl/ethyl)-sydnones using silica sulfuric acid and their antidiabetic, DNA cleavage activity. Arabian J Chem 2011; doi: 10.1016/j.arabjc.2011.04.006.
    • (2011) Arabian J Chem
    • Tegginamath, G.1    Kamble, R.R.2    Kattimani, P.P.3    Margankop, S.B.4
  • 316
    • 77953870862 scopus 로고    scopus 로고
    • Synthesis and biological activity of glycosyl-1H-1,2,3-triazoles
    • Slamova K, Marhol P, Bezouska K, et al. Synthesis and biological activity of glycosyl-1H-1,2,3-triazoles. Bioorg Med Chem Lett 2010; 20: 4263-5.
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 4263-4265
    • Slamova, K.1    Marhol, P.2    Bezouska, K.3
  • 317
    • 77949838793 scopus 로고    scopus 로고
    • Synthesis, biological activity, and molecular modeling studies of 1H-1,2,3-triazole derivatives of carbohydrates as α-glucosidase inhibitors
    • Ferreira SB, Sodero ACR, Cardoso MFC, et al. Synthesis, biological activity, and molecular modeling studies of 1H-1,2,3-triazole derivatives of carbohydrates as α-glucosidase inhibitors. J Med Chem 2010; 53: 2364-74.
    • (2010) J Med Chem , vol.53 , pp. 2364-2374
    • Ferreira, S.B.1    Sodero, A.C.R.2    Cardoso, M.F.C.3
  • 318
    • 78650180739 scopus 로고    scopus 로고
    • Application of click chemistry towards an effcient synthesis of 1,2,3-1H-triazolyl glycohybrids as enzyme inhibitors
    • Anand N, Jaiswal N, Pandey SK, Srivastava AK, Tripathi RP. Application of click chemistry towards an effcient synthesis of 1,2,3-1H-triazolyl glycohybrids as enzyme inhibitors. Carbohydr Res 2011; 346: 16-25.
    • (2011) Carbohydr Res , vol.346 , pp. 16-25
    • Anand, N.1    Jaiswal, N.2    Pandey, S.K.3    Srivastava, A.K.4    Tripathi, R.P.5
  • 319
    • 79951630832 scopus 로고    scopus 로고
    • Synthesis and oral hypoglycemic activity of 3-[5'-methyl-2'-aryl-3'-(thiazol-2''-yl amino) thiazolidin-4'-one]coumarin derivatives
    • Kini D, Ghate M. Synthesis and oral hypoglycemic activity of 3-[5'-methyl-2'-aryl-3'-(thiazol-2''-yl amino) thiazolidin-4'-one]coumarin derivatives. E-J Chem 2011; 8: 386-90.
    • (2011) E-J Chem , vol.8 , pp. 386-390
    • Kini, D.1    Ghate, M.2
  • 320
    • 38049081662 scopus 로고    scopus 로고
    • Major depressive disorder
    • Belmaker RH, Agam G. Major depressive disorder. Engl J Med 2008; 358: 55-68.
    • (2008) Engl J Med , vol.358 , pp. 55-68
    • Belmaker, R.H.1    Agam, G.2
  • 321
    • 54049145992 scopus 로고    scopus 로고
    • Novel ketoenamine Schiffs bases from 7-hydroxy-4-methyl-2-oxo-2Hbenzo[h] chromene-8,10-dicarbaldehyde as potential antidyslipidemic and antioxidant agents
    • Sashidhara KV, Rosaiah JN, Bhatia G, Saxena JK. Novel ketoenamine Schiffs bases from 7-hydroxy-4-methyl-2-oxo-2Hbenzo[h] chromene-8,10-dicarbaldehyde as potential antidyslipidemic and antioxidant agents. Eur J Med Chem 2008; 43: 2592-6.
    • (2008) Eur J Med Chem , vol.43 , pp. 2592-2596
    • Sashidhara, K.V.1    Rosaiah, J.N.2    Bhatia, G.3    Saxena, J.K.4
  • 322
    • 77955280072 scopus 로고    scopus 로고
    • Antidepressant-like effect of scopoletin, a coumarin isolated from Polygala sabulosa (Polygalaceae) in mice: Evidence for the involvement of monoaminergic systems
    • Capra JC, Cunha MP, Machado DG, et al. Antidepressant-like effect of scopoletin, a coumarin isolated from Polygala sabulosa (Polygalaceae) in mice: evidence for the involvement of monoaminergic systems. Eur J Pharmacol 2010; 643: 232-8.
    • (2010) Eur J Pharmacol , vol.643 , pp. 232-238
    • Capra, J.C.1    Cunha, M.P.2    McHado, D.G.3
  • 323
    • 64249148289 scopus 로고    scopus 로고
    • Total synthesis of psoralidin, an anticancer natural product
    • Pahari P, Rohr J. Total synthesis of psoralidin, an anticancer natural product. J Org Chem 2009; 74: 2750-4.
    • (2009) J Org Chem , vol.74 , pp. 2750-2754
    • Pahari, P.1    Rohr, J.2
  • 324
    • 38849123655 scopus 로고    scopus 로고
    • Antidepressant-like effects of psoralidin isolated from the seeds of Psoralea corylifolia in the forced swimming test in mice
    • Yi LT, Li YC, Pan Y, et al. Antidepressant-like effects of psoralidin isolated from the seeds of Psoralea corylifolia in the forced swimming test in mice. Progr Neuropsychopharmacol Biol Psychiatr 2008; 32: 510-9.
    • (2008) Progr Neuropsychopharmacol Biol Psychiatr , vol.32 , pp. 510-519
    • Yi, L.T.1    Li, Y.C.2    Pan, Y.3
  • 325
    • 43049136833 scopus 로고    scopus 로고
    • Transcriptional regulation of corticotrophin releasing factor gene by furocoumarins isolated from seeds of Psoralea corylifolia
    • Chen YC, Cheung YT, Kong LD, et al. Transcriptional regulation of corticotrophin releasing factor gene by furocoumarins isolated from seeds of Psoralea corylifolia. Life Sci 2008; 82: 1117-21.
    • (2008) Life Sci , vol.82 , pp. 1117-1121
    • Chen, Y.C.1    Cheung, Y.T.2    Kong, L.D.3
  • 326
    • 79952484119 scopus 로고    scopus 로고
    • Discovery and synthesis of novel 3-phenylcoumarin derivatives as antidepressant agents
    • Sashidhara KV, Kumar A, Chatterjee M, et al. Discovery and synthesis of novel 3-phenylcoumarin derivatives as antidepressant agents. Bioorg Med Chem Lett 2011; 21: 1937-41.
    • (2011) Bioorg Med Chem Lett , vol.21 , pp. 1937-1941
    • Sashidhara, K.V.1    Kumar, A.2    Chatterjee, M.3
  • 327
    • 77952673774 scopus 로고    scopus 로고
    • Antidepressant-like profile and MAO-A inhibitory activity of 4-propyl-2H-benzo[h]-chromen-2-one
    • Vergel NE, López JL, Orallo F, et al. Antidepressant-like profile and MAO-A inhibitory activity of 4-propyl-2H-benzo[h]-chromen-2-one. Life Sci 2010; 86: 819-24.
