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Volumn 19, Issue 13, 2012, Pages 2026-2037

Recent advances in the research of 2,3-diaryl-1,3-thiazolidin-4-one derivatives as potent HIV-1 non-nucleoside reverse transcriptase inhibitors

Author keywords

1,3 Thiazolidin 4 ones; AIDS; Antiviral; Drug design; HIV; HIV 1 NNRTIs

Indexed keywords

2,3 DIARYL 1,3 THIAZOLIDIN 4 ONE DERIVATIVE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; NONNUCLEOSIDE REVERSE TRANSCRIPTASE INHIBITOR; THIAZOLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84860527224     PISSN: 09298673     EISSN: 1875533X     Source Type: Journal    
DOI: 10.2174/092986712800167383     Document Type: Article
Times cited : (27)

References (56)
  • 1
    • 0033534386 scopus 로고    scopus 로고
    • Structural biology of HIV
    • DOI 10.1006/jmbi.1998.2354
    • Turner, B.G.; Summers, M.F., Structural biology of HIV. J. Mol. Biol., 1999, 285, (1), 1-32. (Pubitemid 29034021)
    • (1999) Journal of Molecular Biology , vol.285 , Issue.1 , pp. 1-32
    • Turner, B.G.1    Summers, M.F.2
  • 2
    • 0034059835 scopus 로고    scopus 로고
    • The HIV-1 reverse transcription (RT) process as target for RT inhibitors
    • DOI 10.1002/(SICI)1098-1128(200003)20: 2<129::AID-MED2>3.0.CO;2-A
    • Jonckheere, H.; Anné, J.; De Clercq, E., The HIV-1 reverse transcription (RT) process as target for RT Inhibitors. Med. Res. Rev., 2000, 20, (2), 129-154. (Pubitemid 30134322)
    • (2000) Medicinal Research Reviews , vol.20 , Issue.2 , pp. 129-154
    • Jonckheere, H.1    Anne, J.2    De Clercq, E.3
  • 3
    • 0034100184 scopus 로고    scopus 로고
    • Nonnucleoside reverse transcriptase inhibitors
    • Hajos, G.; Riedl, Z.; Molnar, J.; Szabo, D., Nonnucleoside reverse transcriptase inhibitors. Drugs of the Future, 2000, 25, (2), 47-62. (Pubitemid 30120988)
    • (2000) Drugs of the Future , vol.25 , Issue.1 , pp. 47-62
    • Hajos, G.1    Riedl, Z.2    Molnar, J.3    Szabo, D.4
  • 5
    • 0033014605 scopus 로고    scopus 로고
    • Guide to major clinical trials of antiretroviral therapy in human immunodeficiency virus-infected patients: Protease inhibitors, non-nucleoside reverse transcriptase inhibitors, and nucleotide reverse transcriptase inhibitors
    • Tavel, J.A.; Miller, K.D.; Masur, H., Guide to major clinical trials of antiretroviral therapy in human immunodeficiency virus-infected patients: protease inhibitors, non-nucleoside reverse transcriptase inhibitors, and nucleotide reverse transcriptase inhibitors. Clin. Infect. Dis., 1999, 28, (3), 643-676. (Pubitemid 29242549)
    • (1999) Clinical Infectious Diseases , vol.28 , Issue.3 , pp. 643-676
    • Tavel, J.A.1    Miller, K.D.2    Masur, H.3
  • 6
    • 15444380338 scopus 로고    scopus 로고
    • From 4,5,6,7-tetrahydro-5-methylimidazo[4,5,1-jk](1,4)benzodiazepin-2(1H) - one (TIBO) to etravirine (TMC125): Fifteen years of research on non-nucleoside inhibitors of HIV-1 reverse transcriptase
    • DOI 10.1021/jm040127p
    • De Corte, B.L., From 4,5,6,7-tetrahydro-5-methylimidazo[4,5,1-jk](1,4) benzodiazepin-2(1H)-one (TIBO) to etravirine (TMC125): fifteen years of research on non-nucleoside inhibitors of HIV-1 reverse transcriptase. J. Med. Chem., 2005, 48, (6), 1689-1696. (Pubitemid 40396298)
    • (2005) Journal of Medicinal Chemistry , vol.48 , Issue.6 , pp. 1689-1696
    • De Corte, B.L.1
  • 8
    • 84860540088 scopus 로고    scopus 로고
    • U.S. Food and Drug Administration, (Accessed May 20, 2011)
    • U.S. Food and Drug Administration. FDA Approves New HIV Treatment. http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm256087.htm (Accessed May 20, 2011).
