메뉴 건너뛰기




Volumn 18, Issue 31, 2011, Pages 4786-4812

Quinazolinone analogs as potential therapeutic agents

Author keywords

Heterocycles; Pharmacological significance; Quinazolinone

Indexed keywords

2 [(3,6 DIOXOPYRIDAZIN 4 YL)THIO] 3 BENZYL 4 OXO 6 IODO 3H QUINAZOLINE; 2 [2 HYDROXY 3 METHOXYPHENYL] 3 [HYDROXYL 3 METHOXYBENZYLAMINO] 1,2 DIHYDROQUINAZOLIN 4(3H) ONE; 2 PHENOXYMETHYL 3H QUINAZOLIN 4 ONE; 2(1H) QUINAZOLINONE (1H 1,3 QUINAZOLIN 2 ONE); 2,4(1H,3H) QUINAZOLINEDIONE (1H,3H 1,3 QUINAZOLINE 2,4 DIONE); 3 (3,4,5 TRIMETHOXYBENZYLIDENEAMINO) 6,8 DIBROMO 2 PHENYLQUINAZOLIN 4(3H) ONE; 3,4 DIHYDRO 1H,6H [1,4] OXAZINO [3,4 B] QUINAZOLIN 6 ONE; 4(3H) QUINAZOLINONE (3H 1,3 QUINAZOLIN 4 ONE); 6 CHLORO 2 STYRYL 3 (PYRIMIDIN 2 YL) 4(3H) QUINAZOLINONE; AMINOQUINAZOLINONE DERIVATIVE; AMPHOTERICIN; AMPICILLIN; ANTIBIOTIC AGENT; ANTICONVULSIVE AGENT; ANTIFUNGAL AGENT; ANTIMALARIAL AGENT; ANTINEOPLASTIC AGENT; ANTIVIRUS AGENT; CHOLINESTERASE INHIBITOR; COLCHICINE; CYCLIN DEPENDENT KINASE INHIBITOR; DOXORUBICIN; FLUCONAZOLE; ITRACONAZOLE; N BENZOYL N' [2 (3 BENZYL 4 OXO6 IODO 3H QUINOZOLIN 2 YL)THIOACETYL]HYDRAZINE; N' [(3 BENZYL 4 OXO 6 IODO 3H QUINAZOLIN 2 YL) THIOACETYL] N 3 ETHYLTHIOSEMICARBAZIDE; NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR; NORFLOXACIN; QUINAZOLINE; QUINAZOLINONE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 80054859208     PISSN: 09298673     EISSN: 1875533X     Source Type: Journal    
DOI: 10.2174/092986711797535326     Document Type: Article
Times cited : (81)

References (192)
  • 1
    • 34548035847 scopus 로고    scopus 로고
    • Rapid synthesis of 2,3-disubstituted-quinazolin-4-ones enhanced by microwave-assisted decomposition of formamide
    • DOI 10.1016/j.tetlet.2007.07.114, PII S0040403907014475
    • Kostakis, I.K.; Elomri, A.; Seguin, E.; Iannelli, M.; Besson, T. Rapid synthesis of 2,3-disubstituted-quinazolin-4-ones enhanced by microwave assisted decomposition of formamide. Tetrahedron lett., 2007, 48, 6609-6613. (Pubitemid 47284260)
    • (2007) Tetrahedron Letters , vol.48 , Issue.38 , pp. 6609-6613
    • Kostakis, I.K.1    Elomri, A.2    Seguin, E.3    Iannelli, M.4    Besson, T.5
  • 2
    • 35948973607 scopus 로고    scopus 로고
    • Antibacterial activity of some 3- (Arylideneamino)-2-phenylquinazolin- 4(3H)-ones: Synthesis and preliminary QSAR studies
    • Nanda, A.K.; Ganguli, S.; Chakraborty, R. Antibacterial activity of some 3- (Arylideneamino)-2-phenylquinazolin-4(3H)-ones: Synthesis and preliminary QSAR studies. Molecules, 2007, 12, 2413-2426.
    • (2007) Molecules , vol.12 , pp. 2413-2426
    • Nanda, A.K.1    Ganguli, S.2    Chakraborty, R.3
  • 3
    • 51449083986 scopus 로고    scopus 로고
    • Synthesis of tryptanthrin and deoxyvascinone by regioselective lithiation-intramolecular electrophillic reaction approach
    • Potewar, T.M.; Ingale, S.A.; Srinivasan, K.V. Synthesis of tryptanthrin and deoxyvascinone by regioselective lithiation-intramolecular electrophillic reaction approach. ARKIVOC, 2008, xiv, 100-108.
    • (2008) ARKIVOC , vol.14 , pp. 100-108
    • Potewar, T.M.1    Ingale, S.A.2    Srinivasan, K.V.3
  • 4
    • 77950132719 scopus 로고    scopus 로고
    • Synthesis and anticoccidial activity of 4-(2-methoxyphenyl)-2- oxobutylquinazolinone derivatives
    • You, J.; Ye, C.; Weng, Y.; Mo, X.; Wang, Y. Synthesis and anticoccidial activity of 4-(2-methoxyphenyl)-2-oxobutylquinazolinone derivatives. ARKIVOC, 2008, xvii, 1-11.
    • (2008) ARKIVOC , vol.17 , pp. 1-11
    • You, J.1    Ye, C.2    Weng, Y.3    Mo, X.4    Wang, Y.5
  • 7
    • 51449122251 scopus 로고    scopus 로고
    • Design synthesis and potential CNS activity of some novel 1-(4-substituted-phenyl)-3-(4-oxo-2- propyl-4H-quinazolin-3-yl)-urea
    • Kashaw, KS.; Kashaw, V.; Mishra, P.; Jain, N.K. Design, synthesis and potential CNS activity of some novel 1-(4-substituted-phenyl)-3-(4-oxo-2- propyl-4H-quinazolin-3-yl)-urea. ARKIVOC, 2008, 15, 17-26.
    • (2008) ARKIVOC , vol.15 , pp. 17-26
    • Kashaw, K.S.1    Kashaw, V.2    Mishra, P.3    Jain, N.K.4
  • 9
    • 22244463536 scopus 로고    scopus 로고
    • Synthesis, characterization and primary antimicrobial activity evaluation of 3-phenyl-6-methyl-4(3H)-quinazolinone-2-yl-mercaptoacetic acid arylidenehydrazides
    • Gursoy, A.; Unal, B.; Karali, N.; Otuk, G. Synthesis, characterization and primary antimicrobial activity evaluation of 3-Phenyl-6-methyl-4(3H)- quinazolinone-2-yl-mercaptoacetic acid arylidenehydrazides. Turk. J. Chem., 2005, 29, 233-245. (Pubitemid 40993194)
    • (2005) Turkish Journal of Chemistry , vol.29 , Issue.3 , pp. 233-245
    • Gursoy, A.1    Unal, B.2    Karali, N.3    Otuk, G.4
  • 13
    • 43049086303 scopus 로고    scopus 로고
    • A microwave assisted and heteropolyacids-catalysed cyclocondensation reaction for the synthesis of 4(3H)-quinazolinones
    • Ighilahriz, K.; Boutemeur, B.; Chami, F.; Rabia, C.; Hamdi, M.; Hamdi, S.M. A microwave assisted and heteropolyacids-catalysed cyclocondensation reaction for the synthesis of 4(3H)-quinazolinones. Molecules, 2008, 13, 779-789.
    • (2008) Molecules , vol.13 , pp. 779-789
    • Ighilahriz, K.1    Boutemeur, B.2    Chami, F.3    Rabia, C.4    Hamdi, M.5    Hamdi, S.M.6
  • 14
    • 33646403467 scopus 로고    scopus 로고
    • Microwave assisted synthesis of N-arylheterocyclic substituted-4- aminoquinazoline derivatives
    • DOI 10.3390/11040272
    • Liu, G.; Yang, S.; Song, B.; Xue, W.; Hu, D.; Jin, L.; Lu, P. Microwave assisted synthesis of N-arylheterocyclic substituted-4-aminoquinazoline derivatives. Molecules, 2006, 11, 272-278. (Pubitemid 43684789)
    • (2006) Molecules , vol.11 , Issue.4 , pp. 272-278
    • Liu, G.1    Yang, S.2    Song, B.3    Xue, W.4    Hu, D.5    Jin, L.6    Lu, P.7
  • 15
    • 84862754116 scopus 로고    scopus 로고
    • Cancer from Wikipedia, the free encyclopedia Accessed on February rfvn1 24 2010)
    • Cancer from Wikipedia, the free encyclopedia. http://en.wikipedia.org/ wiki /cancer. (Accessed on February 24, 2010).
  • 16
    • 1942438028 scopus 로고    scopus 로고
    • Microtubules as a target for anticancer drugs
    • 253-264
    • Jordan, M.A.; Wilson, L. Microtubules as a target for anticancer drugs. Nat. Rev., 2004, 4, 253ć264.
    • (2004) Nat. Rev. , vol.4
    • Jordan, M.A.1    Wilson, L.2
  • 17
    • 75749146640 scopus 로고    scopus 로고
    • Cytotoxic activity and threedimensional quantitative structure activity relationship of 2-aryl-1 8- naphthyridin-4-ones
    • 511ć516
    • Kim, Y.J.; Kim, A.E.; Chung, M.L.; Im, C. Cytotoxic activity and threedimensional quantitative structure activity relationship of 2-aryl-1,8- naphthyridin-4-ones. Korean J. Physiol. Pharmacol., 2009, 13, 511ć516.
    • (2009) Korean J. Physiol. Pharmacol. , vol.13
    • Kim, Y.J.1    Kim, A.E.2    Chung, M.L.3    Im, C.4
  • 18
    • 46749097971 scopus 로고    scopus 로고
    • Antiproliferative activity and apoptosis induced by6-bromo-2-(morpholin- 1- yl)-4-amlinoquinazoline on cells of leukemia lines
    • Jantova, S.; Repicky, A.; Paulovicova, E.; Letasiova, S.; Cipak, L. Antiproliferative activity and apoptosis induced by 6-bromo-2-(morpholin-1- yl)-4-anilinoquinazoline on cells of leukemia lines. Exp. Oncol., 2008, 30(2), 139-142. (Pubitemid 351951391)
    • (2008) Experimental Oncology , vol.30 , Issue.2 , pp. 139-142
    • Jantova, S.1    Repicky, A.2    Paulovicova, E.3    Letasiova, S.4    Cipak, L.5
  • 19
    • 34248157771 scopus 로고    scopus 로고
    • Growth inhibition and apoptosis induced by 2-phenoxymethyl-3H-quinazolin- 4- one in HL-60 leukemia cells
    • Cipak, L.; Repicky, A.; Jantova, S. Growth inhibition and apoptosis induced by 2-phenoxymethyl-3H-quinazolin-4-one in HL-60 leukemia cells. Exp. Oncol., 2007, 29(1), 13-17. (Pubitemid 46713473)
    • (2007) Experimental Oncology , vol.29 , Issue.1 , pp. 13-17
    • Cipak, L.1    Repicky, A.2    Jantova, S.3
  • 20
    • 0037032835 scopus 로고    scopus 로고
    • The protein kinase complement of the human genome
    • DOI 10.1126/science.1075762
    • Manning, G.; Whyte, D.B.; Martinez, R.; Hunter, T.; Sundersanam, S. The protein kinase complement of the human genome. Science., 2002, 298, 1912-1934. (Pubitemid 35425239)
    • (2002) Science , vol.298 , Issue.5600 , pp. 1912-1934
    • Manning, G.1    Whyte, D.B.2    Martinez, R.3    Hunter, T.4    Sudarsanam, S.5
  • 21
    • 45949085044 scopus 로고    scopus 로고
    • Novel 9-oxo-thiazolo[5,4-f]quinazoline-2-carbonitrile derivatives as dual cyclin-dependent kinase 1 (CDK1)/glycogen synthase kinase-3 (GSK-3) inhibitors: Synthesis, biological evaluation and molecular modeling studies
    • DOI 10.1016/j.ejmech.2007.09.020, PII S0223523407003558
    • Loge, C.; Testard, A.; Thiery, V.; Lozach, O.; Blairvacq, M.; Robert, M..J.; Meijer, L.; Besson, T. Novel 9-oxo-thiazolo[5,4-f]quinazoline-2- carbonitrile derivatives as dual cyclin-dependent kinase 1 (CDK1)/glycogen synthase kinase-3 (GSK-3) inhibitors: Synthesis, biological evaluation and molecular modeling studies. Eur. J. Med. Chem., 2008, 43, 1469-1477. (Pubitemid 351890437)
    • (2008) European Journal of Medicinal Chemistry , vol.43 , Issue.7 , pp. 1469-1477
    • Loge, C.1    Testard, A.2    Thiery, V.3    Lozach, O.4    Blairvacq, M.5    Robert, J.-M.6    Meijer, L.7    Besson, T.8
  • 22
    • 79953073824 scopus 로고    scopus 로고
    • In Silico screening, synthesis and in vitro evaluation of some quinazolinone and pyridine derivatives as dihydrofolate reductase inhibitors for anticancer activity
    • Nerker, A.G.; Saxena, A.K.; Ghone, S.A.; Thaker, A.K. In Silico screening, synthesis and in vitro evaluation of some quinazolinone and pyridine derivatives as dihydrofolate reductase inhibitors for anticancer activity. E J. Chem., 2009, 6(1), 97-102.
