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Volumn 18, Issue 2, 2013, Pages 1881-1896

Synthesis and antiproliferative activity of C-3 functionalized isobenzofuran-1(3H)-ones

Author keywords

Antiproliferative activity; Isobenzofuran 1(3H) one; Phtalides

Indexed keywords

BENZOFURAN DERIVATIVE; ETOPOSIDE;

EID: 84874614566     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules18021881     Document Type: Article
Times cited : (35)

References (29)
  • 1
    • 84860231411 scopus 로고    scopus 로고
    • A novel antioxidant isobenzofuranone derivative from fungus Cephalosporium sp. AL031
    • Huang, X.-Z.; Zhu, Y.; Guan, X.-L.; Tian, K.; Guo, J.-M.; Wang, H.-B.; Fu, G.-M. A novel antioxidant isobenzofuranone derivative from fungus Cephalosporium sp. AL031. Molecules 2012, 17, 4219-4224.
    • (2012) Molecules , vol.17 , pp. 4219-4224
    • Huang, X.-Z.1    Zhu, Y.2    Guan, X.-L.3    Tian, K.4    Guo, J.-M.5    Wang, H.-B.6    Fu, G.-M.7
  • 2
    • 0037188596 scopus 로고    scopus 로고
    • Isopestacin an isobenzofuranone from Pestalotiopsis microspora possessing antifungal and antioxidant activities
    • Strobel, G.; Ford, E.; Worapong, J.; Harper, J.K.; Arif, A.M.; Grant, D.M.; Fung, P.C.W.; Chau, R.M.W. Isopestacin, an isobenzofuranone from Pestalotiopsis microspora possessing antifungal and antioxidant activities. Phytochemistry 2002, 60, 170-183.
    • (2002) Phytochemistry , vol.60 , pp. 170-183
    • Strobel, G.1    Ford, E.2    Worapong, J.3    Harper, J.K.4    Arif, A.M.5    Grant, D.M.6    Fung, P.C.W.7    Chau, R.M.W.8
  • 3
    • 84858866004 scopus 로고    scopus 로고
    • Antiplatelet activity of 3-butyl-6-bromo-1(3H)- isobenzofuranone on rat platelet aggregation
    • Ma, F.; Gao, Y.; Qiao, H.; Hu, X.; Chang, J. Antiplatelet activity of 3-butyl-6-bromo-1(3H)- isobenzofuranone on rat platelet aggregation. J. Thromb. Thrombolysis 2012, 33, 64-73.
    • (2012) J. Thromb. Thrombolysis , vol.33 , pp. 64-73
    • Ma, F.1    Gao, Y.2    Qiao, H.3    Hu, X.4    Chang, J.5
  • 5
    • 0036163570 scopus 로고    scopus 로고
    • Cryphonectric acid and other minor metabolites from a hypovirulent strain of Cryphonectria parasitica
    • DOI 10.1021/np0103012
    • Arnone, A.; Assante, G.; Nasini, G.; Strada, S.; Vercesi, A. Cryphonectric acid and other minor metabolites from a hypovirulent strain of Cryphonectria parasítica. J. Nat. Prod. 2002, 65, 48-50. (Pubitemid 34118811)
    • (2002) Journal of Natural Products , vol.65 , Issue.1 , pp. 48-50
    • Arnone, A.1    Assante, G.2    Nasini, G.3    Strada, S.4    Vercesi, A.5
  • 10
    • 58949100161 scopus 로고    scopus 로고
    • Synthesis and phytogrowth properties of oxabicyclic analogues related to helminsthosporin
    • Barbosa, L.C.A.; Nogueira, L.B.; Maltha, C.R.A.; Teixeira, R.R.; Silva, A.A. Synthesis and phytogrowth properties of oxabicyclic analogues related to helminsthosporin. Molecules 2009, 14, 160-173.
    • (2009) Molecules , vol.14 , pp. 160-173
    • Barbosa, L.C.A.1    Nogueira, L.B.2    Maltha, C.R.A.3    Teixeira, R.R.4    Silva, A.A.5
  • 12
    • 2942568102 scopus 로고    scopus 로고
    • Regiospecific synthesis of isopestacin, a naturally occurring isobenzofuranone antioxidant
    • DOI 10.1016/j.tetlet.2004.04.175, PII S0040403904010111
    • Pahari, P.; Senapati, B.; Mal, D. Regiospecific synthesis of isopestacin, a naturally occurring isobenzofuranone antioxidante. Tetrahedron Lett. 2004, 45, 5109-5112. (Pubitemid 38759221)
    • (2004) Tetrahedron Letters , vol.45 , Issue.26 , pp. 5109-5112
    • Pahari, P.1    Senapati, B.2    Mal, D.3
  • 13
    • 34948871497 scopus 로고    scopus 로고
    • Regiospecific synthesis of 3-(2,6-dihydroxyphenyl)phthalides: Application to the synthesis of isopestacin and cryphonectric acid