    • FDA Approves New HIV Treatment
  • 9
    • 0026324187 scopus 로고
    • Anti-HIV agents. I: Synthesis and in vitro anti-HIV evaluation of novel 1H,3Hthiazolo[ 3,4-a]benzimidazoles
    • Chimirri, A.; Grasso, S.; Monforte, A.M.; Monforte, P.; Zappalà, M., Anti-HIV agents. I: synthesis and in vitro anti-HIV evaluation of novel 1H,3Hthiazolo[ 3,4-a]benzimidazoles. Farmaco, 1991, 46, (6), 817-823.
    • (1991) Farmaco , vol.46 , Issue.6 , pp. 817-823
    • Chimirri, A.1    Grasso, S.2    Monforte, A.M.3    Monforte, P.4    Zappalà, M.5
  • 10
    • 0025812546 scopus 로고
    • Anti-HIV agents II. synthesis and in vitro anti-HIV activity of novel 1H,3Hthiazolo[ 3,4-a]benzimidazoles
    • Chimirri, A.; Grasso, S.; Monforte, A.M.; Monforte, P.; Zappalà, M., Anti-HIV agents II. synthesis and in vitro anti-HIV activity of novel 1H,3Hthiazolo[ 3,4-a]benzimidazoles. Farmaco, 1991, 46, (7-8), 925-933.
    • (1991) Farmaco , vol.46 , Issue.7-8 , pp. 925-933
    • Chimirri, A.1    Grasso, S.2    Monforte, A.M.3    Monforte, P.4    Zappalà, M.5
  • 11
    • 0030814399 scopus 로고    scopus 로고
    • Structural features and anti-human immunodeficiency virus (HIV) activity of the isomers of 1-(2',6'-difluorophenyl)-1H,3H-thiazolo[3,4-a] benzimidazole, a potent non-nucleoside HIV-1 reverse transcriptase inhibitor
    • Chimirri, A.; Grasso, S.; Molica, C.; Monforte, A.M.; Monforte, P.; Zappalà, M.; Bruno, G.; Nicolò, F.; Witvrouw, M.; Jonckeere, H.; Balzarini, J.; De Clercq, E., Structural features and anti-human immunodeficiency virus (HIV) activity of the isomers of 1-(2',6'-difluorophenyl) -1H,3H-thiazolo[3,4-a]benzimidiazole, a potent non-nucleoside HIV-1 reverse transcriptase inhibitor. Antivir.Chem.Chemother, 1997, 8, 363-370. (Pubitemid 27292638)
    • (1997) Antiviral Chemistry and Chemotherapy , vol.8 , Issue.4 , pp. 363-370
    • Chimirri, A.1    Grasso, S.2    Molica, C.3    Monforte, A.-M.4    Monforte, P.5    Zappala, M.6    Bruno, G.7    Nicolo, F.8    Witvrouw, M.9    Jonckeere, H.10    Balzarini, J.11    De Clercq, E.12
  • 12
    • 0031181346 scopus 로고    scopus 로고
    • QXP: Powerful, rapid computer algorithms for structure-based drug design
    • McMartin, C.; Bohacek, R.S., QXP: Powerful, rapid computer algorithms for structure-based drug design. J. Comput. Aided Mol. Des., 1997, 11, (4), 333-344. (Pubitemid 127506740)
    • (1997) Journal of Computer-Aided Molecular Design , vol.11 , Issue.4 , pp. 333-344