    • (2009) E J. Chem. , vol.6 , Issue.1 , pp. 97-102
    • Nerker, A.G.1    Saxena, A.K.2    Ghone, S.A.3    Thaker, A.K.4
  • 23
    • 0029989812 scopus 로고    scopus 로고
    • Heterocondensed quinazolones: Synthesis and protein-tyrosine kinase inhibitory activity of 3,4-dihydro-lH,6H- [1,4]oxazino-[3,4-b] quinazolin-6- one derivatives
    • Orfi, L.; Kokosi, J.; Szasz, G.; Kovesdi, I.; Mak, M.; Teplan, I.; Keri, G. Heterocondensed quinazolones: Synthesis and protein-tyrosine kinase inhibitory activity of 3,4-dihydro-lH,6H- [1,4]oxazino-[3,4-b] quinazolin-6- one derivatives. Bioorg. Med. Chem., 1996, 4(4), 547-551.
    • (1996) Bioorg. Med. Chem. , vol.4 , Issue.4 , pp. 547-551
    • Orfi, L.1    Kokosi, J.2    Szasz, G.3    Kovesdi, I.4    Mak, M.5    Teplan, I.6    Keri, G.7
  • 24
    • 0038711948 scopus 로고    scopus 로고
    • Substituted quinazolines, part 2. Synthesis and in-vitro anticancer evaluation of new 2-substituted mercapto-3H-quinazoline analogs
    • DOI 10.1002/ardp.200390011
    • Khalil, A.A.; Hamide, S.G.A.; Al-Obaid, A.M.; El-Subbagh, H.I. Substituted quinazolines, Part 2. Synthesis and in vitro anticancer evaluation of new 2- substituted mercapto-3H-quinazoline analogs. Arch. Pharm. Pharm. Med. Chem., 2003, 2, 95-103. (Pubitemid 36547177)
    • (2003) Archiv der Pharmazie , vol.336 , Issue.2 , pp. 95-103
    • Khalil, A.A.1    Abdel Hamide, S.G.2    Al-Obaid, A.M.3    El-Subbagh, H.I.4
  • 25
    • 33744801227 scopus 로고    scopus 로고
    • Computer aided design of selective COX-2 inhibitors: Molecular docking of structurally diverse cyclooxygenase-2 inhibitors using FlexX#. Internet Electron
    • Chakraborty, A.K.; Thilagavathi, R. Computer aided design of selective COX-2 inhibitors: Molecular docking of structurally diverse cyclooxygenase-2 inhibitors using FlexX#. Internet Electron. J. Mol Des., 2004, 3(11), 704-719.
    • (2004) J. Mol Des. , vol.3 , Issue.11 , pp. 704-719
    • Chakraborty, A.K.1    Thilagavathi, R.2
  • 26
  • 27
    • 0034525453 scopus 로고    scopus 로고
    • Synthesis and in vitro antitumour activity evaluation of 1-aryl-1H,3H-thiazolo[4,3-b]quinazolines
    • DOI 10.1016/S0223-5234(00)01195-8
    • Grasso, S.; Micalea, N.; Monforteb, A.N.; Monfortea, P.; Polimenia, S.; Zappala, M. Synthesis and in vitro antitumour activity evaluation of 1-aryl- 1H,3H-thiazolo[4,3-b]quinazolines. Eur. J. Med. Chem., 2000, 35, 1115-1119. (Pubitemid 32050018)
    • (2000) European Journal of Medicinal Chemistry , vol.35 , Issue.12 , pp. 1115-1119
    • Grasso, S.1    Micale, N.2    Monforte, A.-M.3    Monforte, P.4    Polimeni, S.5    Zappala, M.6
  • 28
    • 0003986004 scopus 로고    scopus 로고
    • 5th ed.; Jaypee Brothers; medical publishers (P) Ltd: New Delhi
    • Tripathi, K.D. Essentials of Medical Pharmacology. 5th ed.; Jaypee Brothers; medical publishers (P) Ltd: New Delhi. 2004, pp. 767.
    • (2004) Essentials of Medical Pharmacology , pp. 767
    • Tripathi, K.D.1
  • 29
    • 0025302762 scopus 로고
    • Synthesis and biological evaluation of 2-styrylquinazolin-4(3H)-ones, a new class of antimitotic anticancer agents which inhibit tubulin polymerization
    • DOI 10.1021/jm00168a029
    • Jiang, J.B.; Hesson, D.P., Dusak, B.A.; Dexter, D.L.; Kang, G.J; Hamel, E. Synthesis and biological evaluation of 2-styrylquinazolin-4(3H)-ones, a new class of antimitotic anticancer agents which inhibit tubulin polymerization. J. Med. Chem., 1990, 33, 1721-1728. (Pubitemid 20180634)
    • (1990) Journal of Medicinal Chemistry , vol.33 , Issue.6 , pp. 1721-1728
    • Jiang, J.B.1    Hesson, D.P.2    Dusak, B.A.3    Dexter, D.L.4    Kang, G.J.5    Hamel, E.6
  • 30
    • 49449111557 scopus 로고    scopus 로고
    • Asymmetric synthesis of 2,3- dihydro-2-arylquinazolin-4-ones: Methodology and application to a potent fluorescent tubulin inhibitor with anticancer activity
    • Chinigo, GM.; Paige, M.; Grindrod, S.; Hamel, E.; Dakshanamurthy, S.; Chruszcz, M.; Minor, W.; Brown, M.L. Asymmetric synthesis of 2,3- dihydro-2-arylquinazolin-4-ones: Methodology and application to a potent fluorescent tubulin inhibitor with anticancer activity. J. Med. Chem., 2008, 51(15), 4620-4631.
    • (2008) J. Med. Chem. , vol.51 , Issue.15 , pp. 4620-4631
    • Chinigo, G.M.1    Paige, M.2    Grindrod, S.3    Hamel, E.4    Dakshanamurthy, S.5    Chruszcz, M.6    Minor, W.7    Brown, M.L.8
  • 31
    • 0034676319 scopus 로고    scopus 로고
    • 6-alkylamino- and 2,3-dihydro-3′-methoxy-2-phenyl-4-quinazolinones and related compounds: Their synthesis, cytotoxicity, and inhibition of tubulin polymerization
    • DOI 10.1021/jm000151c
    • Hour, M.J.; Huang, L.J.; Kuo, S.C.; Xia, Y.; Bastow, K.; Nakanishi, Y.; Hamel, E.; Lee, K.H. 6-Alkylamino- and 2,3-dihydro-3'-methoxy-2-phenyl- 4-quinazolinenones and related compounds: Their synthesis, cytotoxicity and inhibition of tubulin polymerization. J. Med. Chem., 2000, 43, 4479-4487. (Pubitemid 32046872)
    • (2000) Journal of Medicinal Chemistry , vol.43 , Issue.23 , pp. 4479-4487
    • Hour, M.-J.1    Huang, L.-J.2    Kuo, S.-C.3    Xia, Y.4    Bastow, K.5    Nakanishi, Y.6    Hamel, E.7    Lee, K.-H.8
  • 33
    • 1842557498 scopus 로고    scopus 로고
    • Synthesis, cytotoxicity, and inhibitory effects on tubulin polymerization of a new 3-heterocyclo substituted 2-styrylquinazolinones
    • DOI 10.1016/j.ejmech.2003.12.009, PII S0223523404000091
    • Raffa, D.; Edler, M.C.; Daidone, G.; Maggio, B.; Merickech, M.; Plescia, S.; Schillaci, D.; Bai, R.; Hamel, E. Synthesis, cytotoxicity, and inhibitory effects on tubulin polymerization of a new 3-heterocyclo substituted 2- styrylquinazolinones. Eur. J. Med. Chem., 2004, 39, 299-304. (Pubitemid 38457024)
    • (2004) European Journal of Medicinal Chemistry , vol.39 , Issue.4 , pp. 299-304
    • Raffa, D.1    Edler, M.C.2    Daidone, G.3    Maggio, B.4    Merickech, M.5    Plescia, S.6    Schillaci, D.7    Bai, R.8    Hamel, E.9
  • 35
    • 0026073108 scopus 로고
    • Boron containing thiouracil derivatives for neutron capture therapy of melanoma
    • Tjarks, W.; Gabel, D. Boron containing thiouracil derivatives for neutron capture therapy of melanoma. J. Med. Chem.,1991, 34, 315-319.
    • (1991) J. Med. Chem. , vol.34 , pp. 315-319
    • Tjarks, W.1    Gabel, D.2
  • 37
    • 0030021606 scopus 로고    scopus 로고
    • Synthesis and biological properties of carboranylaziridines bearing cascade polyols
    • DOI 10.1016/0960-894X(95)00545-5
    • Yamato, Y.; Sadayori, N. Synthesis and biological properties of carboranyl aziridines bearing cascade polyols. Bioorg. Med. Chem. Lett., 1996, 6(1), 9-12. (Pubitemid 26024281)
    • (1996) Bioorganic and Medicinal Chemistry Letters , vol.6 , Issue.1 , pp. 9-12
    • Yamamoto, Y.1    Sadayori, N.2
  • 38
    • 57949099982 scopus 로고    scopus 로고
    • Promising carboranyl quinazolines for boron neutron capture therapy: Synthesis, characterization, and in vitro toxicity evaluation
    • Genady, A.R. Promising carboranyl quinazolines for boron neutron capture therapy: Synthesis, characterization, and in vitro toxicity evaluation. Eur. J. Med. Chem., 2009, 44, 409-416.
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 409-416
    • Genady, A.R.1
  • 40
    • 84862754114 scopus 로고    scopus 로고
    • World Health Organisation Report on infectious diseases: Removing obstacles to healthy development. Geneva, Switzerland: World Health Organization (Accessed on July 24 2010)
    • World Health Organisation (1999). Report on infectious diseases: Removing obstacles to healthy development. Geneva, Switzerland: World Health Organization. http://www.who.int/infectious-disease-report/index-rpt99.html (Accessed on July 24, 2010).
    • (1999)
  • 41
    • 77954398940 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of certain novel 1- cyclopropyl-6-flouro-1,4-dihydro-7-4-substituted-piperazin-1-yl-4- oxoquinolin-3-carboxylates
    • Sharma, P.C.; Jain, S. Synthesis and antibacterial activity of certain novel 1- cyclopropyl-6-flouro-1,4-dihydro-7-4-substituted-piperazin-1-yl-4- oxoquinolin-3-carboxylates. Acta Pharm. Sciencia, 2008, 50, 35-40.
    • (2008) Acta Pharm. Sciencia , vol.50 , pp. 35-40
    • Sharma, P.C.1    Jain, S.2
  • 42
    • 76749128125 scopus 로고    scopus 로고
    • Microwave assisted synthesis of some novel 2-pyrazoline derivatives as possible antimicrobial agents
    • Chawla, R.; Sahoo, U.; Arora, A.; Sharma, P.C.; Radhakrishnan, V. Microwave assisted synthesis of some novel 2-pyrazoline derivatives as possible antimicrobial agents. Acta Pol. Pharm. Drug Res., 2010, 67(1), 55-61.
    • (2010) Acta Pol. Pharm. Drug Res , vol.67 , Issue.1 , pp. 55-61
    • Chawla, R.1    Sahoo, U.2    Arora, A.3    Sharma, P.C.4    Radhakrishnan, V.5
  • 44
    • 74949119366 scopus 로고    scopus 로고
    • Flouroquinoline antibacterials: A review on chemistry, microbiology and therapeutic prospects
    • Sharma, P.C.; Jain A.; Jain, S. Flouroquinoline antibacterials: A review on chemistry, microbiology and therapeutic prospects. Acta Pol. Pharm. Drug Res., 2009, 66(6), 587-604.
    • (2009) Acta Pol. Pharm. Drug Res. , vol.66 , Issue.6 , pp. 587-604
    • Sharma, P.C.1    Jain, A.2    Jain, S.3
  • 46
    • 77954393125 scopus 로고    scopus 로고
    • Ciprofloxacin: Review on developments in synthetic, analytical and medicinal aspects
    • Sharma, P.C.; Jain, A.; Jain, S.; Pahwa, R.; Yar, M.S. Ciprofloxacin: Review on developments in synthetic, analytical and medicinal aspects. J. Enz. Inhib. Med. Chem., 2010, 25(4), 577-589.