    • DOI 10.1016/j.tet.2007.08.048, PII S0040402007014597
    • Mal, D.; Pahari, P.; De, S.R. Regiospecific synthesis of 3-(2,6-dihydroxyphenyl)phtalides: Application to the synthesis of isopestacin and cryphonectric acid. Tetrahedron 2007, 63, 11781-11792. (Pubitemid 47532148)
    • (2007) Tetrahedron , vol.63 , Issue.47 , pp. 11781-11792
    • Mal, D.1    Pahari, P.2    De, S.R.3
  • 14
    • 0025667792 scopus 로고
    • Synthesis of 1-(2,6-Dihydroxyphenyl)-1-alkanones and Benzophenone by Aromatization of 2-Acyl-3-hydroxy-2-cyclohexene-1-ones with Mercuric Acetate
    • Oliver, J.E.; Wilzer, K.R.; Waters, R.M. Synthesis of 1-(2,6-Dihydroxyphenyl)-1-alkanones and Benzophenone by Aromatization of 2-Acyl-3-hydroxy-2-cyclohexene-1-ones with Mercuric Acetate. Synthesis 1990, 1990, 1117-1119.
    • (1990) Synthesis , vol.1990 , pp. 1117-1119
    • Oliver, J.E.1    Wilzer, K.R.2    Waters, R.M.3
  • 15
    • 0031024171 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • DOI 10.1016/S0169-409X(96)00423-1, PII S0169409X96004231
    • Lipinski, C.A.; Lombardo, F.; Dominy, B.W.; Feeney, P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 1997, 23, 3-25. (Pubitemid 27046991)
    • (1997) Advanced Drug Delivery Reviews , vol.23 , Issue.1-3 , pp. 3-25
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 17
    • 27344449477 scopus 로고    scopus 로고
    • Computing chemistry on the web
    • DOI 10.1016/S1359-6446(05)03584-1, PII S1359644605035841
    • Tetko, I.V. Computing chemistry on the web. Drug Discov. Today 2005, 10, 1497-1500. (Pubitemid 41527191)
    • (2005) Drug Discovery Today , vol.10 , Issue.22 , pp. 1497-1500
    • Tetko, I.V.1
  • 18
    • 84857192927 scopus 로고    scopus 로고
    • (accessed on September 2012)
    • Molinspiration Cheminformatics. Available online: http://www. molinspiration.com/(accessed on September 2012).
    • Molinspiration Cheminformatics
  • 19
    • 84861643477 scopus 로고    scopus 로고
    • Quinazoline-etyrphostin as a new class of antitumor agents, molecular properties prediction, synthesis and biological testing
    • Alafeefy, A.M.; Alqasoumi, S.I.; Ashour, A.E.; Masand, V.; Al-Jaber, N.A.; Hadda, T.B.; Mohameda, M.A. Quinazoline-etyrphostin as a new class of antitumor agents, molecular properties prediction, synthesis and biological testing. Eur. J. Med. Chem. 2012, 53, 133-140.
    • (2012) Eur. J. Med. Chem. , vol.53 , pp. 133-140
    • Alafeefy, A.M.1    Alqasoumi, S.I.2    Ashour, A.E.3    Masand, V.4    Al-Jaber, N.A.5    Hadda, T.B.6    Mohameda, M.A.7
  • 20
    • 84861904904 scopus 로고    scopus 로고
    • Predictions and correlations of structure activity relationship of some aminoantipyrine derivatives on the basis of theoretical and experimental ground
    • Ali, P.; Meshram, J.; Sheikh, J.; Tiwari, V.; Dongre, R.; Hadda, T.B. Predictions and correlations of structure activity relationship of some aminoantipyrine derivatives on the basis of theoretical and experimental ground. Med. Chem. Res. 2012, 21, 157-164.
    • (2012) Med. Chem. Res. , vol.21 , pp. 157-164
    • Ali, P.1    Meshram, J.2    Sheikh, J.3    Tiwari, V.4    Dongre, R.5    Hadda, T.B.6
  • 22
    • 77954348444 scopus 로고    scopus 로고
    • Metal based biologically active compounds: Design, Synthesis, and antibacterial/antifungal/cytotoxic properties of triazole-derived Schiff bases and their oxovanadium(IV) complexes
    • Chohan, Z.H.; Sumrra, S.H.; Youssoufi, M.H.; Hadda, T.B. Metal based biologically active compounds: Design, synthesis, and antibacterial/antifungal/ cytotoxic properties of triazole-derived Schiff bases and their oxovanadium(IV) complexes. Eur. J. Med. Chem. 2010, 45, 2739-2747.