    • McMartin, C.1    Bohacek, R.S.2
  • 13
    • 0033491040 scopus 로고    scopus 로고
    • Comparative molecular field analysis (CoMFA) and docking studies of non- nucleoside HIV-1 RT inhibitors (NNIs)
    • DOI 10.1016/S0968-0896(99)00181-9, PII S0968089699001819
    • Barreca, M.L.; Carotti, A.; Carrieri, A.; Chimirri, A.; Monforte, A.M.; Pellegrini Calace, M.; Rao, A., Comparative molecular field analysis (CoMFA) and docking studies of non-nucleoside HIV-1 RT inhibitors (NNIs). Bioorg. Med. Chem., 1999, 7, (11), 2283-2292. (Pubitemid 30122730)
    • (1999) Bioorganic and Medicinal Chemistry , vol.7 , Issue.11 , pp. 2283-2292
    • Barreca, M.L.1    Carotti, A.2    Carrieri, A.3    Chimirri, A.4    Monforte, A.M.5    Pellegrini Calace, M.6    Rao, A.7
  • 15
    • 0031433445 scopus 로고    scopus 로고
    • Anti-HIV agents. v. synthesis, structure and in vitro anti-HIV activity of novel 1H,3H-naphtho[2',3':4,5]imidazo[1,2-c]thiazoles
    • Chimirri, A.; Grasso, S.; Monforte, A.M.; Monforte, P.; Rao, A.; Zappalà, M.; Bruno, G.; Nicolo, F.; Scopelliti, R., Anti-HIV agents. V. Synthesis, structure and in vitro anti-HIV activity of novel 1H,3H-naphtho[2 ′,3 ′: 4,5]imidazo[1,2-c]thiazoles. Farmaco, 1997, 52, (11), 673-677. (Pubitemid 28167892)
    • (1997) Farmaco , vol.52 , Issue.11 , pp. 673-677
    • Chimirri, A.1    Grasso, S.2    Monforte, A.-M.3    Monforte, P.4
  • 16
    • 0031463691 scopus 로고    scopus 로고
    • Synthesis and biological activity of novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 2-Aryl-substituted benzimidazoles
    • DOI 10.1021/jm970096g
    • Roth, T.; Morningstar, M.L.; Boyer, P.L.; Hughes, S.H.; Buckheit, R.W.; Michejda, C.J., Synthesis and biological activity of novel nonnucleoside inhibitors of HIV-1 reverse transcriptase. 2-Aryl-substituted benzimidazoles. J. Med. Chem., 1997, 40, (26), 4199-4207. (Pubitemid 28042301)
    • (1997) Journal of Medicinal Chemistry , vol.40 , Issue.26 , pp. 4199-4207
    • Roth, T.1    Morningstar, M.L.2    Boyer, P.L.3    Hughes, S.H.4    Buckheit Jr., R.W.5    Michejda, C.J.6
  • 19
    • 0034163201 scopus 로고    scopus 로고
    • Synthesis and structural features of new cyclofunctionalized benzimidazoles
    • Chimirri, A.; Monforte, A.M.; Monforte, P.; Nicolo, F.; Rao, A.; Zappalà, M., Synthesis and structural features of new cyclofunctionalized benzimidazoles. Heterocycles, 2000, 53, (3), 613-620.