    • (2010) J. Enz. Inhib. Med. Chem , vol.25 , Issue.4 , pp. 577-589
    • Sharma, P.C.1    Jain, A.2    Jain, S.3    Pahwa, R.4    Yar, M.S.5
  • 47
    • 56849095920 scopus 로고    scopus 로고
    • Synthesis and in vitro antibacterial activity of some novel N-nicotinyl-1-ethyl-6-flouro-1,4-dihyro-7-piperazin-1-yl-4- oxoquinoline-3- carboxylates
    • Sharma, PC.; Jain, S. Synthesis and in vitro antibacterial activity of some novel N-nicotinyl-1-ethyl-6-flouro-1,4-dihyro-7-piperazin-1-yl-4- oxoquinoline-3-carboxylates. Acta Pol. Pharm. Drug Res., 2008, 65(5), 551-586.
    • (2008) Acta Pol. Pharm. Drug Res. , vol.65 , Issue.5 , pp. 551-586
    • Sharma, P.C.1    Jain, S.2
  • 48
    • 77950816432 scopus 로고    scopus 로고
    • Design and biological evaluation of biphenyl-4-carboxylic acid hydrazidehydrazone for antimicrobial activity
    • Aakashdeep.; Jain, S.; Sharma, P.C.; Verma, P.; Kumar, M.; Dora, C.P. Design and biological evaluation of biphenyl-4-carboxylic acid hydrazidehydrazone for antimicrobial activity. Acta Pol. Pharm. Drug Res., 2010, 67(3), 255-259.
    • (2010) Acta Pol. Pharm. Drug Res. , vol.67 , Issue.3 , pp. 255-259
    • Aakashdeep Jain, S.1    Sharma, P.C.2    Verma, P.3    Kumar, M.4    Dora, C.P.5
  • 50
    • 46349108660 scopus 로고    scopus 로고
    • 3D-QSAR CoMFA study of some heteroarylpyrroles as possible anticandida agents
    • DOI 10.4103/0250-474X.41447
    • Sharma, P.C.; Sharma, S.V.; Sharma, A.; Suresh, B. 3D-QSAR CoMFA study of some heteroarylpyrroles as possible anticandida agents. Indian J. Pharm. Sci., 2008, 70(2), 154-158. (Pubitemid 351920188)
    • (2008) Indian Journal of Pharmaceutical Sciences , vol.70 , Issue.2 , pp. 154-158
    • Sharma, P.1    Sharma, S.2    Sharma, A.3    Suresh, B.4
  • 51
    • 0032771518 scopus 로고    scopus 로고
    • In-vitro comparative activity of UR-9825, itraconazole and fluconazole against clinical isolates of Candida spp
    • DOI 10.1093/jac/44.2.283
    • Ramos, G.; Estrella, M.C.; Monzon, A.; Tudela, J.L. In vitro comparative activity of UR-9825, itraconazole and fluconazole against clinical isolates of Candida spp. J. Antimicrob. Chemother., 1999, 44, 283-286. (Pubitemid 29389293)
    • (1999) Journal of Antimicrobial Chemotherapy , vol.44 , Issue.2 , pp. 283-286
    • Ramos, G.1    Cuenca-Estrella, M.2    Monzon, A.3    Rodriguez-Tudela, J.L.4
  • 52
    • 79952092698 scopus 로고    scopus 로고
    • Microwave assisted efficient synthesis and anti-fungal evaluation of some NPhenyl- 3-(substituted phenyl) propenamides
    • Sharma, P.C.; Sharma, S.V.; Shrishailappa, B.; Sharma, A.; Suresh, B. Microwave assisted efficient synthesis and anti-fungal evaluation of some NPhenyl- 3-(substituted phenyl) propenamides. Indian J. Pharm. Edu. Res., 2007, 41(2), 140-145.
    • (2007) Indian J. Pharm. Edu. Res. , vol.41 , Issue.2 , pp. 140-145
    • Sharma, P.C.1    Sharma, S.V.2    Shrishailappa, B.3    Sharma, A.4    Suresh, B.5
  • 53
    • 62649093569 scopus 로고    scopus 로고
    • Synthesis of some new isoxazoline derivatives as possible anti-candida agents
    • Sharma, P.C.; Sharma, S.V.; Jain, S.; Singh, S.; Suresh, B. Synthesis of some new isoxazoline derivatives as possible anti-candida agents. Acta Pol. Pharm. Drug Res., 2009, 66(1), 101-104.
    • (2009) Acta Pol. Pharm. Drug Res. , vol.66 , Issue.1 , pp. 101-104
    • Sharma, P.C.1    Sharma, S.V.2    Jain, S.3    Singh, S.4    Suresh, B.5
  • 54
    • 79851483355 scopus 로고    scopus 로고
    • Pharmacological significance of triazole scaffold
    • doi: 10.3109/14756360903524304
    • Kharb, R.; Sharma, P.C.; Yar, M.S. Pharmacological significance of triazole scaffold. J. Enz. Inhib. Med. Chem., 2011, 26(1), 1-21. doi: 10.3109/14756360903524304.
    • (2011) J. Enz. Inhib. Med. Chem. , vol.26 , Issue.1 , pp. 1-21
    • Kharb, R.1    Sharma, P.C.2    Yar, M.S.3
  • 57
    • 34347370890 scopus 로고    scopus 로고
    • AntiHIV, antibacterial and antifungal activities of some novel 2-methyl-3-(substituted methylamino)-(3H)-quinazolin-4-ones
    • Algarswamy, V.; Murugesan, S.; Dhanabal, K.; Murugan, M.; Cercq, D.E. Anti HIV, antibacterial and antifungal activities of some novel 2-methyl-3- (substituted methylamino)-(3H)-quinazolin-4-ones. Indian J. Pharm. Sci., 2007, 69(2), 304-307. (Pubitemid 47026123)
    • (2007) Indian Journal of Pharmaceutical Sciences , vol.69 , Issue.2 , pp. 304-307
    • Alagarsamy, V.1    Murugesan, S.2    Dhanabal, K.3    Murugan, M.4    De Clercq, E.5
  • 58
    • 80054867846 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of newly fused quinazolinone derivatives
    • El- Shareif, A.M.; Micky, J.A.A.; Sharaf, H.F. Synthesis and antimicrobial activity of newly fused quinazolinone derivatives. J. Taibah Univ. Sci., 2008, 1, 51-60.
    • (2008) J. Taibah Univ. Sci. , vol.1 , pp. 51-60
    • El- Shareif, A.M.1    Micky, J.A.A.2    Sharaf, H.F.3
  • 59
    • 70249092581 scopus 로고    scopus 로고
    • Synthesis leading to novel 2,4,6-trisubstituted quinazoline derivatives, their antibacterial and cytotoxic activity against THP-1, HL-60 and A-375 cell lines
    • Chandrika, M.P.; Yakaiah, T.; Narsaiah, B.; Sridhar, V.; Venugopal, G.; Rao, J.V.; Kumar, K.P.; Murthy, U.S.N.; Rao, A.R. Synthesis leading to novel 2,4,6-trisubstituted quinazoline derivatives, their antibacterial and cytotoxic activity against THP-1, HL-60 and A-375 cell lines. Indian J. Chem., 2009, 48B, 840-847.
    • (2009) Indian J. Chem. , vol.48 B , pp. 840-847
    • Chandrika, M.P.1    Yakaiah, T.2    Narsaiah, B.3    Sridhar, V.4    Venugopal, G.5    Rao, J.V.6    Kumar, K.P.7    Murthy, U.S.N.8    Rao, A.R.9
  • 60
    • 41149120622 scopus 로고    scopus 로고
    • Antimicrobial study of newly synthesized lanthanide(III) complexes of 2-[2-hydroxy-3-methoxyphenyl]-3-[2-hydroxy-3-methoxybenzylamino]-1, 2-dihydroquinazolin-4(3H)-one
    • DOI 10.1155/2007/37348, PII S0793029107373485
    • Gudasi, K.B.; Havanur, V.C.; Patil, S.A, Patil, B.R. Antimicrobial study of newly synthesized lanthanide (III) complexes of 2-[2-hydroxy-3- methoxyphenyl]-3-[2-hydroxy-3-methoxybenzylamino]-1,2- dihydroquinazolin-4(3H)- one. Metal-Based Drugs, 2007, 2007:37348 doi: 10.1155/2007/37348. (Pubitemid 351441740)
    • (2007) Metal-Based Drugs , vol.2007 , pp. 37348
    • Gudasi, K.B.1    Havanur, V.C.2    Patil, S.A.3    Patil, B.R.4
  • 61
    • 19944393889 scopus 로고    scopus 로고
    • Niementowski reaction: Microwave induced and conventional synthesis of quinazolinones and 3-methyl-1H-5-pyrazolones and their antimicrobial activity
    • General Papers
    • Desai, R.; Desai, A.; Kishore, R. Niementowski reaction: Microwave induced and conventional synthesis of quinazolinones and 3-methyl-1H-5- pyrazolones and their antimicrobial activity. ARKIVOC, 2005, 8, 98-108. (Pubitemid 40757042)
    • (2005) Arkivoc , vol.2005 , Issue.13 , pp. 98-108
    • Desai, A.R.1    Desai, K.R.2
  • 62
    • 33846277191 scopus 로고    scopus 로고
    • Synthesis and studies of the biological activity of novel pyrimido fused acridine derivatives
    • Patel, B.B.; Patel, R.G.; Patel, M.P. Synthesis and studies of the biological activity of novel pyrimido fused acridine derivatives. J. Serb. Chem. Soc., 2006, 71(10), 1015-1023.
    • (2006) J. Serb. Chem. Soc. , vol.71 , Issue.10 , pp. 1015-1023
    • Patel, B.B.1    Patel, R.G.2    Patel, M.P.3
  • 63
    • 80054859711 scopus 로고    scopus 로고
    • Novel 4(3H)-quinazolinone containing biologically active thiazole, pyrazole, 1,3-dithiazole, pyridine, chromene, pyrazolopyrimidine and pyranochromene of Expected Biological Activity
    • Khairy, A.M.; El-Bayouki, Aly, M.M, Mohamed, Y.A.; Basyouni, W.M.; Abbas, Y.S. Novel 4(3H)-quinazolinone containing biologically active thiazole, pyrazole, 1,3-dithiazole, pyridine, chromene, pyrazolopyrimidine and pyranochromene of Expected Biological Activity. World J. Chem., 2009, 4(2), 161-170.
    • (2009) World J. Chem. , vol.4 , Issue.2 , pp. 161-170
    • Khairy, A.M.1    El-Bayouki Aly, M.M.2    Mohamed, Y.A.3    Basyouni, W.M.4    Abbas, Y.S.5
  • 65
    • 80054858484 scopus 로고    scopus 로고
    • New quinazoline related derivatives with antimicrobial activity: Part-1
    • Mosaad, S.M.; Mohammed, K.I.; Ahmed, M.A.; Abdel-Hamide, S.G. New quinazoline related derivatives with antimicrobial activity: Part-1. Pak. J. Biol. Sci., 2004, 7(7), 1262-1268.
    • (2004) Pak. J. Biol. Sci. , vol.7 , Issue.7 , pp. 1262-1268
    • Mosaad, S.M.1    Mohammed, K.I.2    Ahmed, M.A.3    Abdel-Hamide, S.G.4
  • 66
    • 62749192547 scopus 로고    scopus 로고
    • Synthesis and anti-microbial screening of some schiff bases of 3-amino-6,8-dibromo-2- phenylquinazolin-4(3H)-ones
    • Panneerselvam, P.; Rather, B.A.; Reddy, D.R.S.; Kumar, N.R. Synthesis and anti-microbial screening of some schiff bases of 3-amino-6,8-dibromo-2- phenylquinazolin-4(3H)-ones. Eur. J. Med. Chem., 2009, 44, 2328-2333.
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 2328-2333
    • Panneerselvam, P.1    Rather, B.A.2    Reddy, D.R.S.3    Kumar, N.R.4
  • 67
    • 60549100157 scopus 로고    scopus 로고
    • Nizzamudin Antimicrobial studies of some novel quinazolinones fused with [ 1,2,4]-triazole, [1 24]-triazine and [1,2,4,5]-tetrazine rings
    • Pandey, S.K.; Singh, A.; Singh, A.; Nizzamudin. Antimicrobial studies of some novel quinazolinones fused with [1,2,4]-triazole, [1,2,4]-triazine and [1,2,4,5]-tetrazine rings. Eur. J. Med. Chem., 2009, 44, 1188-1197.