    • (2010) Life Sci , vol.86 , pp. 819-824
    • Vergel, N.E.1    López, J.L.2    Orallo, F.3
  • 328
    • 43749087807 scopus 로고    scopus 로고
    • Synthesis and preliminary evaluation of some substituted coumarins as anticonvulsant agents
    • Amin KM, Rahman DEA, Al-Eryani YA. Synthesis and preliminary evaluation of some substituted coumarins as anticonvulsant agents. Bioorg Med Chem 2008; 16: 5377-88.
    • (2008) Bioorg Med Chem , vol.16 , pp. 5377-5388
    • Amin, K.M.1    Rahman, D.E.A.2    Al-Eryani, Y.A.3
  • 329
    • 70350136471 scopus 로고    scopus 로고
    • Advances in the research of piperazine compounds as receptor ligands
    • (in Chinese)
    • Gan LL, Cai JL, Zhou CH. Advances in the research of piperazine compounds as receptor ligands. Chin Pharma J 2009; 44: 1361-8 (in Chinese).
    • (2009) Chin Pharma J , vol.44 , pp. 1361-1368
    • Gan, L.L.1    Cai, J.L.2    Zhou, C.H.3
  • 330
    • 78650324940 scopus 로고    scopus 로고
    • Advances in the research of piperazine compounds as enzyme inhibitors
    • (in Chinese)
    • Gan LL, Lu YH, Zhou CH. Advances in the research of piperazine compounds as enzyme inhibitors. Chin J Biochem Pharm 2009; 30: 127-31 (in Chinese).
    • (2009) Chin J Biochem Pharm , vol.30 , pp. 127-131
    • Gan, L.L.1    Lu, Y.H.2    Zhou, C.H.3
  • 331
    • 70350501909 scopus 로고    scopus 로고
    • Recent advance in the research of piperazine-containing compounds as antimicrobial agents
    • (in Chinese)
    • Cai JL, Lu YH, Gan LL, Zhang YY, Zhou CH. Recent advance in the research of piperazine-containing compounds as antimicrobial agents. Chin J Antibiot 2009; 34: 454-62 (in Chinese).
    • (2009) Chin J Antibiot , vol.34 , pp. 454-462
    • Cai, J.L.1    Lu, Y.H.2    Gan, L.L.3    Zhang, Y.Y.4    Zhou, C.H.5
  • 332
    • 78650376370 scopus 로고    scopus 로고
    • Synthesis of azole-containing piperazine derivatives and evaluation of their antibacterial, antifungal and cytotoxic activities
    • Gan LL, Zhou CH. Synthesis of azole-containing piperazine derivatives and evaluation of their antibacterial, antifungal and cytotoxic activities. Bull Korean Chem Soc 2010; 31: 3684-92.
    • (2010) Bull Korean Chem Soc , vol.31 , pp. 3684-3692
    • Gan, L.L.1    Zhou, C.H.2
  • 333
    • 80455143393 scopus 로고    scopus 로고
    • Synthesis and their evaluation for their antimicrobial activity of diphenyl piperazine-based sulfanilamides
    • (in Chinese)
    • Wang XL, Gan LL, Yan CY, Zhou CH. Synthesis and their evaluation for their antimicrobial activity of diphenyl piperazine-based sulfanilamides. Scientia Sinica Chimica 2011; 41: 451-60 (in Chinese).
    • (2011) Scientia Sinica Chimica , vol.41 , pp. 451-460
    • Wang, X.L.1    Gan, L.L.2    Yan, C.Y.3    Zhou, C.H.4
  • 336
    • 77958067742 scopus 로고    scopus 로고
    • Synthesis and antihyperlipidemic activity of novel coumarin bisindole derivatives
    • Sashidhara KV, Kumar A, Kumar M, Srivastava A, Puri A. Synthesis and antihyperlipidemic activity of novel coumarin bisindole derivatives. Bioorg Med Chem Lett 2010; 20: 6504-7.
    • (2010) Bioorg Med Chem Lett , vol.20 , pp. 6504-6507
    • Sashidhara, K.V.1    Kumar, A.2    Kumar, M.3    Srivastava, A.4    Puri, A.5
  • 337
    • 0004260535 scopus 로고    scopus 로고
    • Definition and emergence of supramolecular chemistry
    • Steed JW, Atwood JL, Gale PA. Definition and emergence of supramolecular chemistry. Supramol Chem 2012; 1: 3-7.
    • (2012) Supramol Chem , vol.1 , pp. 3-7
    • Steed, J.W.1    Atwood, J.L.2    Gale, P.A.3
  • 338
  • 339
    • 70349544081 scopus 로고    scopus 로고
    • Antibacterial, spectral and thermal aspects of drug based-Cu(II) mixed ligand complexes
    • Kharadi GJ, Patel KD. Antibacterial, spectral and thermal aspects of drug based-Cu(II) mixed ligand complexes. Appl Organometal Chem 2009; 23: 391-7.
    • (2009) Appl Organometal Chem , vol.23 , pp. 391-397
    • Kharadi, G.J.1    Patel, K.D.2
  • 340
    • 77949683809 scopus 로고    scopus 로고
    • In-vitro antimicrobial, thermal and spectral studies of mixed ligand Cu(II) heterochelates of clioquinol and coumarin derivatives
    • Kharadi GJ, Patel KD. In-vitro antimicrobial, thermal and spectral studies of mixed ligand Cu(II) heterochelates of clioquinol and coumarin derivatives. Appl Organometal Chem 2010; 24: 332-7.
    • (2010) Appl Organometal Chem , vol.24 , pp. 332-337
    • Kharadi, G.J.1    Patel, K.D.2
  • 341
    • 37249082899 scopus 로고    scopus 로고
    • Catalytic epoxidation of olefins with hydrogen peroxide by hybrid complex containing nickel(III) Schiff base complex covalently linked to polyoxometalate
    • Mirkhani V, Moghadam M, Tangestaninejad S, Mohammadpoor-Baltork I, Shams E, Rasouli N. Catalytic epoxidation of olefins with hydrogen peroxide by hybrid complex containing nickel(III) Schiff base complex covalently linked to polyoxometalate. Appl Catal A 2008; 334: 106-11.
    • (2008) Appl Catal A , vol.334 , pp. 106-111
    • Mirkhani, V.1    Moghadam, M.2    Tangestaninejad, S.3    Mohammadpoor-Baltork, I.4    Shams, E.5    Rasouli, N.6
  • 342
    • 44649135119 scopus 로고    scopus 로고
    • Cr(III), Fe(III) and Co(III) complexes of tetradentate (ONNO) Schiff base ligands: Synthesis, characterization, properties and biological activity
    • Keskioglu E, Gunduzalp AB, Cete S, Hamurcu F, Erk B. Cr(III), Fe(III) and Co(III) complexes of tetradentate (ONNO) Schiff base ligands: synthesis, characterization, properties and biological activity. Spectrochim Acta 2008; 70A: 634-40.
    • (2008) Spectrochim Acta , vol.70 A , pp. 634-640
    • Keskioglu, E.1    Gunduzalp, A.B.2    Cete, S.3    Hamurcu, F.4    Erk, B.5
  • 343
    • 70349843256 scopus 로고    scopus 로고
    • Preparation and antimicrobial activity of s-triazine hydrazones of 7-hydroxy coumarin and their metal complexes
    • Jani GR, Vyas KB, Franco Z. Preparation and antimicrobial activity of s-triazine hydrazones of 7-hydroxy coumarin and their metal complexes. E-J Chem 2009; 6: 1228-32.