    • (2000) Heterocycles , vol.53 , Issue.3 , pp. 613-620
    • Chimirri, A.1    Monforte, A.M.2    Monforte, P.3    Nicolo, F.4    Rao, A.5    Zappalà, M.6
  • 20
    • 0034797941 scopus 로고    scopus 로고
    • Synthesis, biological activity, pharmacokinetic properties and molecular modelling studies of novel 1H,3H-oxazolo[3,4-a]benzimidazoles: Non-nucleoside HIV-1 reverse transcriptase inhibitors
    • Chimirri, A.; Monforte, P.; Rao, A.; Zappalà, M.; Monforte, A.M.; De Sarro, G.; Pannecouque, C.; Witvrouw, M.; Balzarini, J.; De Clercq, E., Synthesis, biological activity, pharmacokinetic properties and molecular modelling studies of novel 1H,3H-oxazolo[3,4-a]benzimidazoles: non-nucleoside HIV-1 reverse transcriptase inhibitors. Antivir Chem Chemother, 2001, 12, (3), 169-174. (Pubitemid 32963916)
    • (2001) Antiviral Chemistry and Chemotherapy , vol.12 , Issue.3 , pp. 169-174
    • Chimirri, A.1    Monforte, P.2    Rao, A.3    Zappala, M.4    Monforte, A.M.5    De Sarro, G.6    Pannecouque, C.7    Witvrouw, M.8    Balzarini, J.9    De Clercq, E.10
  • 21
    • 1842866611 scopus 로고    scopus 로고
    • Synthesis and anti-HIV activity of 1-(2,6-difluorophenyl)-1H,3H- thiazolo[3,4-a]benzimidazole structurally-related 1,2-substituted benzimidazoles
    • DOI 10.1016/S0014-827X(02)01300-9, PII S0014827X02013009
    • Rao, A.; Chimirri, A.; De Clercq, E.; Monforte, A.M.; Monforte, P.; Pannecouque, C.; Zappalà, M., Synthesis and anti-HIV activity of 1-(2,6-difluorophenyl)-1H,3H-thiazolo[3,4-a]benzimidazole structurally-related 1,2-substituted benzimidazoles. Il Farmaco, 2002, 57, (10), 819-823. (Pubitemid 35440977)
    • (2002) Farmaco , vol.57 , Issue.10 , pp. 819-823
    • Rao, A.1    Chimirri, A.2    De Clercq, E.3    Monforte, A.M.4    Monforte, P.5    Pannecouque, C.6    Zappala, M.7
  • 25
    • 34447569299 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 2,3-diaryl substituted-1,3 thiazolidin-4-ones as anti-HIV agents
    • DOI 10.2174/157340607781024393
    • Rawal, R.K.; Tripathi, R.K.; Katti, S.B.; Pannecouque, C.; De Clercq, E., Synthesis and biological evaluation of 2,3-diaryl substituted-1,3-thiazolidin- 4-ones as anti-HIV agents. Medicinal Chemistry, 2007, 3, (4), 355-363. (Pubitemid 47082999)
    • (2007) Medicinal Chemistry , vol.3 , Issue.4 , pp. 355-363
    • Rawal, R.K.1    Tripathi, R.K.2    Katti, S.B.3    Pannecouque, C.4    De Clercq, E.5
  • 26
    • 0037320465 scopus 로고    scopus 로고
    • Synthesis and anti-HIV activity of 2,3-diaryl-1,3-thiazolidin-4-ones
    • DOI 10.1016/S0014-827X(02)00024-1, PII S0014827X02000241