    • (2010) Eur. J. Med. Chem. , vol.45 , pp. 2739-2747
    • Chohan, Z.H.1    Sumrra, S.H.2    Youssoufi, M.H.3    Hadda, T.B.4
  • 23
    • 13244266921 scopus 로고    scopus 로고
    • Lead- and drug-like compounds: The rule-of-five revolution
    • DOI 10.1016/j.ddtec.2004.11.007, PII S1740674904000551
    • Lipinski, C.A. Lead- and drug-like compounds: The rule-of-five revolution. Drug Discov. Today Technol. 2004, 1, 337-341. (Pubitemid 40186335)
    • (2004) Drug Discovery Today: Technologies , vol.1 , Issue.4 , pp. 337-341
    • Lipinski, C.A.1
  • 24
    • 0037124196 scopus 로고    scopus 로고
    • Drugs leads, and drug-likeness: An analysis of some recently launched drugs
    • Proudfoot, R. Drugs, leads, and drug-likeness: An analysis of some recently launched drugs. Bioorg. Med. Chem. Lett. 2012, 12, 1647-1650.
    • (2012) Bioorg. Med. Chem. Lett. , vol.12 , pp. 1647-1650
    • Proudfoot, R.1
  • 25
    • 84866141196 scopus 로고    scopus 로고
    • Petra Osiris and molinspiration (POM) together as a successful support in drug design: Antibacterial activity and biopharmaceutical characterization of some azo schiff bases
    • Jarrahpour, A.; Fathi, J.; Mimouni, M.; Hadda, T.B.; Sheikh, J.; Chohan, Z.; Parvez, A. Petra, Osiris and molinspiration (POM) together as a successful support in drug design: Antibacterial activity and biopharmaceutical characterization of some azo schiff bases. Med. Chem. Res. 2012, 21, 1984-1990.
    • (2012) Med. Chem. Res. , vol.21 , pp. 1984-1990
    • Jarrahpour, A.1    Fathi, J.2    Mimouni, M.3    Hadda, T.B.4    Sheikh, J.5    Chohan, Z.6    Parvez, A.7
  • 26
    • 84864035147 scopus 로고    scopus 로고
    • In silico modification of suberoylanilide hydroxamic acid (SAHA) as potential inhibitor for class II histone deacetylase (HDAC)
    • Tambunan, U.S.F.; Bramantya, N.; Parikesit, A.A. In silico modification of suberoylanilide hydroxamic acid (SAHA) as potential inhibitor for class II histone deacetylase (HDAC). BMC Bioinformatics 2011, 12, S13-S23.
    • (2011) BMC Bioinformatics , vol.12
    • Tambunan, U.S.F.1    Bramantya, N.2    Parikesit, A.A.3
  • 27
    • 0035289779 scopus 로고    scopus 로고
    • Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings
    • DOI 10.1016/S0169-409X(00)00129-0, PII S0169409X00001290
    • Lipinski, C.A.; Lombardo, F.; Dominy, B.W.; Feeney, P.J. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv. Drug Deliv. Rev. 2001, 46, 3-26. (Pubitemid 33653411)
    • (2000) Advanced Drug Delivery Reviews , vol.46 , Issue.1-3 , pp. 3-26
    • Lipinski, C.A.1    Lombardo, F.2    Dominy, B.W.3    Feeney, P.J.4
  • 28
    • 0032795192 scopus 로고    scopus 로고
    • Rapid calculation of polar molecular surface area and its application to the prediction of transport phenomena. 1. Prediction of intestinal absorption
    • DOI 10.1021/js9804011
    • Clark, D.E. Rapid calculation of polar molecular surface area and its application to the prediction of transport phenomena. 1. Prediction of Intestinal Absorption. J. Pharm. Sci. 1999, 88, 807-814. (Pubitemid 29398550)
    • (1999) Journal of Pharmaceutical Sciences , vol.88 , Issue.8 , pp. 807-814
    • Clark, D.E.1
  • 29
    • 0034609833 scopus 로고    scopus 로고
    • Fast calculation of molecular polar surface area as a sum of fragment-based contributions and its application to the prediction of drug transport properties
    • Ertl, P.; Rohde, B.; Selzer, P. Fast Calculation of Molecular Polar Surface Area as a Sum of Fragment-Based Contributions and Its Application to the Prediction of Drug Transport Properties. J. Med. Chem. 2000, 43, 3714-3717.
    • (2000) J. Med. Chem. , vol.43 , pp. 3714-3717
    • Ertl, P.1    Rohde, B.2    Selzer, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.