    • (2009) E-J Chem , vol.6 , pp. 1228-1232
    • Jani, G.R.1    Vyas, K.B.2    Franco, Z.3
  • 344
    • 77955492722 scopus 로고    scopus 로고
    • Novel inhibition of some pathogenic fungal and bacterial species by new synthetic phytochemical coumarin derivatives
    • Geweely NS. Novel inhibition of some pathogenic fungal and bacterial species by new synthetic phytochemical coumarin derivatives. Ann Microbiol 2009; 59: 359-68.
    • (2009) Ann Microbiol , vol.59 , pp. 359-368
    • Geweely, N.S.1
  • 345
    • 80052021303 scopus 로고    scopus 로고
    • Synthesis, characterization, antimicrobial, and DNA cleavage studies of metal complexes of coumarin Schiff bases
    • Phaniband MA, Dhumwad SD, Pattan SR. Synthesis, characterization, antimicrobial, and DNA cleavage studies of metal complexes of coumarin Schiff bases. Med Chem Res 2011; 20: 493-502.
    • (2011) Med Chem Res , vol.20 , pp. 493-502
    • Phaniband, M.A.1    Dhumwad, S.D.2    Pattan, S.R.3
  • 346
    • 84872486270 scopus 로고    scopus 로고
    • Synthesis, characterization, biological and thermal behaviour of Co(II), Ni(II) and Cu(II) complexes with Schiff bases having coumarin moieties
    • Patil SA, Unki SN, Badami PS. Synthesis, characterization, biological and thermal behaviour of Co(II), Ni(II) and Cu(II) complexes with Schiff bases having coumarin moieties. J Therm Anal Calorim 2013; 111: 1281-9.
    • (2013) J Therm Anal Calorim , vol.111 , pp. 1281-1289
    • Patil, S.A.1    Unki, S.N.2    Badami, P.S.3
  • 347
    • 84055211691 scopus 로고    scopus 로고
    • In vitro antibacterial, antifungal, and DNA cleavage studies of coumarin Schiff bases and their metal complexes: Synthesis and spectral characterization
    • Patil SA, Unki SN, Badami PS. In vitro antibacterial, antifungal, and DNA cleavage studies of coumarin Schiff bases and their metal complexes: synthesis and spectral characterization. Med Chem Res 2012; 21: 4017-27.
    • (2012) Med Chem Res , vol.21 , pp. 4017-4027
    • Patil, S.A.1    Unki, S.N.2    Badami, P.S.3
  • 348
    • 68949220072 scopus 로고    scopus 로고
    • Copper(II) complexes of coumarin-derived Schiff bases and their anti-Candida activity
    • Creaven BS, Devereux M, Karcz D, et al. Copper(II) complexes of coumarin-derived Schiff bases and their anti-Candida activity. J Inorg Biochem 2009; 103: 1196-203.
    • (2009) J Inorg Biochem , vol.103 , pp. 1196-1203
    • Creaven, B.S.1    Devereux, M.2    Karcz, D.3
  • 349
    • 80052927468 scopus 로고    scopus 로고
    • Novel transition metal complexes of 4-hydroxy-coumarin-3-thiocarbohydrazone: Pharmacodynamic of Co(III) on rats and antimicrobial activity
    • Mosaa AI, Emara AAA, Yousef JM, Saddiq AA. Novel transition metal complexes of 4-hydroxy-coumarin-3-thiocarbohydrazone: pharmacodynamic of Co(III) on rats and antimicrobial activity. Spectrochim Acta, Part A 2011; 81: 35-43.
    • (2011) Spectrochim Acta, Part A , vol.81 , pp. 35-43
    • Mosaa, A.I.1    Emara, A.A.A.2    Yousef, J.M.3    Saddiq, A.A.4
  • 350
    • 79960263867 scopus 로고    scopus 로고
    • Co(II), Ni(II) and Cu(II) complexes with coumarin-8-yl Schiff-bases: Spectroscopic, in vitro antimicrobial, DNA cleavage and uorescence studies
    • Patil SA, Unki SN, Kulkarni AD, Naik VH, Badami PS. Co(II), Ni(II) and Cu(II) complexes with coumarin-8-yl Schiff-bases: Spectroscopic, in vitro antimicrobial, DNA cleavage and uorescence studies. Spectrochim Acta 2011; 79A: 1128-36.
    • (2011) Spectrochim Acta , vol.79 A , pp. 1128-1136
    • Patil, S.A.1    Unki, S.N.2    Kulkarni, A.D.3    Naik, V.H.4    Badami, P.S.5
  • 351
    • 59749103154 scopus 로고    scopus 로고
    • Bivalent transition metal complexes of coumarin-3-yl thiosemicarbazone derivatives: Spectroscopic, antibacterial activity and thermogravimetric studies
    • Refat MS, El-Deen IM, Anwer ZM, El-Ghol S. Bivalent transition metal complexes of coumarin-3-yl thiosemicarbazone derivatives: spectroscopic, antibacterial activity and thermogravimetric studies. J Mol Struct 2009; 20: 149-62.
    • (2009) J Mol Struct , vol.20 , pp. 149-162
    • Refat, M.S.1    El-Deen, I.M.2    Anwer, Z.M.3    El-Ghol, S.4
  • 352
    • 72649095416 scopus 로고    scopus 로고
    • DNA cleavage, antimicrobial, spectroscopic and uorescence studies of Co(II), Ni(II) and Cu(II) complexes with SNO donor coumarin Schiff bases
    • Patil SA, Naik VH, Kulkarni AD, Badami PS. DNA cleavage, antimicrobial, spectroscopic and uorescence studies of Co(II), Ni(II) and Cu(II) complexes with SNO donor coumarin Schiff bases. Spectrochim Acta 2010; 75A: 347-54.
    • (2010) Spectrochim Acta , vol.75 A , pp. 347-354
    • Patil, S.A.1    Naik, V.H.2    Kulkarni, A.D.3    Badami, P.S.4
  • 353
    • 56949104357 scopus 로고    scopus 로고
    • Synthesis, spectral characterization, in vitro antibacterial, antifungal and cytotoxic activities of Co(II), Ni(II) and Cu(II) complexes with 1,2,4-triazole Schiff bases
    • Bagihalli GB, Avaji PG, Patil SA, Badami PS. Synthesis, spectral characterization, in vitro antibacterial, antifungal and cytotoxic activities of Co(II), Ni(II) and Cu(II) complexes with 1,2,4-triazole Schiff bases. Eur J Med Chem 2008; 43: 2639-49.
    • (2008) Eur J Med Chem , vol.43 , pp. 2639-2649
    • Bagihalli, G.B.1    Avaji, P.G.2    Patil, S.A.3    Badami, P.S.4
  • 354
    • 78650680130 scopus 로고    scopus 로고
    • Synthesis, characterization, in vitro antimicrobial and DNA cleavage studies of Co(II), Ni(II) and Cu(II) complexes with ONOO donor coumarin Schiff bases
    • Patil SA, Unki SN, Kulkarni AD, Naik VH, Badami PS. Synthesis, characterization, in vitro antimicrobial and DNA cleavage studies of Co(II), Ni(II) and Cu(II) complexes with ONOO donor coumarin Schiff bases. J Mol Struct 2011; 985: 330-8.