    • Rao, A.; Carbone, A.; Chimirri, A.; De Clercq, E.; Monforte, A.M.; Monforte, P.; Pannecouque, C.; Zappalà, M., Synthesis and anti-HIV activity of 2,3-diaryl-1,3-thiazolidin-4-ones. Il Farmaco, 2003, 58, (2), 115-120. (Pubitemid 36197647)
    • (2003) Farmaco , vol.58 , Issue.2 , pp. 115-120
    • Rao, A.1    Carbone, A.2    Chimirri, A.3    De Clercq, E.4    Monforte, A.M.5    Monforte, P.6    Pannecouque, C.7    Zappala, M.8
  • 28
    • 4043172745 scopus 로고    scopus 로고
    • 2-(2,6-Dihalophenyl)-3-(pyrimidin-2-yl)-1,3-thiazolidin-4-ones as non-nucleoside HIV-1 reverse transcriptase inhibitors
    • DOI 10.1016/j.antiviral.2004.03.004, PII S0166354204000841
    • Rao, A.; Balzarini, J.; Carbone, A.; Chimirri, A.; De Clercq, E.; Monforte, A.M.; Monforte, P.; Pannecouque, C.; Zappalà, M., 2-(2,6-Dihalophenyl)-3-(pyrimidin-2-yl)-1,3-thiazolidin-4-ones as non-nucleoside HIV-1 reverse transcriptase inhibitors. Antiviral Res., 2004, 63, (2), 79-84. (Pubitemid 39061772)
    • (2004) Antiviral Research , vol.63 , Issue.2 , pp. 79-84
    • Rao, A.1    Balzarini, J.2    Carbone, A.3    Chimirri, A.4    De Clercq, E.5    Monforte, A.M.6    Monforte, P.7    Pannecouque, C.8    Zappala, M.9
  • 29
    • 33947580188 scopus 로고    scopus 로고
    • Synthesis and evaluation of 2-(2,6-dihalophenyl)-3-pyrimidinyl-1,3- thiazolidin-4-one analogues as anti-HIV-1 agents
    • DOI 10.1016/j.bmc.2007.02.044, PII S0968089607001654
    • Rawal, R.K.; Tripathi, R.; Katti, S.B.; Pannecouque, C.; De Clercq, E., Synthesis and evaluation of 2-(2,6-dihalophenyl)-3-pyrimidinyl-1,3-thiazolidin- 4-one analogs as anti-HIV-1 agents. Bioorg. Med. Chem., 2007, 15, (9), 3134-3142. (Pubitemid 46484339)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.9 , pp. 3134-3142
    • Rawal, R.K.1    Tripathi, R.2    Katti, S.B.3    Pannecouque, C.4    De Clercq, E.5
  • 30
    • 8544239371 scopus 로고    scopus 로고
    • CP-MLR/PLS directed structure-activity modeling of the HIV-1 RT inhibitory activity of 2,3-diaryl-1,3-thiazolidin-4-ones
    • DOI 10.1002/qsar.200330854
    • Prabhakar, Y.S.; Solomon, V.R.; Rawal, R.K.; Gupta, M.K.; Katti, S.B., CPMLR/ PLS directed structure-activity modeling of the HIV-1 RT inhibitory activity of 2,3-diaryl-1,3-thiazolidin-4-ones. Qsar & Combinatorial Science, 2004, 23, (4), 234-244. (Pubitemid 39490415)
    • (2004) QSAR and Combinatorial Science , vol.23 , Issue.4 , pp. 234-244
    • Prabhakar, Y.S.1    Solomon, V.R.2    Rawal, R.K.3    Gupta, M.K.4    Katti, S.B.5
  • 31
    • 22444444421 scopus 로고    scopus 로고
    • Topological descriptors in modeling the HIV inhibitory activity of 2-aryl-3-pyridyl-thiazolidin-4-ones
    • DOI 10.2174/1386207054546531