    • (2009) Eur. J. Med. Chem. , vol.44 , pp. 1188-1197
    • Pandey, S.K.1    Singh, A.2    Singh, A.3
  • 68
    • 38149003016 scopus 로고    scopus 로고
    • Synthesis and antimicrobial activity of 3,4-dihydroquinazolinone, quinoxaline, benzoxazine, benzothiazine, pyran and pyrrolidinedione derivatives
    • Fawzy, N.M.; Swelem, S.A.; Farid, M.A. Synthesis and antimicrobial activity of 3,4-dihydroquinazolinone, quinoxaline, benzoxazine, benzothiazine, pyran and pyrrolidinedione derivatives. Biotechnology, 2008, 7(1), 43-50.
    • (2008) Biotechnology , vol.7 , Issue.1 , pp. 43-50
    • Fawzy, N.M.1    Swelem, S.A.2    Farid, M.A.3
  • 69
    • 85038517406 scopus 로고    scopus 로고
    • Synthesis and antimicrobial evaluation of new (4-oxo-thiazolidinyl) quinazolin-4(3H)ones of 2-[(2,6-dichlorophenyl)amino]phenylacetic acid
    • Patel, N.B.; Patel, V.N. Synthesis and antimicrobial evaluation of new (4- oxo-thiazolidinyl)-quinazolin-4(3H)-ones of 2-[(2,6-dichlorophenyl)amino]- phenylacetic acid. Iran. J. Pharm. Res., 2007, 6(4), 251-258. (Pubitemid 351338513)
    • (2007) Iranian Journal of Pharmaceutical Research , vol.6 , Issue.4 , pp. 251-258
    • Patel, N.B.1    Patel, V.N.2
  • 70
    • 33846301981 scopus 로고    scopus 로고
    • Synthesis antibacterial and antifungal activity of some new pyrido quinazolones
    • Singh, V.K.; Pandey, V.K. Synthesis, antibacterial and antifungal activity of some new pyrido quinazolones. Indian J. Chem., 2006, 45B, 2745-2748.
    • (2006) Indian J. Chem. , vol.45 B , pp. 2745-2748
    • Singh, V.K.1    Pandey, V.K.2
  • 71
    • 80054875657 scopus 로고    scopus 로고
    • Choices of drugs for self treatment of malaria among adult women in a Nigerian city: Implications for the success of the ongoing 'roll back' malaria programme
    • Jombo, G.T.A.; Denen, Akaa, P.; Alao, O.O.; Peters, E.J.; Dauda, M.A.; Okwari, E.E.; Akosu, T.J.; Etu, Kumana, E.A.; Yaakugh, J.B. Choices of drugs for self treatment of malaria among adult women in a Nigerian city: Implications for the success of the ongoing 'roll back' malaria programme. J. Microbiol. Antimicrob., 2010, 2(6), 57-63.
    • (2010) J. Microbiol. Antimicrob. , vol.2 , Issue.6 , pp. 57-63
    • Jombo, G.T.A.1    Denen Akaa, P.2    Alao, O.O.3    Peters, E.J.4    Dauda, M.A.5    Okwari, E.E.6    Akosu, T.J.7    Etu Kumana, E.A.8    Yaakugh, J.B.9
  • 72
    • 0036682237 scopus 로고    scopus 로고
    • Synthesis and in vitro studies of novel pyrimidinyl peptidomimetics as potential antimalarial therapeutic agents
    • Zhu, S.; Hudson, T.H.; Kyle, D.E.; Lin, A.J. Synthesis and in vitro studies of novel pyrimidinyl peptidomimetics as potential antimalarial therapeutic agents. J. Med. Chem., 2002, 45(16), 3491.
    • (2002) J. Med. Chem. , vol.45 , Issue.16 , pp. 3491
    • Zhu, S.1    Hudson, T.H.2    Kyle, D.E.3    Lin, A.J.4
  • 73
    • 0000479718 scopus 로고
    • An alkaloid with high anti malarial activity from Dichroa febrifuga
    • Koepfli, J.B.; Mead, J.F.; Brockman, J.A. An alkaloid with high anti malarial activity from Dichroa febrifuga. J. Am. Chem. Soc., 1947, 69, 1837.
    • (1947) J. Am. Chem. Soc. , vol.69 , pp. 1837
    • Koepfli, J.B.1    Mead, J.F.2    Brockman, J.A.3
  • 74
    • 33947447542 scopus 로고
    • Alkaloids of Dichroa febrifuga. I. Isolation and degradative studies
    • Koepfli, J.B.; Mead, J.F.; Brockman, J.A. Alkaloids of Dichroa febrifuga. I. Isolation and degradative studies. J. Am. Chem. Soc.,1949, 71, 1048-1054.
    • (1949) J. Am. Chem. Soc. , vol.71 , pp. 1048-1054
    • Koepfli, J.B.1    Mead, J.F.2    Brockman, J.A.3
  • 75
    • 0014850623 scopus 로고
    • Structural modifications of febrifugine: Some methylenedioxy analogs
    • Chien, P.L; Cheng, C.C. Structural modifications of febrifugine: Some methylenedioxy analogs. J. Med. Chem., 1970, 13(5), 867-870.
    • (1970) J. Med. Chem. , vol.13 , Issue.5 , pp. 867-870
    • Chien, P.L.1    Cheng, C.C.2
  • 77
    • 80054852022 scopus 로고    scopus 로고
    • Chemotherapeutic agents targeting tuberculosis
    • S.R. Garg., A. Kumar and Y. Singh (Editors), CCS Haryana Agricultural University, Hisar
    • Mishra, D.N.; Sharma, P.C.; Jain, S. Chemotherapeutic agents targeting tuberculosis. Interdisciplinary Approach for Tuberculosis Control, S.R. Garg., A. Kumar and Y. Singh (Editors), CCS Haryana Agricultural University, Hisar, 2007, 70-77.
    • (2007) Interdisciplinary Approach for Tuberculosis Control , pp. 70-77
    • Mishra, D.N.1    Sharma, P.C.2    Jain, S.3
  • 78
    • 10444227369 scopus 로고    scopus 로고
    • Fighting tuberculosis: An old disease with new challenges
    • Tripathi, R.P.; Tewari, N.; Dwivedi, N.; Tiwari, V.K. Fighting tuberculosis: An old disease with new challenges. Med. Res. Rev., 2005, 25, 131(1-75)
    • (2005) Med. Res. Rev. , vol.25 , Issue.1-75 , pp. 131
    • Tripathi, R.P.1    Tewari, N.2    Dwivedi, N.3    Tiwari, V.K.4
  • 79
    • 0011523808 scopus 로고    scopus 로고
    • Global tuberculosis control
    • World Health Organisation
    • World Health Organisation. Global Tuberculosis Control; WHO Report 2001;
    • (2001) WHO Report
  • 80
    • 80054865843 scopus 로고    scopus 로고
    • World Health Organisation: Geneva, Switzerland; WHO/CDS/TB/2001.287
    • World Health Organisation: Geneva, Switzerland; WHO/CDS/TB/2001.287.
  • 81
    • 84862760354 scopus 로고    scopus 로고
    • World Health Organisation Tuberculosis Fact Sheet, No. 104
    • World Health Organisation Tuberculosis Fact Sheet, No. 104, 2000; http://www.who.int/inf-fs/en/fact104.html.
    • (2000)
  • 82
    • 15844392910 scopus 로고    scopus 로고
    • World Health Organisation issues another gloomy tuberculosis report
    • Mooran, N. World Health Organisation issues another gloomy tuberculosis report, Nature Medicine, 1996, 2, 377.
    • (1996) Nature Medicine , vol.2 , pp. 377
    • Mooran, N.1
  • 84
    • 0033581124 scopus 로고    scopus 로고
    • Global burden of tuberculosis: E stimated incidence, prevalence, and mortality by country. WHO Global Surveillance and Monitoring Project
    • Dye, C.; Scheele, S.; Dolin, P,; Pathania, V.; Raviglione, M.C. Global burden of tuberculosis: E stimated incidence, prevalence, and mortality by country. WHO Global Surveillance and Monitoring Project. J. Am. Med Assoc., 1999, 282, 677-686.
    • (1999) J. Am. Med Assoc. , vol.282 , pp. 677-686
    • Dye, C.1    Scheele, S.2    Dolin, P.3    Pathania, V.4    Raviglione, M.C.5
  • 87
    • 79953244748 scopus 로고    scopus 로고
    • Synthesis of some new 3H-quinazolin-4-one derivatives as potential antitubercular agents
    • Al-deeb, A.O.; Alafeefy, A.M. Synthesis of some new 3H-quinazolin-4-one derivatives as potential antitubercular agents. World Applied Sciences Journal, 2008, 5(1), 94-99.
    • (2008) World Applied Sciences Journal , vol.5 , Issue.1 , pp. 94-99
    • Al-deeb, A.O.1    Alafeefy, A.M.2
  • 88
    • 33750066952 scopus 로고    scopus 로고
    • Antituberculosis drugs and hepatotoxicity
    • DOI 10.1111/j.1440-1843.2006.00941.x
    • Yew, W.W.; Leung, C.C. Antituberculosis drugs and hepatotoxicity. Respirology, 2003, 11, 699-707. (Pubitemid 44581433)
    • (2006) Respirology , vol.11 , Issue.6 , pp. 699-707
    • Yew, W.W.1    Leung, C.C.2
  • 89
    • 33846073563 scopus 로고    scopus 로고
    • New derivatives of BM212: A class of antimycobacterial compounds based on the pyrrole ring as a scaffold
    • DOI 10.2174/138955707779317786
    • Biava, M.; Porretta, A.; Manetti, F. A class of antimycobacterial compounds based on the pyrrole ring as a scaffold. Mini. Rev. Med. Chem., 2007, 7, 65-78. (Pubitemid 46062375)
    • (2007) Mini-Reviews in Medicinal Chemistry , vol.7 , Issue.1 , pp. 65-78
    • Biava, M.1    Porretta, G.C.2    Manetti, F.3
  • 90
    • 0029119954 scopus 로고
    • Synthesis and antimicrobial evaluation of new quinazolinone derivatives
    • Guersoy, A.; Illhan, N. Synthesis and antimicrobial evaluation of new quinazolinone derivatives. Il Farmaco, 1995, 50, 559-562.
    • (1995) Il Farmaco , vol.50 , pp. 559-562
    • Guersoy, A.1    Illhan, N.2
  • 91
    • 0033395476 scopus 로고    scopus 로고
    • Synthesis, antibacterial, antifungal and anti-HIV evaluation of Schiff and Mannich bases of isatin derivatives with 3-amino-2-methylmercapto quinazolin-4(3H)-one
    • DOI 10.1016/S0031-6865(99)00010-2, PII S0031686599000102
    • Pandeya, S.N.; Sriram, D.; Nath, G.; Clerke, E.De. Synthesis, antibacterial, antifungal and anti HIV evaluation of Schiff and mannich bases of isatin derivatives with 3-amino-2-methylmercaptoquinazolin-4(3H)-one. Pharm. Acta. Helv.,1999, 74, 11-17. (Pubitemid 30035398)
    • (1999) Pharmaceutica Acta Helvetiae , vol.74 , Issue.1 , pp. 11-17
    • Pandeya, S.N.1    Sriram, D.2    Nath, G.3    De Clercq, E.4
  • 92
    • 33644944329 scopus 로고    scopus 로고
    • Synthesis and evaluation of new quinazolone derivatives of nalidixic acid as potential antibacterial and antifungal agents
    • Grover, G.; Kini, S.G. Synthesis and evaluation of new quinazolone derivatives of nalidixic acid as potential antibacterial and antifungal agents. Eur. J. Med. Chem., 2006, 41, 256-262.