    • (2011) J Mol Struct , vol.985 , pp. 330-338
    • Patil, S.A.1    Unki, S.N.2    Kulkarni, A.D.3    Naik, V.H.4    Badami, P.S.5
  • 355
    • 80054045366 scopus 로고    scopus 로고
    • Microwave assisted synthesis, spectroscopic, electrochemical and DNA cleavage studies of Lanthanide(III) complexes with coumarin based imines
    • Kapoor P, Fahmi N, Singh RV. Microwave assisted synthesis, spectroscopic, electrochemical and DNA cleavage studies of Lanthanide(III) complexes with coumarin based imines. Spectrochim Acta 2011; 83A: 74-81.
    • (2011) Spectrochim Acta , vol.83 A , pp. 74-81
    • Kapoor, P.1    Fahmi, N.2    Singh, R.V.3
  • 356
    • 67349208473 scopus 로고    scopus 로고
    • Synthesis, characterization, DNA cleavage and in vitro antimicrobial studies of La(III), Th(IV) and VO(IV) complexes with Schiff bases of coumarin derivatives
    • Kulkarni A, Patil SA, Badami PS. Synthesis, characterization, DNA cleavage and in vitro antimicrobial studies of La(III), Th(IV) and VO(IV) complexes with Schiff bases of coumarin derivatives. Eur J Med Chem 2009; 44: 2904-12.
    • (2009) Eur J Med Chem , vol.44 , pp. 2904-2912
    • Kulkarni, A.1    Patil, S.A.2    Badami, P.S.3
  • 357
    • 79952576889 scopus 로고    scopus 로고
    • Structure, photophysics, electrochemistry, DFT calculation, and in-vitro antioxidant activity of coumarin Schiff base complexes of group 6 metal carbonyls
    • Datta P, Mukhopadhyay AP, Manna P, Tiekink ERT, Sil PC, Sinha C. Structure, photophysics, electrochemistry, DFT calculation, and in-vitro antioxidant activity of coumarin Schiff base complexes of group 6 metal carbonyls. J Inorg Biochem 2011; 105: 577-88.
    • (2011) J Inorg Biochem , vol.105 , pp. 577-588
    • Datta, P.1    Mukhopadhyay, A.P.2    Manna, P.3    Tiekink, E.R.T.4    Sil, P.C.5    Sinha, C.6
  • 358
    • 79960283033 scopus 로고    scopus 로고
    • Antitubercular and fluorescence studies of copper(II) complexes with quinolone family member, ciprofloxacin
    • Kharadi GJ. Antitubercular and fluorescence studies of copper(II) complexes with quinolone family member, ciprofloxacin. Spectrochim Acta 2011; 79A: 898-903.
    • (2011) Spectrochim Acta , vol.79 A , pp. 898-903
    • Kharadi, G.J.1
  • 359
    • 68349089227 scopus 로고    scopus 로고
    • Synthesis, spectroscopic, thermal and biological aspect of mixed ligand copper(II) complexes
    • Kharadi GJ, Patel KD. Synthesis, spectroscopic, thermal and biological aspect of mixed ligand copper(II) complexes. J Therm Anal Calorim 2009; 96: 1019-28.
    • (2009) J Therm Anal Calorim , vol.96 , pp. 1019-1028
    • Kharadi, G.J.1    Patel, K.D.2
  • 360
    • 84865429257 scopus 로고    scopus 로고
    • Multiple heating rate kinetic parameters, thermal, X-ray diffraction studies of newly synthesized octahedral copper complexes based on bromo-coumarins along with their antioxidant, anti-tubercular and antimicrobial activity evaluation
    • Patel KS, Patel JC, Dholariya HR, Patel KD. Multiple heating rate kinetic parameters, thermal, X-ray diffraction studies of newly synthesized octahedral copper complexes based on bromo-coumarins along with their antioxidant, anti-tubercular and antimicrobial activity evaluation. Spectrochim Acta 2012; 96A: 468-79.
    • (2012) Spectrochim Acta , vol.96 A , pp. 468-479
    • Patel, K.S.1    Patel, J.C.2    Dholariya, H.R.3    Patel, K.D.4
  • 361
    • 54049099600 scopus 로고    scopus 로고
    • Synthesis, characterization of copper(II), cobalt(II), nickel(II), zinc(II) and cadmium(II) complexes of [7-hydroxy-4-methyl-8-coumarinyl]glycine and a comparitive study of their microbial activities
    • Gudasi KB, Patil MS, Vadavi RS. Synthesis, characterization of copper(II), cobalt(II), nickel(II), zinc(II) and cadmium(II) complexes of [7-hydroxy-4-methyl-8-coumarinyl]glycine and a comparitive study of their microbial activities. Eur J Med Chem 2008; 43: 2436-41.
    • (2008) Eur J Med Chem , vol.43 , pp. 2436-2441
    • Gudasi, K.B.1    Patil, M.S.2    Vadavi, R.S.3
  • 362
    • 34548399452 scopus 로고    scopus 로고
    • Metallophrobes: Synthesis, characterisation, and potency of a novel gallium(III) complex in human epidermal carcinoma cells
    • Harpstrite SE, Prior JL, Rath NP, Sharma V. Metallophrobes: synthesis, characterisation, and potency of a novel gallium(III) complex in human epidermal carcinoma cells. J Inorg Biochem 2007; 101: 1347-53.
    • (2007) J Inorg Biochem , vol.101 , pp. 1347-1353
    • Harpstrite, S.E.1    Prior, J.L.2    Rath, N.P.3    Sharma, V.4
  • 363
    • 78149455065 scopus 로고    scopus 로고
    • Biological activity and coordination modes of copper(II) complexes of Schiff base-derived coumarin ligands
    • Creaven BS, Czeglédi E, Devereux M, et al. Biological activity and coordination modes of copper(II) complexes of Schiff base-derived coumarin ligands. Dalton Trans 2010; 39: 10854-65.
    • (2010) Dalton Trans , vol.39 , pp. 10854-10865
    • Creaven, B.S.1    Czeglédi, E.2    Devereux, M.3
  • 364
    • 58149168727 scopus 로고    scopus 로고
    • Role of cell cycle events and apoptosis in mediating the anti-cancer activity of a silver(I) complex of 4-hydroxy-3-nitro-coumarin-bis(phenanthroline) in human malignant cancer cells
    • Thati B, Noble A, Creaven BS, et al. Role of cell cycle events and apoptosis in mediating the anti-cancer activity of a silver(I) complex of 4-hydroxy-3-nitro-coumarin-bis(phenanthroline) in human malignant cancer cells. Eur J Pharmacol 2009; 602: 203-14.
    • (2009) Eur J Pharmacol , vol.602 , pp. 203-214
    • Thati, B.1    Noble, A.2    Creaven, B.S.3
  • 365
    • 79551718490 scopus 로고    scopus 로고
    • Lanthanide complexes with LL-diketones and coumarin derivates: Synthesis, thermal behaviour, optical and pharmacological properties and immobilization
    • Milanova M, Zaharieva J, Manolov I, Getzova M, Todorovsky D. Lanthanide complexes with LL-diketones and coumarin derivates: synthesis, thermal behaviour, optical and pharmacological properties and immobilization. J Rare Earths 2010; 28: 66-74.