    • Prabhakar, Y.S.; Rawal, R.K.; Gupta, M.K.; Solomon, V.R.; Katti, S.B., Topological descriptors in modeling the HIV inhibitory activity of 2-aryl-3-pyridyl-thiazolidin-4-ones. Combinatorial Chemistry & High Throughput Screening, 2005, 8, (5), 431-437. (Pubitemid 41008790)
    • (2005) Combinatorial Chemistry and High Throughput Screening , vol.8 , Issue.5 , pp. 431-437
    • Prabhakar, Y.S.1    Rawal, R.K.2    Gupta, M.K.3    Solomon, V.R.4    Katti, S.B.5
  • 32
    • 23044466157 scopus 로고    scopus 로고
    • Classical QSAR modeling of anti-HIV 2,3-diaryl-1,3-thiazolidin-4-ones
    • DOI 10.1002/qsar.200430901
    • Roy, K.; Leonard, J.T., Classical QSAR modeling of anti-HIV 2,3-diaryl-1,3-thiazolidin-4-ones. Qsar & Combinatorial Science, 2005, 24, (5), 579-592. (Pubitemid 41074326)
    • (2005) QSAR and Combinatorial Science , vol.24 , Issue.5 , pp. 579-592
    • Roy, K.1    Leonard, J.T.2
  • 33
    • 65649125313 scopus 로고    scopus 로고
    • Design, microwave-assisted synthesis and HIV-RT inhibitory activity of 2-(2,6-dihalophenyl)-3-(4,6-dimethyl-5-(un)substituted-pyrimidin-2-yl) thiazolidin-4-ones
    • Chen, H.; Bai, J.; Jiao, L.L.; Guo, Z.H.; Yin, Q.M.; Li, X.L., Design, microwave-assisted synthesis and HIV-RT inhibitory activity of 2-(2,6-dihalophenyl)-3-(4,6-dimethyl-5-(un)substituted-pyrimidin-2-yl) thiazolidin-4-ones. Bioorg. Med. Chem., 2009, 17, (11), 3980-3986.
    • (2009) Bioorg. Med. Chem. , vol.17 , Issue.11 , pp. 3980-3986
    • Chen, H.1    Bai, J.2    Jiao, L.L.3    Guo, Z.H.4    Yin, Q.M.5    Li, X.L.6
  • 34
    • 33847781693 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of 2-aryl-3-heteroaryl-1,3-thiazolidin- 4-ones as anti-HIV agents
    • DOI 10.1016/j.bmc.2006.12.003, PII S0968089606009898
    • Rawal, R.K.; Tripathi, R.; Katti, S.B.; Pannecouque, C.; De Clercq, E., Design, synthesis, and evaluation of 2-aryl-3-heteroaryl-1,13-thiazolidin-4-ones as anti-HIV agents. Bioorg. Med. Chem., 2007, 15, (4), 1725-1731. (Pubitemid 46394053)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.4 , pp. 1725-1731
    • Rawal, R.K.1    Tripathi, R.2    Katti, S.B.3    Pannecouque, C.4    De Clercq, E.5
  • 35
    • 27644537621 scopus 로고    scopus 로고
    • 2-(Aryl)-3-furan-2-ylmethyl-thiazolidin-4-ones as selective HIV-RT Inhibitors
    • DOI 10.1016/j.bmc.2005.07.063, PII S0968089605007285
    • Rawal, R.K.; Prabhakar, Y.S.; Katti, S.B.; De Clercq, E., 2-(Aryl)-3-furan-2-ylmethyl-thiazolidin-4-ones as selective HIV-RT inhibitors. Bioorg. Med. Chem., 2005, 13, (24), 6771-6776. (Pubitemid 41571222)
    • (2005) Bioorganic and Medicinal Chemistry , vol.13 , Issue.24 , pp. 6771-6776
    • Rawal, R.K.1    Prabhakar, Y.S.2    Katti, S.B.3    De Clercq, E.4