    • (2006) Eur. J. Med. Chem. , vol.41 , pp. 256-262
    • Grover, G.1    Kini, S.G.2
  • 93
    • 0034525276 scopus 로고    scopus 로고
    • Quinazoline derivatives with antitubercular activity
    • DOI 10.1016/S0014-827X(00)00100-2, PII S0014827X00001002
    • Kunes, J.; Bazant, J.; Pour, M.; Waisser, K.; Slosarek, M.; Janota, J. Quinazoline derivatives with antitubercular activity. Il Farmaco, 2000, 55, 725-729. (Pubitemid 32037105)
    • (2000) Farmaco , vol.55 , Issue.11-12 , pp. 725-729
    • I Kune, J.1    Jaroslav, B.2    Pour, M.3    Waisser, K.4    Iosarek, M.5    I Janota, J.6
  • 95
    • 0142248975 scopus 로고    scopus 로고
    • 3-Benzyl-2H-1,3-benzoxazine-2,4(3H)-diones, a new group of antimycobacterial compounds against potentially pathogenic strains
    • DOI 10.1016/j.farmac.2003.07.004
    • Waisser, K.; Perina, M.; Kunes, J.; Klimesova, V.; Kaustova, J. 3-Benzyl- 2H-1,3-benzoxazine- 2,4(3H)-diones, a new group of antimycobacterial compounds against potentially pathogenic strains. Il Farmaco, 2003, 58, 1137-1149. (Pubitemid 37323933)
    • (2003) Farmaco , vol.58 , Issue.11 , pp. 1137-1149
    • Waisser, K.1    Perina, M.2    Kunes, J.3    Klimesova, V.4    Kaustova, J.5
  • 96
    • 34250698412 scopus 로고    scopus 로고
    • The oriented development of antituberculotics (Part II): Halogenated 3-(4-alkylphenyl)-1,3-benzoxazine-2,4-(3H)-diones
    • DOI 10.1002/ardp.200600002
    • Waisser, K.; Matyk, J.; Divisova, H.; Husakova, P.; Kunes, J.; Klimesova, V.; Palat, K.; Kaustova, J. The oriented development of antituberculotics (Part II): Halogenated 3-(4-Alkylphenyl)-1,3- benzoxazine-2,4-(3H)-diones. Arch. Pharm. (weinheim), 2007, 340(5), 264-267. (Pubitemid 46959729)
    • (2007) Archiv der Pharmazie , vol.340 , Issue.5 , pp. 264-267
    • Waisser, K.1    Matyk, J.2    Divisova, H.3    Husakova, P.4    Kunes, J.5    Klimesova, V.6    Palat, K.7    Kaustova, J.8
  • 98
    • 0020596551 scopus 로고
    • Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS)
    • Barre-Sinoussi, F.; Chermann, J.C.; Rey, F.; Nugeyre, M.T.; Chamaret, S.; Gruest, J. Isolation of a T-lymphotropic retrovirus from a patient at risk for acquired immune deficiency syndrome (AIDS). Science, 1983, 220, 868-71. (Pubitemid 13080157)
    • (1983) Science , vol.220 , Issue.4599 , pp. 868-871
    • Barre Sinoussi, F.1    Chermann, J.C.2    Rey, F.3
  • 99
    • 0021261510 scopus 로고
    • Frequent detection and isolation of cytopathic retroviruses (HTLV-III) from patients with AIDS and at risk for AIDS
    • Gallo, R.C.; Salahuddin, S.Z.; Popovic, M.; Shearer, G.M.; Kaplan, M.; Haynes, B.F. Frequent detection and isolation of cytopathic retroviruses (HTLV-III) from patients with AIDS and at risk for AIDS. Science 1984, 224, 500-503. (Pubitemid 14134741)
    • (1984) Science , vol.224 , Issue.4648 , pp. 500-503
    • Gallo, R.C.1    Salahuddin, S.Z.2    Popovic, M.3
  • 100
    • 78650845766 scopus 로고    scopus 로고
    • Simple and rapid RPHPLC method for chromatographic purity of anti-retroviral drug lamivudine
    • Kakkar, S.; Mohanraj, K.; Aakashdeep.; Sharma, P.C. Simple and rapid RPHPLC method for chromatographic purity of anti-retroviral drug lamivudine. Lat. Am. J. Pharm., 2010, 29(7), 1075-1081.
    • (2010) Lat. Am. J. Pharm , vol.29 , Issue.7 , pp. 1075-1081
    • Kakkar, S.1    Mohanraj, K.2    Aakashdeep3    Sharma, P.C.4
  • 101
    • 12144265244 scopus 로고    scopus 로고
    • Non- nucleoside reverse transcriptase inhibitors (NNRTIs): Past, present and future
    • De Clercq, E. Non- nucleoside reverse transcriptase inhibitors (NNRTIs): Past, present and future. Chem. Biodiversity, 2004, 1, 44-64.
    • (2004) Chem. Biodiversity , vol.1 , pp. 44-64
    • De Clercq, E.1
  • 103
    • 80054866445 scopus 로고    scopus 로고
    • In: Bioinformatics in pharma research
    • Narosa publishing house New Delhi, India
    • Singla, S.; Kumar, H.; Sharma, P.C. In: Bioinformatics in pharma research. In bioinformatics computing. Narosa publishing house, 2007, New Delhi, India, pp. 131-138.
    • (2007) Bioinformatics Computing , pp. 131-138
    • Singla, S.1    Kumar, H.2    Sharma, P.C.3
  • 104
    • 4043145820 scopus 로고    scopus 로고
    • Obstacles to successful antiretroviral treatment of HIV-1 infection: Problems and perspectives
    • Potter, S.J.; Chew. C.B.; Steain, M.; Dwyer, D.E.; Saksena, N.K. Obstacles to successful antiretroviral treatment of HIV-1 infection: Problems & perspectives. Indian J. Med. Res., 2004, 119, 217-237. (Pubitemid 39076952)
    • (2004) Indian Journal of Medical Research , vol.119 , Issue.6 , pp. 217-237
    • Potter, S.J.1    Chew, C.B.2    Steain, M.3    Dwyer, D.E.4    Saksena, N.K.5
  • 105
    • 80054875469 scopus 로고    scopus 로고
    • Synthesis anti-viral and cytotoxic studies of some 2-phenyl-3-substituted quinazolin-4-(3H)-ones
    • Yuvraj, G.; Meena, A.; Dillibabu.; Kumar, G.S.; Arvind, M.; Kumar, N.R. Synthesis, anti-viral and cytotoxic studies of some 2-phenyl-3-substituted quinazolin-4-(3H)-ones. Int. J. Pharm. Res., 2009, 1(3), 141-145.
    • (2009) Int. J. Pharm. Res. , vol.1 , Issue.3 , pp. 141-145
    • Yuvraj, G.1    Meena, A.2    Dillibabu3    Kumar, G.S.4    Arvind, M.5    Kumar, N.R.6
  • 106
    • 38149104561 scopus 로고    scopus 로고
    • Synthesis and antiviral bioactivities of 2-aryl- or 2-methyl-3- (substituted-benzalamino)- 4(3H)-quinazolinone derivatives
    • Gao, X.; Cai, X.; Yan, K.; Song, B.; Gao, L.; Chen, Z. Synthesis and antiviral bioactivities of 2-aryl- or 2-methyl-3-(substituted-benzalamino)- 4(3H)-quinazolinone derivatives. Molecules, 2007, 12, 2621-2642.
    • (2007) Molecules , vol.12 , pp. 2621-2642
    • Gao, X.1    Cai, X.2    Yan, K.3    Song, B.4    Gao, L.5    Chen, Z.6
  • 108
    • 0036202836 scopus 로고    scopus 로고
    • The promise of new antiepileptic drugs
    • DOI 10.1046/j.0306-5251.2001.01540.x
    • Duncan, J.S. The promise of new antiepileptic drugs. Br. J. Clin. Pharmacol., 2002, 53, 123-131. (Pubitemid 34264266)
    • (2002) British Journal of Clinical Pharmacology , vol.53 , Issue.2 , pp. 123-131
    • Duncan, J.S.1
  • 109
    • 1342300726 scopus 로고    scopus 로고
    • Synthesis of some newer derivatives of substituted quinazolinonyl-2-oxo/ thiobarbituric acid as potent anticonvulsant agents
    • DOI 10.1016/j.bmc.2003.08.035
    • Archana.; Srivastava, V.K.; Kumar, A. Synthesis of some newer derivatives of substituted quinazolinonyl-2-oxo/thiobarbituric acid as potent anticonvulsant agents. Bioorg. Med. Chem., 2004, 12, 1257-1264. (Pubitemid 38251316)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.5 , pp. 1257-1264
    • Archana1    Srivastava, V.K.2    Kumar, A.3
  • 110
    • 1842858323 scopus 로고    scopus 로고
    • Synthesis of newer thiadiazolyl and thiazolidinonyl quinazolin-4(3H)-ones as potential anticonvulsant agents
    • DOI 10.1016/S0223-5234(02)01389-2, PII S0223523402013892
    • Srivastava, A.V.K.; Kumar, A. Synthesis of newer thiadiazolyl and thiazolidinonyl quinazolin-4(3H)-ones as potential anticonvulsant agents. Eur. J. Med. Chem., 2002, 37, 873-882. (Pubitemid 35356423)
    • (2002) European Journal of Medicinal Chemistry , vol.37 , Issue.11 , pp. 873-882
    • Archana1    Srivastava, V.K.2    Kumar, A.3
  • 111
    • 0038166026 scopus 로고    scopus 로고
    • Design and synthesis of some new derivatives of 3H-quinazolin-4-one with promising anticonvulsant activity
    • Helby, A.G.; Hameda, M.; Wahab, A. Design and synthesis of some new derivatives of 3H-quinazolin-4-one with promising anticonvulsant activity. Acta Pharm., 2003, 53, 127-138. (Pubitemid 36850884)
    • (2003) Acta Pharmaceutica , vol.53 , Issue.2 , pp. 127-138
    • El-Helby, A.G.A.1    Wahab, M.H.A.2
  • 112
    • 0025157161 scopus 로고
    • Synthesis and anticonvulsant activity of some new 2-substituted 3-aryl-4(3H)-quinazolinones
    • DOI 10.1021/jm00163a027
    • Wolfe, J.F.; Rathman, T.L.; Sleevi, M.C.; Campbell, J.A.; Greenwood, T.D. Synthesis and anticonvulsant activity of some new 2-substituted-3-aryl-(3H)- quinazolinones. J. Med. Chem., 1990, 33(1),161-166. (Pubitemid 20038187)
    • (1990) Journal of Medicinal Chemistry , vol.33 , Issue.1 , pp. 161-166
    • Wolfe, J.F.1    Rathman, T.L.2    Sleevi, M.C.3    Campbell, J.A.4    Greenwood, T.D.5
  • 113
    • 4644337416 scopus 로고    scopus 로고
    • Synthesis and anticonvulsant evaluation of some new 2-substituted-3- arylpyrido[2,3-d]pyrimidinones
    • DOI 10.1016/j.bmc.2004.07.068, PII S0968089604005413
    • White, D.C.; Greenwood, T.D.; Downey, A.L.; Bloomquist, A.R.; Wolfe, J.F. Synthesis and anticonvulsant evaluation of some new 2-substituted-3- arylpyrido[2,3-d]pyrimidinones. Bioorg. Med. Chem., 2004, 12, 5711-5717. (Pubitemid 39304068)
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , Issue.21 , pp. 5711-5717
    • White, D.C.1    Greenwood, T.D.2    Downey, A.L.3    Bloomquist, J.R.4    Wolfe, J.F.5
  • 114
    • 0041733096 scopus 로고    scopus 로고
    • Improved reversal learning and altered fear conditioning in transgenic mice with regionally restricted p25 expression
    • DOI 10.1046/j.1460-9568.2003.02746.x
    • Angelo,. M.; Plattner, F.; Irvine, E.E.; Giese, K.P. Improved reversal learning altered fear conditioning in transgenic mice with regionally restricted p25 expression. Eur. J. Neurosci., 2003, 18(2), 423-431. (Pubitemid 36999943)
    • (2003) European Journal of Neuroscience , vol.18 , Issue.2 , pp. 423-431
    • Angelo, M.1    Plattner, F.2    Irvine, E.E.3    Giese, K.P.4
  • 115
    • 13944249205 scopus 로고    scopus 로고
    • Enhanced CDK5 activity and p35 translocation in the venral striatum of acute and chronic methamphetamine-treated rats
    • Chen, P.C.; Chen, J.C. Enhanced CDK5 activity and p35 translocation in the venral striatum of acute and chronic methamphetamine-treated rats. Neuropsychopharmacol., 2005, 30(3), 538-549.
    • (2005) Neuropsychopharmacol. , vol.30 , Issue.3 , pp. 538-549
    • Chen, P.C.1    Chen, J.C.2
  • 118
    • 0345120702 scopus 로고
    • Synthesis and CNS activity of some 2-Aryl/Alkyl-3-[N-phenyl-N-(dihydroxy- phenyl-methyl)-amino]-6,8- disubstituted quinazolin-4(3H)-ones
    • Tiwari, S.S.; Satsangi R.K.; Agarwal, R. Synthesis and CNS activity of some 2-Aryl/Alkyl-3-[N-phenyl-N-(dihydroxy-phenyl-methyl)-amino]-6,8- disubstituted quinazolin-4(3H)-ones. Curr. Sci., 1979, 48, 568-571.
    • (1979) Curr. Sci. , vol.48 , pp. 568-571
    • Tiwari, S.S.1    Satsangi, R.K.2    Agarwal, R.3
  • 119
    • 33847341849 scopus 로고    scopus 로고
    • Synthesis of some new 4-(3H)-quinazoline analogs as potential antioxidant agents
    • Omar-Al, M.A.; Azab-El Adel, S.; Obeid-El, H.A.; Hamide, S.G. Synthesis of some new 4-(3H)-quinazoline analogs as potential antioxidant agents. J. Saudi Chem. Soc., 2006, 10, 113-130.
