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Volumn 45, Issue 24, 2002, Pages 5410-5413

Design, synthesis, structure - Activity relationships, and molecular modeling studies of 2,3-diaryl-1,3-thiazolidin-4-ones as potent anti-HIV agents

Author keywords

[No Author keywords available]

Indexed keywords

ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; DELAVIRDINE; EFAVIRENZ; LIGAND; NEVIRAPINE; NUCLEOSIDE; THIAZOLIDINE DERIVATIVE;

EID: 0037153210     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm020977+     Document Type: Article
Times cited : (211)

References (11)
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    • The HIV-1 reverse transciption (RT) process as target for RT inhibitors
    • Jonckheere, H.; Anné, J.; De Clercq, E. The HIV-1 reverse transciption (RT) process as target for RT inhibitors. Med. Res. Rev. 2000, 20, 129-154.
    • (2000) Med. Res. Rev. , vol.20 , pp. 129-154
    • Jonckheere, H.1    Anné, J.2    De Clercq, E.3
  • 2
    • 0033927489 scopus 로고    scopus 로고
    • Novel compounds in preclinical/early clinical development for the treatment of HIV infections
    • De Clercq, E. Novel compounds in preclinical/early clinical development for the treatment of HIV infections. Rev. Med. Virol. 2000, 10, 255-277.
    • (2000) Rev. Med. Virol. , vol.10 , pp. 255-277
    • De Clercq, E.1
  • 3
    • 0034100184 scopus 로고    scopus 로고
    • Nonnucleoside reverse transcriptase inhibitors
    • Hajos, G.; Riedi, S.; Molnar, J.; Szabo, D. Nonnucleoside reverse transcriptase inhibitors. Drugs Fut. 2000, 25, 47-62.
    • (2000) Drugs Fut. , vol.25 , pp. 47-62
    • Hajos, G.1    Riedi, S.2    Molnar, J.3    Szabo, D.4
  • 4
  • 5
    • 0030814399 scopus 로고    scopus 로고
    • Structural features and antihuman immunodeficiency virus (HIV) activity of the isomers of 1-(2′,6′-difluorophenyl)-1H, 3H-thiazolo[3,4-a]benzimidazole, a potent nonnucleoside HIV-1 reverse transcriptase inhibitor
    • (a) Chimirri, A.; Grasso, S.; Molica, C.; Monforte, A. M.; Monforte, P.; Zappalà, M.; Bruno, G.; Nicolb, F.; Witvrouw, M.; Jonckeere, H.; Balzarini, J., De Clercq, E. Structural features and antihuman immunodeficiency virus (HIV) activity of the isomers of 1-(2′,6′-difluorophenyl)-1H, 3H-thiazolo[3,4-a]benzimidazole, a potent nonnucleoside HIV-1 reverse transcriptase inhibitor. Antiv. Chem. Chemother. 1997, 8, 363-370.
    • (1997) Antiv. Chem. Chemother. , vol.8 , pp. 363-370
    • Chimirri, A.1    Grasso, S.2    Molica, C.3    Monforte, A.M.4    Monforte, P.5    Zappalà, M.6    Bruno, G.7    Nicolb, F.8    Witvrouw, M.9    Jonckeere, H.10    Balzarini, J.11    De Clercq, E.12
  • 10
    • 0021871375 scopus 로고
    • A computational procedure for determining energetically favorable binding sites on biologically important macromolecules
    • Goodford P. J. A computational procedure for determining energetically favorable binding sites on biologically important macromolecules. J. Med. Chem. 1985, 28, 849-857.
    • (1985) J. Med. Chem. , vol.28 , pp. 849-857
    • Goodford, P.J.1
  • 11
    • 11644261806 scopus 로고    scopus 로고
    • Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function
    • Morris, G. M.; Goodsell, D. S.; Halliday, R. S.; Huey, R.; Hart, W. E.; Belew R. K.; Olson, A. J. Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function. J. Comput. Chem. 1998, 19, 1639-1662.
    • (1998) J. Comput. Chem. , vol.19 , pp. 1639-1662
    • Morris, G.M.1    Goodsell, D.S.2    Halliday, R.S.3    Huey, R.4    Hart, W.E.5    Belew, R.K.6    Olson, A.J.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.