  • 39
    • 34250676593 scopus 로고    scopus 로고
    • Molecular surface features in modeling the HIV-1 RT inhibitory activity of 2-(2,6-disubstituted phenyl)-3-(substituted pyrimidin-2-yl)-thiazolidin-4- ones
    • DOI 10.1002/qsar.200630040
    • Rawal, R.K.; Prabhakar, Y.S.; Katti, S.B., Molecular surface features in modeling the HIV-1 RT inhibitory activity of 2-(2,6-disubstituted phenyl)-3-(substituted pyrimidin-2-yl)-thiazolidin-4-ones. Qsar & Combinatorial Science, 2007, 26, (3), 398-406. (Pubitemid 46932866)
    • (2007) QSAR and Combinatorial Science , vol.26 , Issue.3 , pp. 398-406
    • Rawal, R.K.1    Prabhakar, Y.S.2    Katti, S.B.3
  • 40
  • 41
    • 0036754669 scopus 로고    scopus 로고
    • Synthesis and anti-HIV activity of 2,3-diaryl-1,3-thiazolidin-4-(thi)one derivatives
    • DOI 10.1016/S0014-827X(02)01268-5, PII S0014827X02012685
    • Rao, A.; Carbone, A.; Chimirri, A.; De Clercq, E.; Monforte, A.M.; Monforte, P.; Pannecouque, C.; Zappalà, M., Synthesis and anti-HIV activity of 2,3-diaryl-1,3-thiazolidin-4-(thi)one derivatives. Il Farmaco, 2002, 57, (9), 747-751. (Pubitemid 35287009)
    • (2002) Farmaco , vol.57 , Issue.9 , pp. 747-751
    • Rao, A.1    Carbone, A.2    Chimirri, A.3    De Clercq, E.4    Monforte, A.M.5    Monforte, P.6    Pannecouque, C.7    Zappala, M.8
  • 42
    • 77955615630 scopus 로고    scopus 로고
    • Use of the adamantane structure in medicinal chemistry
    • Lamoureux, G.; Artavia, G., Use of the adamantane structure in medicinal chemistry. Curr. Med. Chem., 2010, 17, (26), 2967-2978.
    • (2010) Curr. Med. Chem. , vol.17 , Issue.26 , pp. 2967-2978
    • Lamoureux, G.1    Artavia, G.2
  • 43
    • 34250186053 scopus 로고    scopus 로고
    • Synthesis and anti-HIV studies of 2-adamantyl-substituted thiazolidin-4-ones
    • DOI 10.1016/j.ejmech.2007.01.003, PII S0223523407000360
    • Balzarini, J.; Orzeszko, B.; Maurin, J.K.; Orzeszko, A., Synthesis and anti-HIV studies of 2-adamantyl-substituted thiazolidin-4-ones. European Journal of Medicinal Chemistry, 2007, 42, (7), 993-1003. (Pubitemid 46907342)
    • (2007) European Journal of Medicinal Chemistry , vol.42 , Issue.7 , pp. 993-1003
    • Balzarini, J.1    Orzeszko, B.2    Maurin, J.K.3    Orzeszko, A.4
  • 45
    • 77949687060 scopus 로고    scopus 로고
    • Novel thiazolidinone derivatives with an uncommon mechanism of inhibition towards HIV-1 reverse transcriptase
    • Pitta, E.; Crespan, E.; Geronikaki, A.; Maga, G.; Samuele, A., Novel thiazolidinone derivatives with an uncommon mechanism of inhibition towards HIV-1 reverse transcriptase. Letters in Drug Design & Discovery, 2010, 7, (4), 228-234.