    • (2006) J. Saudi Chem. Soc , vol.10 , pp. 113-130
    • Omar-Al, M.A.1    Azab-El Adel, S.2    Obeid-El, H.A.3    Hamide, S.G.4
  • 120
    • 72749102009 scopus 로고    scopus 로고
    • Synthesis, structure activity relationship studies and pharmacological evaluation of 2-phenyl-3-(substituted phenyl)- 3H-quinazolin-4-ones as serotonin 5-HT2 antagonist
    • Sati, N.; Kumar, S.; Rawat, M.S.M. Synthesis, structure activity relationship studies and pharmacological evaluation of 2-phenyl-3-(substituted phenyl)- 3H-quinazolin-4-ones as serotonin 5-HT2 antagonist. Indian J. Pharm. Sci., 2009, 71(5), 572-575.
    • (2009) Indian J. Pharm. Sci. , vol.71 , Issue.5 , pp. 572-575
    • Sati, N.1    Kumar, S.2    Rawat, M.S.M.3
  • 121
    • 50949089653 scopus 로고    scopus 로고
    • CNS depressant and anticonvulsant activities of some novel 3-[5-substituted-1,3,4-thiadiazole-2- yl]-2-styrylquinazoline-4(3H)-ones
    • Jatav, V.; Mishra, P.; Kashaw, S.; Stables, J.P. CNS depressant and anticonvulsant activities of some novel 3-[5-substituted-1,3,4-thiadiazole-2- yl]-2-styrylquinazoline-4(3H)-ones. Eur. J. Med. Chem., 2008, 43, 1945-1954.
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 1945-1954
    • Jatav, V.1    Mishra, P.2    Kashaw, S.3    Stables, J.P.4
  • 122
    • 33748570348 scopus 로고    scopus 로고
    • J.J. Buccafusco (Ed.), Birkhauser Verlag, Basel, Boston, Berlin
    • Giacobini, E; In: Cognitive Enhancing Drugs; J.J. Buccafusco (Ed.), Birkhauser Verlag, Basel, Boston, Berlin, 2004, pp. 11-36.
    • (2004) Cognitive Enhancing Drugs , pp. 11-36
    • Giacobini, E.1
  • 123
    • 0029827996 scopus 로고    scopus 로고
    • Novel anticholinesterase and antiamnesic activities of dehydroevodiamine, a constituent of Evodia rutaecarpa
    • DOI 10.1055/s-2006-957926
    • Park, C.H.; Kim, S.H.; Choi, W.; Lee, Y.L.; Kim, J..S.; Kang, S.S.; Suh, Y.H. Novel anticholinesterase and antiamnesic activities of dihydroevodiamine, a constituent of Evodia rutaecarpa. Planta Med., 1996, 62(5), 405-409. (Pubitemid 26370329)
    • (1996) Planta Medica , vol.62 , Issue.5 , pp. 405-409
    • Park, C.H.1    Kim, S.-H.2    Choi, W.3    Lee, Y.-J.4    Kim, J.S.5    Kang, S.S.6    Suh, Y.H.7
  • 124
    • 13844253966 scopus 로고    scopus 로고
    • Novel inhibitors of acetyl- and butyrylcholinesterase derived from the alkaloids dehydroevodiamine and rutaecarpine
    • DOI 10.1016/j.ejmech.2004.12.003
    • Decker, M. Novel inhibitors of acetyl- and butyrylcholinesterase derived from the alkaloids dehydroevodiamine and rutaecarpine. Eur. J. Med. Chem., 2005, 40, 305-313. (Pubitemid 40255773)
    • (2005) European Journal of Medicinal Chemistry , vol.40 , Issue.3 , pp. 305-313
    • Decker, M.1
  • 125
    • 67749088018 scopus 로고    scopus 로고
    • S and C-nucleoside quinazoline as new nucleoside analogs with potential analgesic and antiinflammatory activity
    • El-Gazzar, B.A.; Hafez, H.N.; Abbas, H.A.S. S- and C-nucleoside quinazoline as new nucleoside analogs with potential analgesic and antiinflammatory activity. Eur. J. Med. Chem., 2009, 44, 4249-4258.
    • (2009) Eur. J. Med. Chem , vol.44 , pp. 4249-4258
    • El-Gazzar, B.A.1    Hafez, H.N.2    Abbas, H.A.S.3
  • 128
    • 0031450208 scopus 로고    scopus 로고
    • Partial loss of tolerance liability to morphine analgesia in mice lacking the nociceptin receptor gene
    • DOI 10.1016/S0304-3940(97)00832-X, PII S030439409700832X
    • Ueda, H.; Yamaguchi, T.; Tokuyama, S.; Inoue, M.; Nishi, M.; Takeshima, H. Partial loss of tolerance liability to morphine analgesia in mice lacking nociceptin receptor gene. Neurosci. Lett., 1997, 237(3), 136-138. (Pubitemid 28004975)
    • (1997) Neuroscience Letters , vol.237 , Issue.2-3 , pp. 136-138
    • Ueda, H.1    Yamaguchi, T.2    Tokuyama, S.3    Inoue, M.4    Nishi, M.5    Takeshima, H.6
  • 129
    • 0030601730 scopus 로고    scopus 로고
    • Orphanin FQ is a functional anti-opioid peptide
    • DOI 10.1016/0306-4522(96)00338-7, PII S0306452296003387
    • Mogil, J.S.; Grisel, JE.; Reinscheid, R.K.; Civelli, O.; Belknap, J.K.; Grandy, D.K. Orphanin FQ is a functional anti opoid peptide. Neuroscience, 1996, 75(2), 333-337. (Pubitemid 26361325)
    • (1996) Neuroscience , vol.75 , Issue.2 , pp. 333-337
    • Mogil, J.S.1    Grisel, J.E.2    Reinscheid, R.K.3    Civelli, O.4    Belknap, J.K.5    Grandy, D.K.6
  • 131
    • 0030581735 scopus 로고    scopus 로고
    • Nociceptin stimulates locomotion and exploratory behaviour in mice
    • DOI 10.1016/S0014-2999(96)00707-8, PII S0014299996007078
    • Florin, S.; Suaudeau, C.; Meunier, J.C.; Costentin, J. Nociceptin stimulates locomotion and exploratory behavior in mice. Eur. J. Pharmacol., 1996, 317(1), 9-13. (Pubitemid 26427007)
    • (1996) European Journal of Pharmacology , vol.317 , Issue.1 , pp. 9-13
    • Florin, S.1    Suaudeau, C.2    Meunier, J.-C.3    Costentin, J.4
  • 132
    • 57649183705 scopus 로고    scopus 로고
    • Discovery and structure-activity relationships of 4-aminoquinazoline derivatives, a novel class of opioid receptor like-1 (ORL1) antagonists
    • Okano, M.; Mito, J.; Maruyama, Y.; Masuda H.; Niwa, T.; Nakagawa, S.I.; Nakamura, Y.; Matsuura, A. Discovery and structure-activity relationships of 4-aminoquinazoline derivatives, a novel class of opioid receptor like-1 (ORL1) antagonists. Bioorg. Med. Chem., 2009, 17, 119-132.
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 119-132
    • Okano, M.1    Mito, J.2    Maruyama, Y.3    Masuda, H.4    Niwa, T.5    Nakagawa, S.I.6    Nakamura, Y.7    Matsuura, A.8
  • 133
    • 41149163183 scopus 로고    scopus 로고
    • Parkinson's disease: Clinical features and diagonosis
    • Jankovic, J.J. Parkinson's disease: Clinical features and diagonosis. Neurol. Neurosurg. Psychiatry, 2008, 79, 368-376.
    • (2008) Neurol. Neurosurg. Psychiatry , vol.79 , pp. 368-376
    • Jankovic, J.J.1
  • 135
    • 0027141494 scopus 로고
    • Cyclic GMP phosphodiesterase inhibitors. 1. The discovery of a novel potent inhibitor, 4-((3,4-(methylenedioxy)benzyl)amino)-6,7,8- trimethoxyquinazoline
    • DOI 10.1021/jm00076a003
    • Takase, Y.; Saeki, T.; Fujimoto, M.; Saito, I. Cyclic GMP phosphodiesterase inhibitors.1. The discovery of a novel potent inhibitor, 4-((3,4- methylenedioxy)benzyl)amino)-6,7,8-trimethoxyquinazoline. J. Med. Chem., 1993, 36(24), 3765-3770. (Pubitemid 24006704)
    • (1993) Journal of Medicinal Chemistry , vol.36 , Issue.24 , pp. 3765-3770
    • Takase, Y.1    Saeki, T.2    Fujimoto, M.3    Saito, I.4
  • 136
    • 67349108013 scopus 로고    scopus 로고
    • CAMP dependent phosphodiesterase inhibition and SAR studies on novel 6,8-disubstituted-2- phenyl-3-(substituted benzothiazo-2-yl)-4(3H)-quinazolinone
    • Laddha, S.S.; Wadodkar, S.G.; Mehgal, S.K. cAMP dependent phosphodiesterase inhibition and SAR studies on novel 6,8-disubstituted-2- phenyl-3-(substituted benzothiazo-2-yl)-4(3H)-quinazolinone. Med. Chem. Res., 2009, 18(4), 268-276.
    • (2009) Med. Chem. Res. , vol.18 , Issue.4 , pp. 268-276
    • Laddha, S.S.1    Wadodkar, S.G.2    Mehgal, S.K.3
  • 137
    • 0028038279 scopus 로고
    • Cyclic GMP phosphodiesterase inhibitors. 2. Requirement of 6-substitution of quinazoline derivatives for potent and selective inhibitory activity
    • DOI 10.1021/jm00039a024
    • Takase, Y.; Saeki, T.; Watanabe, N.; Adachi, N.; Souda, S.; Saito, I. Cyclic GMP phosphodiesterase inhibitors. 2. Requirement of 6-substitution of quinazoline derivatives for potent and selective inhibitory activity. J. Med. Chem., 1994, 37(13), 2106-2111. (Pubitemid 24233624)
    • (1994) Journal of Medicinal Chemistry , vol.37 , Issue.13 , pp. 2106-2111
    • Takase, Y.1    Saeki, T.2    Watanabe, N.3    Adachi, H.4    Souda, S.5    Saito, I.6
  • 140
    • 80054847529 scopus 로고    scopus 로고
    • Synthesis characterization and biological activity of various substituted quinazolinone derivatives containing dopamine moiety
    • Kumar, S.; Kaur, H.; Singh, I.; Sharma, M.; Vishwakarma, P.; Saxena, K.K.; Kumar, A. Synthesis, characterization and biological activity of various substituted quinazolinone derivatives containing dopamine moiety. World J. Chem., 2009, 4(2), 195-200.
    • (2009) World J. Chem. , vol.4 , Issue.2 , pp. 195-200
    • Kumar, S.1    Kaur, H.2    Singh, I.3    Sharma, M.4    Vishwakarma, P.5    Saxena, K.K.6    Kumar, A.7
  • 141
    • 33846975147 scopus 로고    scopus 로고
    • Role of phosphodiesterases in neurological and psychiatric disease
    • DOI 10.1016/j.coph.2006.08.014, PII S1471489206001950, Neurosciences
    • Hebb, A.L.; Robertson, H.A. Role of phosphodiesterase in neurological and psychiatric disease. Curr. Opin. Pharmacol., 2007, 7(1), 86-92. (Pubitemid 46242039)
    • (2007) Current Opinion in Pharmacology , vol.7 , Issue.1 , pp. 86-92
    • Hebb, A.L.1    Robertson, H.A.2
  • 142
    • 27344449614 scopus 로고    scopus 로고
    • Keynote review: Phosphodiesterase-4 as a therapeutic target
    • DOI 10.1016/S1359-6446(05)03622-6, PII S1359644605036226
    • Houslay, M.D.; Schafer, P.; Zhang, K.Y. Keynote review: Phosphodiesterase-4 as a therapeutic target. Drug Discovery Today, 2005, 10, 1503-1519. (Pubitemid 41527193)
    • (2005) Drug Discovery Today , vol.10 , Issue.22 , pp. 1503-1519
    • Houslay, M.D.1    Schafer, P.2    Zhang, K.Y.J.3
  • 143
    • 34247105883 scopus 로고    scopus 로고
    • cAMP-specific phosphodiesterase-4 enzymes in the cardiovascular system: A molecular toolbox for generating compartmentalized cAMP signaling
    • DOI 10.1161/01.RES.0000261934.56938.38, PII 0000301220070413000007
    • Houslay M.D., Baillie, G.S., Maurice, D.H. cAMP specific phosphodiesterase-4 enzymes in the cardiovascular system: A molecular toolbox for generating compartmentalized cAMP signaling. Circ. Res., 2007, 100(7), 950-966. (Pubitemid 46598920)
    • (2007) Circulation Research , vol.100 , Issue.7 , pp. 950-966
    • Houslay, M.D.1    Baillie, G.S.2    Maurice, D.H.3
  • 144
    • 69949169680 scopus 로고    scopus 로고
    • A new therapeutic approach in Parkinson's disease: Some novel quinazoline derivatives as dual selective phosphodiesterase 1 inhibitors and anti-inflammatory agents
    • Laddha, S.S.; Bhatnagar, S.P. A new therapeutic approach in Parkinson's disease: Some novel quinazoline derivatives as dual selective phosphodiesterase 1 inhibitors and anti-inflammatory agents. Bioorg. Med. Chem., 2009, 17, 6796-6802.