    • (2010) J Rare Earths , vol.28 , pp. 66-74
    • Milanova, M.1    Zaharieva, J.2    Manolov, I.3    Getzova, M.4    Todorovsky, D.5
  • 366
    • 80053110441 scopus 로고    scopus 로고
    • Diagnostic agents-types and applications: A discussion
    • Misra SK, Varma A, Mishra AK. Diagnostic agents-types and applications: a discussion. Rasayan J Chem 2011; 4: 492-7.
    • (2011) Rasayan J Chem , vol.4 , pp. 492-497
    • Misra, S.K.1    Varma, A.2    Mishra, A.K.3
  • 368
    • 55949111485 scopus 로고    scopus 로고
    • Fluorescent single-stranded DNA binding protein as a probe for sensitive, real-time assays of helicase activity
    • Dillingham MS, Tibbles KL, Hunter JL, Bell JC, Kowalczykowski SC, Webb MR. Fluorescent single-stranded DNA binding protein as a probe for sensitive, real-time assays of helicase activity. Biophys J 2008; 95: 3330-9.
    • (2008) Biophys J , vol.95 , pp. 3330-3339
    • Dillingham, M.S.1    Tibbles, K.L.2    Hunter, J.L.3    Bell, J.C.4    Kowalczykowski, S.C.5    Webb, M.R.6
  • 370
    • 84862085568 scopus 로고    scopus 로고
    • Heteroditopic receptors for ion-pair recognition
    • McConnell AJ, Beer PD. Heteroditopic receptors for ion-pair recognition. Angew Chem Int Ed 2012; 51: 5052-61.
    • (2012) Angew Chem Int Ed , vol.51 , pp. 5052-5061
    • McConnell, A.J.1    Beer, P.D.2
  • 371
    • 79960964939 scopus 로고    scopus 로고
    • Imidazole-bearing tetraphenylethylene: Uorescent probe for metal ions based on AIE feature
    • Bian N, Chen Q, Qiu XL, Qi AD, Han BH. Imidazole-bearing tetraphenylethylene: uorescent probe for metal ions based on AIE feature. New J Chem 2011; 35: 1667-71.
    • (2011) New J Chem , vol.35 , pp. 1667-1671
    • Bian, N.1    Chen, Q.2    Qiu, X.L.3    Qi, A.D.4    Han, B.H.5
  • 372
    • 63049095171 scopus 로고    scopus 로고
    • (Thio)urea organocatalysis-What can be learnt from anion recognition?
    • Zhang ZG, Schreiner PR. (Thio)urea organocatalysis-What can be learnt from anion recognition? Chem Soc Rev 2009; 38: 1187-98.
    • (2009) Chem Soc Rev , vol.38 , pp. 1187-1198
    • Zhang, Z.G.1    Schreiner, P.R.2
  • 373
    • 80455137108 scopus 로고    scopus 로고
    • Recent advances in researches of triazole-based supramolecular chemistry and medicinal drugs
    • (in Chinese)
    • Chang JJ, Wang Y, Zhang HZ, Zhou CH, Geng RX, Ji QG. Recent advances in researches of triazole-based supramolecular chemistry and medicinal drugs. Chem J Chin Univ 2011; 32: 1970-85 (in Chinese).
    • (2011) Chem J Chin Univ , vol.32 , pp. 1970-1985
    • Chang, J.J.1    Wang, Y.2    Zhang, H.Z.3    Zhou, C.H.4    Geng, R.X.5    Ji, Q.G.6
  • 374
    • 77954899257 scopus 로고    scopus 로고
    • Combining supramolecular chemistry with biology
    • Uhlenheuer DA, Petkau K, Brunsveld L. Combining supramolecular chemistry with biology. Chem Soc Rev 2010; 39: 2817-26.
    • (2010) Chem Soc Rev , vol.39 , pp. 2817-2826
    • Uhlenheuer, D.A.1    Petkau, K.2    Brunsveld, L.3
  • 375
    • 44849102395 scopus 로고    scopus 로고
    • Metals in neurobiology: Probing their chemistry and biology with molecular imaging
    • Que EL, Domaille DW, Chang CJ. Metals in neurobiology: probing their chemistry and biology with molecular imaging. Chem Rev 2008; 108: 1517-49.
    • (2008) Chem Rev , vol.108 , pp. 1517-1549
    • Que, E.L.1    Domaille, D.W.2    Chang, C.J.3
  • 378
    • 67749114482 scopus 로고    scopus 로고
    • 2+-selective fluorescence sensor: Synthesis, mechanisms, and applications in living cells
    • 2+-selective fluorescence sensor: synthesis, mechanisms, and applications in living cells. J Am Chem Soc 2009; 131: 2008-12.
    • (2009) J Am Chem Soc , vol.131 , pp. 2008-2012
    • Jung, H.S.1    Kwon, P.S.2    Lee, J.W.3
  • 380
    • 84862909311 scopus 로고    scopus 로고
    • 2+chemodosimeters and the applications for living cell imaging
    • 2+chemodosimeters and the applications for living cell imaging. Org Lett 2012; 14: 432-5.
    • (2012) Org Lett , vol.14 , pp. 432-435
    • Yuan, L.1    Lin, W.Y.2    Chen, B.3    Xie, Y.N.4
  • 381
    • 52449129296 scopus 로고    scopus 로고
    • Fluorescence imaging of intracellular cadmium using a dual-excitation ratiometric chemosensor
    • Taki M, Desaki M, Ojida A, et al. Fluorescence imaging of intracellular cadmium using a dual-excitation ratiometric chemosensor. J Am Chem Soc 2008; 130: 12564-5.
    • (2008) J Am Chem Soc , vol.130 , pp. 12564-12565
    • Taki, M.1    Desaki, M.2    Ojida, A.3
  • 382
    • 58649119813 scopus 로고    scopus 로고
    • Anion receptors that contain metals as structural units
    • Amendola V, Fabbrizzi L. Anion receptors that contain metals as structural units. Chem Commun 2009; 513-31.
    • (2009) Chem Commun , pp. 513-531
    • Amendola, V.1    Fabbrizzi, L.2
  • 383
    • 77957167823 scopus 로고    scopus 로고
    • Rational design of FRET-based ratiometric chemosensors for in vitro and in cell fluorescence analyses of nucleoside polyphosphates
    • Kurishita Y, Kohira T, Ojida A, Hamachi I. Rational design of FRET-based ratiometric chemosensors for in vitro and in cell fluorescence analyses of nucleoside polyphosphates. J Am Chem Soc 2010; 132: 13290-9.
    • (2010) J Am Chem Soc , vol.132 , pp. 13290-13299
    • Kurishita, Y.1    Kohira, T.2    Ojida, A.3    Hamachi, I.4
  • 384
    • 79952578095 scopus 로고    scopus 로고
    • Visualization of nitroxyl in living cells by a chelated copper(II) coumarin complex
    • Zhou Y, Liu K, Li JY, Fang Y, Zhao TC, Yao C. Visualization of nitroxyl in living cells by a chelated copper(II) coumarin complex. Org Lett 2011; 13: 1290-3.
