메뉴 건너뛰기




Volumn 46, Issue 12, 2003, Pages 2482-2493

Novel indolyl aryl sulfones active against HIV-1 carrying NNRTI resistance mutations: Synthesis and SAR studies

Author keywords

[No Author keywords available]

Indexed keywords

1 BENZENESULFONYLINDOLE DERIVATIVE; 2 METHYLPHENYLSULFONYL DERIVATIVE; 3 BENZENESULFONYLINDOLE DERIVATIVE; 3 METHYLPHENYLSULFONYL DERIVATIVE; 5 BROMO 3 [(3,5 DIMETHYLPHENYL)SULFONYL] 1H INDOLE 2 CARBOXAMIDE; 5 CHLORO 3 [(3,5 DIMETHYLPHENYL)SULFONYL] 1H INDOLE 2 CARBOXAMIDE; ANTIRETROVIRUS AGENT; INDOLYLSULFONE DERIVATIVE; L 737126; RNA DIRECTED DNA POLYMERASE INHIBITOR; UNCLASSIFIED DRUG;

EID: 12444315080     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm0211063     Document Type: Article
Times cited : (172)

References (17)
  • 1
    • 0032437454 scopus 로고    scopus 로고
    • The role of nonnucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection
    • (a) De Clercq, E. The role of nonnucleoside reverse transcriptase inhibitors (NNRTIs) in the therapy of HIV-1 infection. Antiviral Res. 1998, 38, 153-179.
    • (1998) Antiviral Res. , vol.38 , pp. 153-179
    • De Clercq, E.1
  • 2
    • 0029951587 scopus 로고    scopus 로고
    • Nonnucleoside anti-HIV-1 reverse transcriptase inhibitors (NNRTIs): A chemical survey from lead compounds to selected drugs for clinical trials
    • (b) Artico, M. Nonnucleoside anti-HIV-1 reverse transcriptase inhibitors (NNRTIs): a chemical survey from lead compounds to selected drugs for clinical trials. Farmaco 1996, 51, 305-331.
    • (1996) Farmaco , vol.51 , pp. 305-331
    • Artico, M.1
  • 6
    • 0030045677 scopus 로고    scopus 로고
    • 2-Sulfonyl-4-chloroanilino moiety: A potent pharmacophore for the anti-human immunodeficiency virus type 1 activity of pyrrolyl aryl sulfones
    • Artico, M.; Silvestri, R.; Massa, S.; Loi, A. G.; Corrias, S.; Piras, G.; La Colla, P. 2-Sulfonyl-4-chloroanilino Moiety: A Potent Pharmacophore for the Anti-Human Immunodeficiency Virus Type 1 Activity of Pyrrolyl Aryl Sulfones. J. Med. Chem. 1996, 39, 522-530.
    • (1996) J. Med. Chem. , vol.39 , pp. 522-530
    • Artico, M.1    Silvestri, R.2    Massa, S.3    Loi, A.G.4    Corrias, S.5    Piras, G.6    La Colla, P.7
  • 7
    • 0022378015 scopus 로고
    • A convenient synthesis of 3-acylindoles via Friedel-Crafts acylation of 1-(phenylsulfonyl)indole. A new route to pyridocarbazole-5, 11-quinones and ellipticine
    • Ketcha, D. M.; Gribble, G. W. A convenient synthesis of 3-acylindoles via Friedel-Crafts acylation of 1-(phenylsulfonyl)indole. A new route to pyridocarbazole-5, 11-quinones and ellipticine. J. Org. Chem. 1985, 26, 5451-5457.
    • (1985) J. Org. Chem. , vol.26 , pp. 5451-5457
    • Ketcha, D.M.1    Gribble, G.W.2
  • 8
    • 77954444904 scopus 로고
    • A new synthesis of 3-arylthioindoles
    • Atkinson, J. G.; Hamel, P.; Girard, Y. A new synthesis of 3-arylthioindoles. Synthesis 1988, 480-481.
    • (1988) Synthesis , pp. 480-481
    • Atkinson, J.G.1    Hamel, P.2    Girard, Y.3
  • 10
    • 0031899273 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of 5H-indolo[3,2-b] [1,5]-benzothiazepine derivatives, designed as conformationally constrained analogues of human immunodeficiency virus type 1 reverse transcriptase inhibitor L-737,126
    • Silvestri, R.; Artico, M.; Bruno, B.; Massa, S.; Novellino, E.; Greco, G.; Marongiu, M. E.; Pani, A.; De Montis, A.; La Colla, P. Synthesis and biological evaluation of 5H-indolo[3,2-b] [1,5]- benzothiazepine derivatives, designed as conformationally constrained analogues of human immunodeficiency virus type 1 reverse transcriptase inhibitor L-737,126. Antiviral Chem. Chemother. 1998, 9, 139-148.
    • (1998) Antiviral Chem. Chemother. , vol.9 , pp. 139-148
    • Silvestri, R.1    Artico, M.2    Bruno, B.3    Massa, S.4    Novellino, E.5    Greco, G.6    Marongiu, M.E.7    Pani, A.8    De Montis, A.9    La Colla, P.10
  • 11
    • 0036987892 scopus 로고    scopus 로고
    • Discovery of second generation quinazolinone non-nucleoside reverse transcriptase inhibitors of HIV-1
    • Corbett, J. M.; Rodgers, J. D. Discovery of second generation quinazolinone non-nucleoside reverse transcriptase inhibitors of HIV-1, Progress in Med. Chem. 2002, 40, 63-105.
    • (2002) Progress in Med. Chem. , vol.40 , pp. 63-105
    • Corbett, J.M.1    Rodgers, J.D.2
  • 12
  • 13
    • 33947086466 scopus 로고
    • Syntheses with N-protected 2-lithioindoles
    • Sundberg, R. J.; Russel, H. F. Syntheses with N-protected 2-lithioindoles. J. Org. Chem. 1983, 38, 3324-3330.
    • (1983) J. Org. Chem. , vol.38 , pp. 3324-3330
    • Sundberg, R.J.1    Russel, H.F.2
  • 14
    • 33845553875 scopus 로고
    • Generation and reaction of 3-lithio-1-(phenylsulfonyl) indole
    • Saulnier, M. G.; Gribble, G. W. Generation and reaction of 3-lithio-1-(phenylsulfonyl) indole. J. Org. Chem. 1982, 47, 757-761.
    • (1982) J. Org. Chem. , vol.47 , pp. 757-761
    • Saulnier, M.G.1    Gribble, G.W.2
  • 15
    • 0001074332 scopus 로고
    • Synthesis of carbazole alkaloids hyellazole and 6-chlorohyellazole
    • Kano, S.; Sugino, E.; Shibuya, S.; Hibino, S. Synthesis of carbazole alkaloids hyellazole and 6-chlorohyellazole. J. Org. Chem. 1981, 46, 3856-3859.
    • (1981) J. Org. Chem. , vol.46 , pp. 3856-3859
    • Kano, S.1    Sugino, E.2    Shibuya, S.3    Hibino, S.4
  • 17
    • 0026540533 scopus 로고
    • HIV-1 reverse transcriptase inhibition by a dipyridodiazepinone derivative BI-RG-587
    • Tramontano, E.; Cheng, Y.-C. HIV-1 reverse transcriptase inhibition by a dipyridodiazepinone derivative BI-RG-587. Biochem. Pharmacol. 1992, 43, 1371-1376.
    • (1992) Biochem. Pharmacol. , vol.43 , pp. 1371-1376
    • Tramontano, E.1    Cheng, Y.-C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.