    • (2010) Letters in Drug Design & Discovery , vol.7 , Issue.4 , pp. 228-234
    • Pitta, E.1    Crespan, E.2    Geronikaki, A.3    Maga, G.4    Samuele, A.5
  • 46
    • 7744243992 scopus 로고    scopus 로고
    • Bioisosterism: A rational approach in drug design
    • Patani, G.A.; LaVoie, E.J., Bioisosterism: a rational approach in drug design. Chem. Rev., 1996, 96, (8), 3147-3176. (Pubitemid 126641132)
    • (1996) Chemical Reviews , vol.96 , Issue.8 , pp. 3147-3176
    • Patani, G.A.1    LaVoie, E.J.2
  • 47
    • 33750701141 scopus 로고    scopus 로고
    • On scaffolds and hopping in medicinal chemistry
    • DOI 10.2174/138955706778742768
    • Brown, N.; Jacoby, E., On scaffolds and hopping in medicinal chemistry. Mini-Reviews in Medicinal Chemistry, 2006, 6, (11), 1217-1229. (Pubitemid 44697101)
    • (2006) Mini-Reviews in Medicinal Chemistry , vol.6 , Issue.11 , pp. 1217-1229
    • Brown, N.1    Jacoby, E.2
  • 50
    • 9744258219 scopus 로고    scopus 로고
    • Crystallography and the design of anti-AIDS drugs: Conformational flexibility and positional adaptability are important in the design of non-nucleoside HIV-1 reverse transcriptase inhibitors
    • DOI 10.1016/j.pbiomolbio.2004.07.001, PII S0079610704000744, Structure-Guided Design of AIDS Antivirals
    • Das, K.; Lewi, P.J.; Hughes, S.H.; Arnold, E., Crystallography and the design of anti-AIDS drugs: conformational flexibility and positional adaptability are important in the design of non-nucleoside HIV-1 reverse transcriptase inhibitors. Prog. Biophys. Mol. Biol., 2005, 88, (2), 209-231. (Pubitemid 39579659)
    • (2005) Progress in Biophysics and Molecular Biology , vol.88 , Issue.2 , pp. 209-231
    • Das, K.1    Lewi, P.J.2    Hughes, S.H.3    Arnold, E.4
  • 52
    • 33747140370 scopus 로고    scopus 로고
    • Aspects of successful drug discovery and development
    • DOI 10.1016/j.antiviral.2006.05.007, PII S0166354206001355
    • Pauwels, R., Aspects of successful drug discovery and development. Antiviral Res., 2006, 71, (2-3), 77-89. (Pubitemid 44223771)
    • (2006) Antiviral Research , vol.71 , Issue.SPEC. ISS. , pp. 77-89
    • Pauwels, R.1
  • 53
    • 70450184400 scopus 로고    scopus 로고
    • Design strategies of novel NNRTIs to overcome drug resistance
    • Zhan, P.; Liu, X.; Li, Z.; Pannecouque, C.; De Clercq, E., Design strategies of novel NNRTIs to overcome drug resistance. Curr. Med. Chem., 2009, 16, (29), 3903-3917.
    • (2009) Curr. Med. Chem. , vol.16 , Issue.29 , pp. 3903-3917
    • Zhan, P.1    Liu, X.2    Li, Z.3    Pannecouque, C.4    De Clercq, E.5
  • 54
    • 84876852661 scopus 로고    scopus 로고
    • HIV-1 NNRTIs: Structural diversity, pharmacophore similarity, and implications for drug design
    • doi: 10.1002/med.20241
    • Zhan, P.; Chen, X.; Li, D.; Fang, Z.; De Clercq, E.; Liu, X., HIV-1 NNRTIs: Structural diversity, pharmacophore similarity, and implications for drug design. Med. Res. Rev., 2011 doi: 10.1002/med.20241.
    • (2011) Med. Res. Rev.
    • Zhan, P.1    Chen, X.2    Li, D.3    Fang, Z.4    De Clercq, E.5    Liu, X.6
  • 55
    • 57049116193 scopus 로고    scopus 로고
    • Pharmacokinetic and safety evaluation of BILR 355, a secondgeneration nonnucleoside reverse transcriptase inhibitor, in healthy volunteers
    • Huang, F.; Koenen-Bergmann, M.; Macgregor, T.R.; Ring, A.; Hattox, S.; Robinson, P., Pharmacokinetic and safety evaluation of BILR 355, a secondgeneration nonnucleoside reverse transcriptase inhibitor, in healthy volunteers. Antimicrob. Agents Chemother., 2008, 52, (12), 4300-4307.
    • (2008) Antimicrob. Agents Chemother. , vol.52 , Issue.12 , pp. 4300-4307
    • Huang, F.1    Koenen-Bergmann, M.2    MacGregor, T.R.3    Ring, A.4    Hattox, S.5    Robinson, P.6


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