    • (2011) Org Lett , vol.13 , pp. 1290-1293
    • Zhou, Y.1    Liu, K.2    Li, J.Y.3    Fang, Y.4    Zhao, T.C.5    Yao, C.6
  • 385
    • 80455164883 scopus 로고    scopus 로고
    • Ethidium bromide fluorescence probe on the interaction between dinuclear macrocyclic polyamine Zn(II) complex and DNA
    • (in Chinese)
    • Li S, Zhou CH, Chen JX, Xiang QX. Ethidium bromide fluorescence probe on the interaction between dinuclear macrocyclic polyamine Zn(II) complex and DNA. Chin J Appl Chem 2009; 26: 1461-5 (in Chinese).
    • (2009) Chin J Appl Chem , vol.26 , pp. 1461-1465
    • Li, S.1    Zhou, C.H.2    Chen, J.X.3    Xiang, Q.X.4
  • 386
    • 79954480112 scopus 로고    scopus 로고
    • New generation of amino coumarin methyl sulfonate-based fluorogenic substrates for amidase assays in droplet-based microfluidic applications
    • Worono G, El Harrak A, Mayot E, et al. New generation of amino coumarin methyl sulfonate-based fluorogenic substrates for amidase assays in droplet-based microfluidic applications. Anal Chem 2011; 83: 2852-7.
    • (2011) Anal Chem , vol.83 , pp. 2852-2857
    • Worono, G.1    El Harrak, A.2    Mayot, E.3
  • 387
    • 77951682590 scopus 로고    scopus 로고
    • Suborganelle sensing of mitochondrial cAMP-dependent protein kinase activity
    • Agnes RS, Jernigan F, Shell JR, Sharma V, Lawrence DS. Suborganelle sensing of mitochondrial cAMP-dependent protein kinase activity. J Am Chem Soc 2010; 132: 6075-80.
    • (2010) J Am Chem Soc , vol.132 , pp. 6075-6080
    • Agnes, R.S.1    Jernigan, F.2    Shell, J.R.3    Sharma, V.4    Lawrence, D.S.5
  • 388
    • 56349110884 scopus 로고    scopus 로고
    • Control of mitochondria dynamics and oxidative metabolism by cAMP, AKAPs and the proteasome
    • Carlucci A, Lignitto L, Feliciello A. Control of mitochondria dynamics and oxidative metabolism by cAMP, AKAPs and the proteasome. Trends Cell Biol 2008; 18: 604-13.
    • (2008) Trends Cell Biol , vol.18 , pp. 604-613
    • Carlucci, A.1    Lignitto, L.2    Feliciello, A.3
  • 389
    • 67649458218 scopus 로고    scopus 로고
    • Anion sensorbased ratiometric peptide probe for protein kinase activity
    • Kikuchi K, Hashimoto S, Mizukami S, Nagano T. Anion sensorbased ratiometric peptide probe for protein kinase activity. Org Lett 2009; 11: 2732-5.
    • (2009) Org Lett , vol.11 , pp. 2732-2735
    • Kikuchi, K.1    Hashimoto, S.2    Mizukami, S.3    Nagano, T.4
  • 390
    • 79951640929 scopus 로고    scopus 로고
    • Simultaneous intracellular β-D-glucosidase and phosphodiesterase I activities measurements based on a triple-signaling fluorescent probe
    • Li YH, Wang H, Li J, Zheng J, Xu XH, Yang RH. Simultaneous intracellular β-D-glucosidase and phosphodiesterase I activities measurements based on a triple-signaling fluorescent probe. Anal Chem 2011; 83: 1268-74.
    • (2011) Anal Chem , vol.83 , pp. 1268-1274
    • Li, Y.H.1    Wang, H.2    Li, J.3    Zheng, J.4    Xu, X.H.5    Yang, R.H.6
  • 392
    • 77956252905 scopus 로고    scopus 로고
    • Design and synthesis of a long-wavelength latent fluorogenic substrate for salicylate hydroxylase: A useful fluorimetric indicator for analyte determination by dehydrogenase-coupled biosensors
    • Huang ST, Teng CJ, Lee YH, Wu JY, Wang KL, Lin CM. Design and synthesis of a long-wavelength latent fluorogenic substrate for salicylate hydroxylase: a useful fluorimetric indicator for analyte determination by dehydrogenase-coupled biosensors. Anal Chem 2010; 82: 7329-34.
    • (2010) Anal Chem , vol.82 , pp. 7329-7334
    • Huang, S.T.1    Teng, C.J.2    Lee, Y.H.3    Wu, J.Y.4    Wang, K.L.5    Lin, C.M.6
  • 393
    • 84857653924 scopus 로고    scopus 로고
    • Evaluation of fluorescent phosphatidylserine substrates for the aminophospholipid flippase in mammalian cells
    • Smith BA, O'Neil EJ, Lampkins AJ, et al. Evaluation of fluorescent phosphatidylserine substrates for the aminophospholipid flippase in mammalian cells. J Fluoresc 2012; 22: 93-101.
    • (2012) J Fluoresc , vol.22 , pp. 93-101
    • Smith, B.A.1    O'Neil, E.J.2    Lampkins, A.J.3
  • 394
    • 70349731740 scopus 로고    scopus 로고
    • Reconstitution of phospholipids translocase activity with purified Drs2p, a type-IV P-type ATPase from budding yeast
    • Zhou XM, Graham TR. Reconstitution of phospholipids translocase activity with purified Drs2p, a type-IV P-type ATPase from budding yeast. Proc Natl Acad Sci USA 2009; 106: 16586-91.
    • (2009) Proc Natl Acad Sci USA , vol.106 , pp. 16586-16591
    • Zhou, X.M.1    Graham, T.R.2
  • 395
    • 70450242726 scopus 로고    scopus 로고
    • Localization, purification, and functional reconstitution of the P4-ATPase Atp8a2, a phosphatidylserine flippase in photoreceptor disc membranes
    • Coleman JA, Kwok MCM, Molday RS. Localization, purification, and functional reconstitution of the P4-ATPase Atp8a2, a phosphatidylserine flippase in photoreceptor disc membranes. J Biol Chem 2009; 284: 32670-9.
    • (2009) J Biol Chem , vol.284 , pp. 32670-32679
    • Coleman, J.A.1    Kwok, M.C.M.2    Molday, R.S.3
  • 397
    • 84862901653 scopus 로고    scopus 로고
    • An activity-based fluorogenic probe for sensitive and selective monoamine oxidase-B detection
    • Long SB, Chen L, Xiang YM, Song MG, Zheng YG, Zhu Q. An activity-based fluorogenic probe for sensitive and selective monoamine oxidase-B detection. Chem Commun 2012; 48: 7164-6.
    • (2012) Chem Commun , vol.48 , pp. 7164-7166
    • Long, S.B.1    Chen, L.2    Xiang, Y.M.3    Song, M.G.4    Zheng, Y.G.5    Zhu, Q.6
  • 398
    • 38049057786 scopus 로고    scopus 로고
    • Selective activity-based probes for cysteine cathepsins
    • Watzke A, Kosec G, Kindermann M, et al. Selective activity-based probes for cysteine cathepsins. Angew Chem Int Ed 2008; 47: 406-9.
    • (2008) Angew Chem Int Ed , vol.47 , pp. 406-409
    • Watzke, A.1    Kosec, G.2    Kindermann, M.3
  • 399
    • 58849146539 scopus 로고    scopus 로고
    • Protease responsive nanoprobes with tethered fluorogenic peptidyl 3-arylcoumarin substrates
    • Welser K, Grilj J, Vauthey E, Aylott JW, Chan WC. Protease responsive nanoprobes with tethered fluorogenic peptidyl 3-arylcoumarin substrates. Chem Commun 2009; 671-3.