    • (2009) Bioorg. Med. Chem. , vol.17 , pp. 6796-6802
    • Laddha, S.S.1    Bhatnagar, S.P.2
  • 145
    • 0026613991 scopus 로고
    • Developments in antihistaminics (H1)
    • Ernst Jucker, Basel
    • Saxena, A.K.; Saxena, M. Developments in antihistaminics (H1), In: Progress in Drug Research, Ernst Jucker, Basel, 1992, pp. 35-126.
    • (1992) Progress in Drug Research , pp. 35-126
    • Saxena, A.K.1    Saxena, M.2
  • 146
    • 0001796572 scopus 로고
    • Histamine Bradykinine. 5-Hydroxytryptamine and their antagonists
    • in: Gilman, A.G.; Rall, T.E.; Nies, A.S.; Taylor, P. (Eds. 8th ed. Pergamon Press, New York
    • Garrison, J.C. Histamine, Bradykinine, 5-Hydroxytryptamine and their antagonists, in: Gilman, A.G.; Rall, T.E.; Nies, A.S.; Taylor, P. (Eds.), The Pharmacological Basis of Therapeutics, 8th ed., Pergamon Press, New York, 1990, pp. 575.
    • (1990) The Pharmacological Basis of Therapeutics , pp. 575
    • Garrison, J.C.1
  • 148
    • 0022382564 scopus 로고
    • Computer-assisted analysis of bioactivity. I. Active conformation of histamine H1 receptor antagonists
    • Naruto, S.; Motoc, I.; Marshall, G.R. Computer-assisted analysis of bioactivity. I. Active conformation of histamine H1 receptor antagonists. Eur. J. Med. Chem., 1985, 20, 529-534.
    • (1985) Eur. J. Med. Chem. , vol.20 , pp. 529-534
    • Naruto, S.1    Motoc, I.2    Marshall, G.R.3
  • 150
    • 0028182504 scopus 로고
    • Drug therapy: The pharmacology and use of H1- receptor antagonist drugs
    • Simons, F.E.; Simons, K.J. Drug therapy: The pharmacology and use of H1- receptor antagonist drugs. N. Engl. J. Med., 1994, 330, 1663-1670.
    • (1994) N. Engl. J. Med. , vol.330 , pp. 1663-1670
    • Simons, F.E.1    Simons, K.J.2
  • 153
    • 0026936736 scopus 로고
    • Synthesis of N- heteryl-ć-[(2- alkoxyethyl)oxy]/ć[[2-N,N- dialkylamino) ethyl]oxy]acetamides as possible H1- antihistaminics
    • Rao, A.R.; Reddy, V.M. Synthesis of N- heteryl-ć-[(2- alkoxyethyl)oxy]/ć[[2-N,N-dialkylamino) ethyl]oxy]acetamides as possible H1- antihistaminics. Pharmazie, 1992, 47, 794-796.
    • (1992) Pharmazie , vol.47 , pp. 794-796
    • Rao, A.R.1    Reddy, V.M.2
  • 154
    • 0024600195 scopus 로고
    • Synthesis of 3-[2-(2,3-dihydro-5-phenyl-4-substituted-3H-1,2,4-triazole- 3-thione-2 -yl)-acetylamino]-2-methyl-4(3H)-quinazolinones and their pharmacological activities
    • DOI 10.1002/ardp.19893220112
    • Buyuktimkin, S.; Buyuktimkin, N.; Ozdemir, O.; Rollas, S. Quinazolinones,13. Comm. Synthesis of 3-[2-(2,3-dihydro-5-phenyl-4- substituted-3H-1,2,4-triazole-3-thione-2-yl)-acetylamino]-2-methyl-4(3H)- quinazolinones and their pharmacological activities. Arch. Pharm., 1989, 322, 49-51. (Pubitemid 19033310)
    • (1989) Archiv der Pharmazie , vol.322 , Issue.1 , pp. 49-51
    • Buyuktimkin, S.1    Buyuktimkin, N.2    Ozdemir, O.3    Rollas, S.4
  • 155
    • 40749118989 scopus 로고    scopus 로고
    • New antihistaminic agents: Synthesis and evaluation of H1 antihistaminic actions 3-[(N,N-dialkylamino)- alkyl]-1,2,3,4-tetrahydro-(1H)-thioquinazolin- 4(3H)-ones and their oxo analogues
    • Raju, M.B.; Singh, S.D.; Rao, R.R.; Rajan, K.S. New antihistaminic agents: Synthesis and evaluation of H1 antihistaminic actions 3-[(N,N-dialkylamino)- alkyl]-1,2,3,4-tetrahydro-(1H)-thioquinazolin-4(3H)-ones and their oxo analogues. Indian J. Pharm. Sci., 2007, 69(6), 853-856.
    • (2007) Indian J. Pharm. Sci. , vol.69 , Issue.6 , pp. 853-856
    • Raju, M.B.1    Singh, S.D.2    Rao, R.R.3    Rajan, K.S.4
  • 156
    • 54249105961 scopus 로고    scopus 로고
    • Synthesis and pharmacological investigation of novel 4-(2-methylphenyl)- 1-substituted-4H-[1,2,4]triazolo[4,3-A]quinazolin- 5-ones as new class of H1-antihistaminic agents
    • Alagarsamy, V.; Rupeshkumar, M.; Kavitha, K.; Meena, S.; Shankar, D.; Siddiqui, A.A.; Rajesh, R. Synthesis and pharmacological investigation of novel 4-(2-methylphenyl)-1-substituted-4H-[1,2,4]triazolo[4,3-a]quinazolin- 5-ones as new class of H1-antihistaminic agents. Eur. J. Med. Chem., 2008, 43, 2331-2337.
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 2331-2337
    • Alagarsamy, V.1    Rupeshkumar, M.2    Kavitha, K.3    Meena, S.4    Shankar, D.5    Siddiqui, A.A.6    Rajesh, R.7
  • 158
    • 0034110864 scopus 로고    scopus 로고
    • Design synthesis and antihistaminic H1) activity of some condensed 3-aminopyrimidin- 4(3H)-ones
    • 351ć358
    • Shishoo, C.J.; Shirsath, V.S.; Rathod, I.S.; Yande, V.D. Design, synthesis and antihistaminic (H1) activity of some condensed 3-aminopyrimidin- 4(3H)-ones. Eur. J. Med. Chem., 2000, 35, 351ć358.
    • (2000) Eur. J. Med. Chem. , pp. 35
    • Shishoo, C.J.1    Shirsath, V.S.2    Rathod, I.S.3    Yande, V.D.4
  • 160
    • 79952759728 scopus 로고    scopus 로고
    • Synthesis of some novel 2,5- disubstituted thiazolidinones from a long chain fatty acid as possible antiinflammatory and hydrogen peroxide scavenging agents
    • doi 10.3109/14756366.2010.489897
    • Kumar, V.; Sharma, A.; Sharma P.C. Synthesis of some novel 2,5- disubstituted thiazolidinones from a long chain fatty acid as possible antiinflammatory and hydrogen peroxide scavenging agents. J. Enz. Inhib. Med. Chem., 2011, 26(2), 198-203. doi 10.3109/14756366.2010.489897.
    • (2011) J. Enz. Inhib. Med. Chem. , vol.26 , Issue.2 , pp. 198-203
    • Kumar, V.1    Sharma, A.2    Sharma, P.C.3
  • 161
    • 43049161063 scopus 로고    scopus 로고
    • 4-Thiazolidinone- A biologically active scaffold
    • Verma, A.; Saraf, S.K. 4-Thiazolidinone- A biologically active scaffold. Eur. J. Med. Chem., 2008, 43, 897-905.
    • (2008) Eur. J. Med. Chem. , vol.43 , pp. 897-905
    • Verma, A.1    Saraf, S.K.2
  • 163
    • 34848833797 scopus 로고    scopus 로고
    • Synthesis of some novel oxadiazole and oxadiazoline analogues for their antiinflammatory activity
    • DOI 10.1248/yakushi.127.1757
    • Rajak, H.; Kharya, M.D.; Mishra, P. Synthesis of some novel oxadiazole and oxadiazole analogues for their anti inflammatory activity. Yaku Zasshi (J. Pharm. Soc. Japan), 2007, 127(10), 1757-1764. (Pubitemid 47511082)
    • (2007) Yakugaku Zasshi , vol.127 , Issue.10 , pp. 1757-1764
    • Rajak, H.1    Kharya, M.D.2    Mishra, P.3
  • 164
    • 77954416661 scopus 로고    scopus 로고
    • Design synthesis and pharmacological evaluation of some novel oxadiazole and oxadiazoline analogues as anti- inflammatory agents
    • Rajak, H.; Verasamy, R.; Singour, P.; Kharya, M.D.; Mishra, P. Design, synthesis and pharmacological evaluation of some novel oxadiazole and oxadiazoline analogues as anti- inflammatory agents J. Enz. Inhib. Med. Chem., 2010, 25(4), 492-501.
    • (2010) J. Enz. Inhib. Med. Chem. , vol.25 , Issue.4 , pp. 492-501
    • Rajak, H.1    Verasamy, R.2    Singour, P.3    Kharya, M.D.4    Mishra, P.5
  • 165
    • 80052029882 scopus 로고    scopus 로고
    • Synthesis and evaluation of novel prodrugs of naproxen. Med. Chem
    • doi 10.1007/s00044-010-9364-8
    • Sharma, P.C.; Yadav, S.; Pahwa, R.; Kaushik, D.; Jain, S. Synthesis and evaluation of novel prodrugs of naproxen. Med. Chem. Res. 2011, 20(5), 648-655. doi 10.1007/s00044-010-9364-8.
    • (2011) Res , vol.20 , Issue.5 , pp. 648-655
    • Sharma, P.C.1    Yadav, S.2    Pahwa, R.3    Kaushik, D.4    Jain, S.5
  • 166
    • 76749144263 scopus 로고    scopus 로고
    • Synthesis and antiinflammatory activity of some novel biphenyl-4-carboxylic acid 5-(arylidene)-2-(aryl)-4- oxothiazolidin-3-yl amides
    • Aakashdeep.; Jain, S.; Sharma, P.C. Synthesis and antiinflammatory activity of some novel biphenyl-4-carboxylic acid 5-(arylidene)-2-(aryl)-4- oxothiazolidin-3-yl amides. Acta Pol. Pharm. Drug Res., 2010, 67(1), 63-67.
    • (2010) Acta Pol. Pharm. Drug Res. , vol.67 , Issue.1 , pp. 63-67
    • Aakashdeep Jain, S.1    Sharma, P.C.2
  • 167
    • 0032283008 scopus 로고    scopus 로고
    • Synthesis and antiinflammatory activity of some 6-bromo-2,3- disubstituted-4 (3H)-quinazolinones
    • Saravanam, J.; Mohan, S.; Manjunatha, K.S. Synthesis and antiinflammatory activity of some 6-bromo-2,3-disubstituted-4(3H)- quinazolinones. Indian J. Heterocyl. Chem., 1998, 8, 55-58. (Pubitemid 128540662)
    • (1998) Indian Journal of Heterocyclic Chemistry , vol.8 , Issue.1 , pp. 55-58
    • Saravanan, J.1    Mohan, S.2    Manjunatha, K.S.3
  • 168
    • 0032758653 scopus 로고    scopus 로고
    • 2-substituted-3-(4-bromo-2-carboxyphenyl)-5-methyl-4-thiazolidinones as potential anti inflammatory agents
    • Goel, B.; Ram, T.; Tyagi, R.; Bansal, E.; Kumar, A.; Mukerjee, D.; Sinha, J.N. 2-substituted-3-(4-bromo-2-carboxyphenyl)-5-methyl-4-thiazolidinones as potential anti inflammatory agents. Eur. J. Med. Chem., 1999, 34(3), 265-269.