    • (2009) Chem Commun , pp. 671-673
    • Welser, K.1    Grilj, J.2    Vauthey, E.3    Aylott, J.W.4    Chan, W.C.5
  • 400
    • 77952824313 scopus 로고    scopus 로고
    • Fluorescent and colorimetric probes for detection of thiols
    • Chen XQ, Zhou Y, Peng XJ, Yoon J. Fluorescent and colorimetric probes for detection of thiols. Chem Soc Rev 2010; 39: 2120-35.
    • (2010) Chem Soc Rev , vol.39 , pp. 2120-2135
    • Chen, X.Q.1    Zhou, Y.2    Peng, X.J.3    Yoon, J.4
  • 401
    • 79951906200 scopus 로고    scopus 로고
    • Thiol-based redox switches and gene regulation
    • Antelmann H, Helmann JD. Thiol-based redox switches and gene regulation. Antioxid Redox Signal 2010; 14: 1049-63.
    • (2010) Antioxid Redox Signal , vol.14 , pp. 1049-1063
    • Antelmann, H.1    Helmann, J.D.2
  • 402
    • 75749123115 scopus 로고    scopus 로고
    • Orchestrating redox signaling networks through regulatory cysteine switches
    • Paulsen CE, Carroll KS. Orchestrating redox signaling networks through regulatory cysteine switches. ACS Chem Biol 2009; 5: 47-62.
    • (2009) ACS Chem Biol , vol.5 , pp. 47-62
    • Paulsen, C.E.1    Carroll, K.S.2
  • 403
    • 77950240233 scopus 로고    scopus 로고
    • Plasma homocysteine and cysteine and risk of breast cancer in women
    • Lin J, Lee IM, Song YQ, et al. Plasma homocysteine and cysteine and risk of breast cancer in women. Cancer Res 2010; 70: 2397-405.
    • (2010) Cancer Res , vol.70 , pp. 2397-2405
    • Lin, J.1    Lee, I.M.2    Song, Y.Q.3
  • 404
    • 77957592789 scopus 로고    scopus 로고
    • Regulation of survival, proliferation, invasion, angiogenesis, and metastasis of tumor cells through modulation of inflammatory pathways by nutraceuticals
    • Gupta SC, Kim JH, Prasad S, Aggarwal BB. Regulation of survival, proliferation, invasion, angiogenesis, and metastasis of tumor cells through modulation of inflammatory pathways by nutraceuticals. Cancer Metastasis Rev 2010; 29: 405-34.
    • (2010) Cancer Metastasis Rev , vol.29 , pp. 405-434
    • Gupta, S.C.1    Kim, J.H.2    Prasad, S.3    Aggarwal, B.B.4
  • 405
    • 84878658977 scopus 로고    scopus 로고
    • Oxidative stress and cardiovascular disease in diabetes mellitus
    • In Sauer H, Shah AM, Laurindo FRM. Eds, Humana Press: New York
    • Gupta D, Griendling KK, Taylor RW. Oxidative stress and cardiovascular disease in diabetes mellitus. In Sauer H, Shah AM, Laurindo FRM. Eds. Studies on cardiovascular disorders. Humana Press: New York 2010; pp. 263-79.
    • (2010) Studies on cardiovascular disorders , pp. 263-279
    • Gupta, D.1    Griendling, K.K.2    Taylor, R.W.3
  • 406
    • 75149165994 scopus 로고    scopus 로고
    • Update on the oxidative stress theory of aging: Does oxidative stress play a role in aging or healthy aging?
    • Salmon AB, Richardson A, Pérez VI. Update on the oxidative stress theory of aging: does oxidative stress play a role in aging or healthy aging? Free Radic Biol Med 2010; 48: 642-55.
    • (2010) Free Radic Biol Med , vol.48 , pp. 642-655
    • Salmon, A.B.1    Richardson, A.2    Pérez, V.I.3
  • 407
    • 79959397978 scopus 로고    scopus 로고
    • Colorimetric and fluorescent dual probe based on a polythiophene derivative for the detection of cysteine and homocysteine
    • Yao ZY, Bai H, Li C, Shi GQ. Colorimetric and fluorescent dual probe based on a polythiophene derivative for the detection of cysteine and homocysteine. Chem Commun 2011; 47: 7431-3.
    • (2011) Chem Commun , vol.47 , pp. 7431-7433
    • Yao, Z.Y.1    Bai, H.2    Li, C.3    Shi, G.Q.4
  • 408
    • 79952592188 scopus 로고    scopus 로고
    • Coumarin-based thiol chemosensor: Synthesis, turn-on mechanism, and its biological application
    • Jung HS, Ko KC, Kim GH, et al. Coumarin-based thiol chemosensor: synthesis, turn-on mechanism, and its biological application. Org Lett 2011; 13: 1498-501.
    • (2011) Org Lett , vol.13 , pp. 1498-1501
    • Jung, H.S.1    Ko, K.C.2    Kim, G.H.3
  • 409
    • 54349097780 scopus 로고    scopus 로고
    • Design of gold nanoparticle-based colorimetric biosensing assays
    • Zhao WA, Brook MA, Li YF. Design of gold nanoparticle-based colorimetric biosensing assays. ChemBioChem 2008; 9; 2363-71.
    • (2008) ChemBioChem , vol.9 , pp. 2363-2371
    • Zhao, W.A.1    Brook, M.A.2    Li, Y.F.3
  • 410
    • 84864705882 scopus 로고    scopus 로고
    • A cysteine probe with high selectivity and sensitivity promoted by response-assisted electrostatic attraction
    • Zhou X, Jin XJ, Sun GY, Li DH, Wu X. A cysteine probe with high selectivity and sensitivity promoted by response-assisted electrostatic attraction. Chem Commun 2012; 48: 8793-5.
    • (2012) Chem Commun , vol.48 , pp. 8793-8795
    • Zhou, X.1    Jin, X.J.2    Sun, G.Y.3    Li, D.H.4    Wu, X.5
  • 411
    • 79957789792 scopus 로고    scopus 로고
    • Ratiometric fluorescence imaging of cellular glutathione
    • Kim GJ, Lee K, Kwon H, Kim HJ. Ratiometric fluorescence imaging of cellular glutathione. Org Lett 2011; 13: 2799-801.
    • (2011) Org Lett , vol.13 , pp. 2799-2801
    • Kim, G.J.1    Lee, K.2    Kwon, H.3    Kim, H.J.4
  • 412
    • 56849126506 scopus 로고    scopus 로고
    • Fluorescence turn-on probe for homocysteine and cysteine in water
    • Lee KS, Kim TK, Lee JH, Kim HJ, Hong JI. Fluorescence turn-on probe for homocysteine and cysteine in water. Chem Commun 2008; 6173-5.
    • (2008) Chem Commun , pp. 6173-6175
    • Lee, K.S.1    Kim, T.K.2    Lee, J.H.3    Kim, H.J.4    Hong, J.I.5
  • 413
    • 80053306641 scopus 로고    scopus 로고
    • Nitroolefln-based coumarin as a colorimetric and fluorescent dual probe for biothiols
    • Sun YQ, Chen ML, Liu J, Lv X, Li JF, Guo W. Nitroolefln-based coumarin as a colorimetric and fluorescent dual probe for biothiols. Chem Commun 2011; 47: 11029-31.
    • (2011) Chem Commun , vol.47 , pp. 11029-11031
    • Sun, Y.Q.1    Chen, M.L.2    Liu, J.3    Lv, X.4    Li, J.F.5    Guo, W.6
  • 415
    • 80555122790 scopus 로고    scopus 로고
    • The development of a fluorescence turn-on sensor for cysteine, glutathione and other biothiols. A kinetic study
    • García-Beltrán O, Mena N, Pérez EG, et al. The development of a fluorescence turn-on sensor for cysteine, glutathione and other biothiols. A kinetic study. Tetrahedron Lett 2011; 52: 6606-9.
    • (2011) Tetrahedron Lett , vol.52 , pp. 6606-6609
    • García-Beltrán, O.1    Mena, N.2    Pérez, E.G.3
  • 416
    • 77958511070 scopus 로고    scopus 로고
    • Ratiometric fluorescent detection of intracellular hydroxyl radicals based on a hybrid coumarin-cyanine platform
    • Yuan L, Lin WY, Song JZ. Ratiometric fluorescent detection of intracellular hydroxyl radicals based on a hybrid coumarin-cyanine platform. Chem Commun 2010; 46: 7930-2.
    • (2010) Chem Commun , vol.46 , pp. 7930-7932
    • Yuan, L.1    Lin, W.Y.2    Song, J.Z.3
  • 417
    • 84860320854 scopus 로고    scopus 로고
    • A TEMPO-conjugated fluorescent probe for monitoring mitochondrial redox reactions
    • Hirosawa S, Arai S, Takeoka S. A TEMPO-conjugated fluorescent probe for monitoring mitochondrial redox reactions. Chem Commun 2012; 48: 4845-7.
    • (2012) Chem Commun , vol.48 , pp. 4845-4847
    • Hirosawa, S.1    Arai, S.2    Takeoka, S.3
  • 419
    • 80051797970 scopus 로고    scopus 로고
    • A novel fluorescent probe for more effective monitoring of nanosized drug delivery systems within the cells
    • Plajnšek KT, Pajk S, Govedarica B, Pečar S, Srčič S, Kristl J. A novel fluorescent probe for more effective monitoring of nanosized drug delivery systems within the cells. Int J Pharm 2011; 416: 384-93.
    • (2011) Int J Pharm , vol.416 , pp. 384-393
    • Plajnšek, K.T.1    Pajk, S.2    Govedarica, B.3    Pečar, S.4    Srčič, S.5    Kristl, J.6
  • 420
    • 79751523412 scopus 로고    scopus 로고
    • Construction of a thiamin sensor from the periplasmic thiamin binding protein
    • Hanes JW, Chatterjee D, Soriano EV, Ealick SE, Begley TP. Construction of a thiamin sensor from the periplasmic thiamin binding protein. Chem Commun 2011; 47: 2273-5.
    • (2011) Chem Commun , vol.47 , pp. 2273-2275
    • Hanes, J.W.1    Chatterjee, D.2    Soriano, E.V.3    Ealick, S.E.4    Begley, T.P.5
  • 421
    • 77953072474 scopus 로고    scopus 로고
    • Polyamines: Fundamental characters in chemistry and biology
    • Agostinelli E, Marques MPM, Calheiros R, et al. Polyamines: fundamental characters in chemistry and biology. Amino Acids 2010; 38: 393-403.
    • (2010) Amino Acids , vol.38 , pp. 393-403
    • Agostinelli, E.1    Marques, M.P.M.2    Calheiros, R.3
  • 422
    • 80051771404 scopus 로고    scopus 로고
    • A molecular probe for the optical detection of biogenic amines
    • Lee B, Scopelliti R, Severin K. A molecular probe for the optical detection of biogenic amines. Chem Commun 2011; 47: 9639-41.
    • (2011) Chem Commun , vol.47 , pp. 9639-9641
    • Lee, B.1    Scopelliti, R.2    Severin, K.3
  • 423
    • 70349276683 scopus 로고    scopus 로고
    • 2-Quinolone and coumarin polymethines for the detection of proteins using fluorescence
    • Kovalska VB, Volkova KD, Manaev AV, et al. 2-Quinolone and coumarin polymethines for the detection of proteins using fluorescence. Dyes Pigments 2010; 84: 159-64.
    • (2010) Dyes Pigments , vol.84 , pp. 159-164
    • Kovalska, V.B.1    Volkova, K.D.2    Manaev, A.V.3
  • 424
    • 70849105921 scopus 로고    scopus 로고
    • Staining of macromolecules: Possible mechanisms and examples
    • Prentoe P. Staining of macromolecules: possible mechanisms and examples. Biotech Histochem 2009; 84: 139-58.
    • (2009) Biotech Histochem , vol.84 , pp. 139-158
    • Prentoe, P.1
  • 425
    • 84877584561 scopus 로고    scopus 로고
    • Recent advances in application researches of thiazole compounds
    • (in Chinese)
    • Cui SF, Wang Y, Lv JS, Damu GLV, Zhou CH. Recent advances in application researches of thiazole compounds. Scientia Sinica Chimica 2012; 42: 1105-31 (in Chinese).
    • (2012) Scientia Sinica Chimica , vol.42 , pp. 1105-1131
    • Cui, S.F.1    Wang, Y.2    Lv, J.S.3    Damu, G.L.V.4    Zhou, C.H.5
  • 426
    • 79960284745 scopus 로고    scopus 로고
    • A unique paradigmfor a turn-on near-infrared cyaninebased probe: Noninvasive intravital optical imaging of hydrogen peroxide
    • Karton-Lifshin N, Segal E, Omer L, Portnoy M, Satchi-Fainaro R, Shabat D. A unique paradigmfor a turn-on near-infrared cyaninebased probe: noninvasive intravital optical imaging of hydrogen peroxide. J Am Chem Soc 2011; 133: 10960-5.
    • (2011) J Am Chem Soc , vol.133 , pp. 10960-10965
    • Karton-Lifshin, N.1    Segal, E.2    Omer, L.3    Portnoy, M.4    Satchi-Fainaro, R.5    Shabat, D.6
  • 427
    • 79953787899 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of coumarin-based molecular probes for imaging of myelination
    • Wang CN, Wu CY, Zhu JQ, Miller RH, Wang YM. Design, synthesis, and evaluation of coumarin-based molecular probes for imaging of myelination. J Med Chem 2011; 54: 2331-40.
    • (2011) J Med Chem , vol.54 , pp. 2331-2340
    • Wang, C.N.1    Wu, C.Y.2    Zhu, J.Q.3    Miller, R.H.4    Wang, Y.M.5
  • 428
    • 84862954903 scopus 로고    scopus 로고
    • Myelin imaging compound (MIC) enhanced magnetic resonance imaging of myelination
    • Frullano L, Zhu JQ, Wang CN, Wu CY, Miller RH, Wang YM. Myelin imaging compound (MIC) enhanced magnetic resonance imaging of myelination. J Med Chem 2012; 55: 94-105.
    • (2012) J Med Chem , vol.55 , pp. 94-105
    • Frullano, L.1    Zhu, J.Q.2    Wang, C.N.3    Wu, C.Y.4    Miller, R.H.5    Wang, Y.M.6


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