    • (1999) Eur. J. Med. Chem. , vol.34 , Issue.3 , pp. 265-269
    • Goel, B.1    Ram, T.2    Tyagi, R.3    Bansal, E.4    Kumar, A.5    Mukerjee, D.6    Sinha, J.N.7
  • 169
    • 0242298226 scopus 로고    scopus 로고
    • Some new 2,3,6-trisubstituted quinazolinones as potent anti-inflammatory, analgesic and COX-II inhibitors
    • DOI 10.1016/S0968-0896(03)00501-7
    • Kumar, A.; Sharma, S.; Archana.; Bajaj, K.; Sharma, S.; Panwar, H.; Singh, T.; Srivastava, V.K. Some new 2,3,6-trisubstituted quinazolinones as potent anti inflammatory, analgesic and COX-II inhibitors. Bioorg. Med. Chem., 2003, 11, 5293-5299. (Pubitemid 37353016)
    • (2003) Bioorganic and Medicinal Chemistry , vol.11 , Issue.23 , pp. 5293-5299
    • Kumar, A.1    Sharma, S.2    Archana3    Bajaj, K.4    Sharma, S.5    Panwar, H.6    Singh, T.7    Srivastava, V.K.8
  • 170
    • 33846283385 scopus 로고    scopus 로고
    • The evolution of gene regulation by transcription factors and micro RNAs
    • Kevin, C.; Nikolaus, R. The evolution of gene regulation by transcription factors and micro RNAs. Nat. Rev. Genet., 2007, 8(2), 93-103.
    • (2007) Nat. Rev. Genet. , vol.8 , Issue.2 , pp. 93-103
    • Kevin, C.1    Nikolaus, R.2
  • 171
    • 62749101188 scopus 로고    scopus 로고
    • Design synthesis and characterization of novel 2-(2,4-disubstituted- thiazole-5-yl)-3-aryl-3H-quinazoline-4-one derivatives as inhibitors of NF-kB and AP-1 mediated transcription activation and as potential anti-inflammatory agents
    • Giri, R.S.; Thaker, H.M.; Giordano, T.; Williams, J.; Rogers, D.; Sudersanam, V.; Vasu, K.K. Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3H-quinazoline-4-one derivatives as inhibitors of NF-kB and AP-1 mediated transcription activation and as potential anti-inflammatory agents. Eur. J. Med. Chem., 2009, 44, 2184-2189.
    • (2009) Eur. J. Med. Chem , vol.44 , pp. 2184-2189
    • Giri, R.S.1    Thaker, H.M.2    Giordano, T.3    Williams, J.4    Rogers, D.5    Sudersanam, V.6    Vasu, K.K.7
  • 172
    • 57949096601 scopus 로고    scopus 로고
    • Synthesis and anti inflammatory activity of newer quinazolin-4-ones. Eur
    • Kumar, A.; Rajput, C.S. Synthesis and anti inflammatory activity of newer quinazolin-4-ones. Eur. J. Med. Chem., 2009; 44: 83-90.
    • (2009) J. Med. Chem. , vol.44 , pp. 83-90
    • Kumar, A.1    Rajput, C.S.2
  • 173
    • 33644941061 scopus 로고    scopus 로고
    • Nonsteroidal anti inflammatory agents-part 2 antiinflammatory, analgesic and antipyretic activity of some substituted 3-pyrazolin-5-ones and 1,2,4,5,6,7-3Hhexahydroindazol- 3-ones
    • Hawash, A.M.; Badawey, A.M.; Ashmawey, I.M. Nonsteroidal anti inflammatory agents-part 2 antiinflammatory, analgesic and antipyretic activity of some substituted 3-pyrazolin-5-ones and 1,2,4,5,6,7-3Hhexahydroindazol- 3-ones. Eur. J. Med. Chem., 2006, 41, 155-165.
    • (2006) Eur. J. Med. Chem. , vol.41 , pp. 155-165
    • Hawash, A.M.1    Badawey, A.M.2    Ashmawey, I.M.3
  • 174
    • 33750949952 scopus 로고    scopus 로고
    • Synthesis and pharmacological evaluation of some 3-phenyl-2-substituted- 3H-quinazolin-4-one as analgesic, anti-inflammatory agents
    • DOI 10.1016/j.bmc.2006.09.065, PII S0968089606008108
    • Alagarsamy, V.; Solomon, V.R.; Dhanabal, K. Synthesis and pharmacological evaluation of some 3-phenyl-2-substituted-3H-quinazolin- 4-one as analgesic, anti-inflammatory agents. Bioorg. Med. Chem., 2007, 15, 235-241. (Pubitemid 44738581)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.1 , pp. 235-241
    • Alagarsamy, V.1    Raja Solomon, V.2    Dhanabal, K.3
  • 175
    • 33947096571 scopus 로고    scopus 로고
    • Synthesis of 3-[4′-(p-chlorophenyl)-thiazol-2′-yl]-2- [(substituted azetidinone/thiazolidinone)-aminomethyl]-6-bromoquinazolin-4-ones as anti-inflammatory agent
    • DOI 10.1016/j.bmc.2007.01.042, PII S0968089607000673
    • Kumar, A.; Rajput, C.S.; Bhati, S.K. Synthesis of 3-[4-(p-chlorophenyl)- thiazol-2-yl]-2-[(substituted azetidinone/thiazolidinone)-aminomethyl]-6- bromoquinazolin-4-ones as anti-inflammatory agent. Bioorg. Med. Chem., 2007, 15, 3089-3096. (Pubitemid 46400456)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.8 , pp. 3089-3096
    • Kumar, A.1    Rajput, C.S.2    Bhati, S.K.3
  • 176
    • 70350511195 scopus 로고    scopus 로고
    • Novel 3-(p-substituted phenyl)-6-bromo-4(3H)-quinazolinone derivatives of promising anti-inflammatory and analgesic properties
    • Mohamed, M.S.; Kamel, M.M.; Kassem, E.M.M.; Abotaleb, N.; Nofel, S.M.; Ahmed, M.F. Novel 3-(p-substituted phenyl)-6-bromo-4(3H)-quinazolinone derivatives of promising anti-inflammatory and analgesic properties. Acta Pol. Pharm.Drug Res., 2009, 66(5), 487-500.
    • (2009) Acta Pol. Pharm.Drug Res. , vol.66 , Issue.5 , pp. 487-500
    • Mohamed, M.S.1    Kamel, M.M.2    Kassem, E.M.M.3    Abotaleb, N.4    Nofel, S.M.5    Ahmed, M.F.6
  • 177
    • 0033942231 scopus 로고    scopus 로고
    • Antilipidemic agents, Part IV: Synthesis and antilipidemic testing of some heterocyclic derivatives of hexadecyl and cyclohexyl hemisuccinate esters
    • Habib, N.S.; Ismail, K.A.; El-Tombary, A.A.; Abd El-Aziem, T. Antilipidemic agents, Part IV: Synthesis and antilipidemic testing of some heterocyclic derivatives of hexadecyl and cyclohexyl hemisuccinate esters. Pharmazie, 2000, 55, 495-499. (Pubitemid 30471430)
    • (2000) Pharmazie , vol.55 , Issue.7 , pp. 495-499
    • Habib, N.S.1    Ismail, K.A.2    El-Tombary, A.A.3    Aziem, T.A.4
  • 179
    • 0029881470 scopus 로고    scopus 로고
    • Synthesis and hypolipidemic activities of novel 2-(4- [(diethoxyphosphoryl) methyl]phenyl) quinazolines and 4(3H)- quinazolinones
    • Kurogi, Y.; Inoue, Y.; Tsutsumi, K.; Nakamura, S.; Nagao, K.; Yoshitsugu, H.; Tsuda, Y. Synthesis and hypolipidemic activities of novel 2-(4- [(diethoxyphosphoryl) methyl]phenyl) quinazolines and 4(3H)- quinazolinones. J. Med. Chem. 1996 39 1433-1437.
    • (1996) J. Med. Chem. , vol.39 , pp. 1433-1437
    • Kurogi, Y.1    Inoue, Y.2    Tsutsumi, K.3    Nakamura, S.4    Nagao, K.5    Yoshitsugu, H.6    Tsuda, Y.7
  • 180
  • 181
    • 0344034769 scopus 로고    scopus 로고
    • Lipoprotein abnormalities and their consequences for patients with type 2 diabetes
    • Krentz, AJ. Lipoprotein abnormalities and their consequences for patients with type 2 diabetes. Diabetes Obes. Metab., 2003, 5, 19-27.
    • (2003) Diabetes Obes. Metab. , vol.5 , pp. 19-27
    • Krentz, A.J.1
  • 182
    • 27744574330 scopus 로고    scopus 로고
    • The antihyperlipidemic activities of 4(3H)-quinazolinone and two halogenated derivatives in rats
    • Refaie, FM.; Esmat, AY.; Gawad, S.; Ibrahim, A.M.; Mohamed, M.A. The antihyperlipidemic activities of 4(3H)-quinazolinone and two halogenated derivatives in rats. Lipids in health and disease, 2005, 4(22), 1-11.
    • (2005) Lipids in health and disease , vol.4 , Issue.22 , pp. 1-11
    • Refaie, F.M.1    Esmat, A.Y.2    Gawad, S.3    Ibrahim, A.M.4    Mohamed, M.A.5
  • 183
    • 34047188045 scopus 로고    scopus 로고
    • Synthesis and antihypertensive activity of novel 3-benzyl-2-substituted- 3H-[1,2,4]triazolo[5,1-b]quinazolin-9-ones
    • DOI 10.1016/j.bmc.2007.03.007, PII S0968089607001939
    • Algarswamy, V.; Pathak, U.S. Synthesis and antihypertensive activity of novel 3-benzyl-2-substituted-3H-[1,2,4] triazolo [5,1-b]quinazolin-9-ones. Bioorg. Med. Chem., 2007, 15, 3457-3462. (Pubitemid 46529260)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.10 , pp. 3457-3462
    • Alagarsamy, V.1    Pathak, U.S.2
  • 184
    • 60449116913 scopus 로고    scopus 로고
    • An investigation leading to preparation of tetrahydro-quinazoline derivatives involving ureidoalkylation and ć-amidoalkylation reactions
    • Pandey, V.K.; Mukesh.; Kumar, A.; Trivedi, N. An investigation leading to preparation of tetrahydro-quinazoline derivatives involving ureidoalkylation and ć-amidoalkylation reactions. Indian J. Chem., 2008, 47B, 1910-1914.
    • (2008) Indian J. Chem. , vol.47 B , pp. 1910-1914
    • Pandey, V.K.1    Mukesh2    Kumar, A.3    Trivedi, N.4
  • 185
    • 0037624770 scopus 로고    scopus 로고
    • Synthesis and antihyperglycemic activity of suitably functionalized 3H-quinazolin-4-ones
    • DOI 10.1016/S0968-0896(03)00142-1
    • Ram Ji, V.; Farhanullah; Tripathi, B.K.; Srivastava, A.K. Synthesis and antihyperglycemic activity of suitably functionalized 3H-quinazolin-4-ones. Bioorg. Med. Chem., 2003, 11, 2439-2444. (Pubitemid 36539380)
    • (2003) Bioorganic and Medicinal Chemistry , vol.11 , Issue.11 , pp. 2439-2444
    • Ram, V.J.1    Farhanullah2    Tripathi, B.K.3    Srivastava, A.K.4
  • 186
    • 80054875300 scopus 로고    scopus 로고
    • Drug design based on the principle of conjunction: Synthesis, characterization and antihyperglycemic activity study of 3- [2- (3- aroyl- 2,4- diphenyl- 3 , 4- dihydro- 2h [1, 3] oxazino [5, 6-h] quinolin- 6- yl) ethyl] 2-phenyl- quinazolin- 4(3h)- ones
    • Bishnoi, A.; Awasthi, R.; Pandey, V.K.; Tiwari, A.K, Awasthi NK., Srivastava K, Singh S. Drug design based on the principle of conjunction: Synthesis, characterization and antihyperglycemic activity study of 3- [2- (3- aroyl- 2,4- diphenyl- 3 , 4- dihydro- 2h [1, 3] oxazino [5, 6-h] quinolin- 6- yl) ethyl] 2-phenyl- quinazolin- 4(3h)- ones. Int. J. Drug Disc., 2009, 1(2), 52-55.
    • (2009) Int. J. Drug Disc , vol.1 , Issue.2 , pp. 52-55
    • Bishnoi, A.1    Awasthi, R.2    Pandey, V.K.3    Tiwari, A.K.4    Awasthi, N.K.5    Srivastava, K.6    Singh, S.7
  • 189
    • 0005421573 scopus 로고    scopus 로고
    • 2nd ed.; New Age International Publishers
    • Kar, Ashutosh.; Medicinal Chemistry, 2nd ed.; New Age International Publishers, 2005, pp. 89.
    • (2005) Medicinal Chemistry , pp. 89
    • Kar, A.1
  • 190
    • 33847307512 scopus 로고    scopus 로고
    • An efficient construction of quinazolin-4(3H)-ones under microwave irradiation
    • Li, F.; Feng, Y.; Meng, Q.; Li, W.; Li, Z.; Wang, Q.; Tao, F. An efficient construction of quinazolin-4(3H)-ones under microwave irradiation. ARKIVOC, 2007, 1, 40-50.
    • (2007) ARKIVOC , vol.1 , pp. 40-50
    • Li, F.1    Feng, Y.2    Meng, Q.3    Li, W.4    Li, Z.5    Wang, Q.6    Tao, F.7
  • 192


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.