메뉴 건너뛰기




Volumn 59, Issue 1, 2004, Pages 33-39

Synthesis of new 2,3-diaryl-1,3-thiazolidin-4-ones as anti-HIV agents

Author keywords

2,3 diaryl 1,3 thiazolidin 4 ones; Anti HIV activity; NNRTIs

Indexed keywords

2 (2 CHLORO 6 FLUORO 3 METHYLPHENYL) 3 (3 METHYLPHENYL) 1,3 THIAZOLIDIN 4 ONE; 2 (2 CHLORO 6 FLUORO 3 METHYLPHENYL) 3 (4 METHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2 CHLORO 6 FLUORO 3 METHYLPHENYL) 3 (4,6 DIMETHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2 CHLORO 6 FLUORO 3 METHYLPHENYL) 3 (6 METHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2 FLUORO 6 METHOXYPHENYL) 3 (4 METHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2 FLUORO 6 METHOXYPHENYL) 3 (6 METHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2,6 DIMETHOXYPHENYL) 3 (3 METHYLPHENYL) 1,3 THIAZOLIDIN 4 ONE; 2 (2,6 DIMETHOXYPHENYL) 3 (4 METHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2,6 DIMETHOXYPHENYL) 3 (4,6 DIMETHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2,6 DIMETHOXYPHENYL) 3 (6 METHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2,6 DIMETHYLPHENYL) 3 (3 METHYLPHENYL) 1,3 THIAZOLIDIN 4 ONE; 2 (2,6 DIMETHYLPHENYL) 3 (4 METHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2,6 DIMETHYLPHENYL) 3 (4 METHYLPYRIMIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2,6 DIMETHYLPHENYL) 3 (4,6 DIMETHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (2,6 DIMETHYLPHENYL) 3 (6 METHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (3 CHLORO 2 FLUORO 6 TRIFLUOROMETHYLPHENYL) 3 (3 METHYLPHENYL) 1,3 THIAZOLIDIN 4 ONE; 2 (3 CHLORO 2 FLUORO 6 TRIFLUOROMETHYLPHENYL) 3 (4 METHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (3 CHLORO 2 FLUORO 6 TRIFLUOROMETHYLPHENYL) 3 (4,6 DIMETHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (3 CHLORO 2 FLUORO 6 TRIFLUOROMETHYLPHENYL) 3 (6 METHYLPYRIDIN 2 YL) 1,3 THIAZOLIDIN 4 ONE; 2 (FLUORO 6 METHOXYPHENYL) 3 (3 METHYLPHENYL) 1,3 THIAZOLIDIN 4 ONE; 3 (4,6 DIMETHYLPYRIDIN 2 YL) 2 (2 FLUORO 6 METHOXYPHENYL) 1,3 THIAZOLIDIN 4 ONE; 3 (6 BROMOPYRIDIN 2 YL) 2 (2 CHLORO 6 FLUORO 3 METHYLPHENYL) 1,3 THIAZOLIDIN 4 ONE; 3 (6 BROMOPYRIDIN 2 YL) 2 (2 FLUORO 6 METHOXYPHENYL) 1,3 THIAZOLIDIN 4 ONE; 3 (6 BROMOPYRIDIN 2 YL) 2 (2,6 DIMETHOXYPHENYL) 1,3 THIAZOLIDIN 4 ONE; 3 (6 BROMOPYRIDIN 2 YL) 2 (2,6 DIMETHYLPHENYL) 1,3 THIAZOLIDIN 4 ONE; 3 (6 BROMOPYRIDIN 2 YL) 2 (3 CHLORO 2 FLUORO 6 TRIFLUOROMETHYLPHENYL) 1,3 THIAZOLIDIN 4 ONE; ANTI HUMAN IMMUNODEFICIENCY VIRUS AGENT; RNA DIRECTED DNA POLYMERASE INHIBITOR; THIAZOLIDINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 1642538940     PISSN: 0014827X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.farmac.2003.09.001     Document Type: Article
Times cited : (97)

References (17)
  • 1
    • 0037130296 scopus 로고    scopus 로고
    • New development in anti-HIV chemotherapy
    • De Clercq E. New development in anti-HIV chemotherapy. Biochim. Biophys. Acta. 1587:2002;258-275.
    • (2002) Biochim. Biophys. Acta , vol.1587 , pp. 258-275
    • De Clercq, E.1
  • 2
    • 0028924567 scopus 로고
    • Mechanism of inhibition of reverse transcriptase by non-nucleoside inhibitors
    • Esnouf R., Ren J., Ross C., Jones Y., Stammers D., Stuart D. Mechanism of inhibition of reverse transcriptase by non-nucleoside inhibitors. Nat. Struct. Biol. 2:1995;303-308.
    • (1995) Nat. Struct. Biol. , vol.2 , pp. 303-308
    • Esnouf, R.1    Ren, J.2    Ross, C.3    Jones, Y.4    Stammers, D.5    Stuart, D.6
  • 3
    • 0033014605 scopus 로고    scopus 로고
    • Guide to major clinical trials in antiretroviral therapy in human immunodeficiency virus-infected patients: Protease inhibitors, non-nucleoside reverse transcriptase inhibitors, and nucleoside reverse transcriptase inhibitors
    • Tavel J.A., Miller K.D., Masur H. Guide to major clinical trials in antiretroviral therapy in human immunodeficiency virus-infected patients: protease inhibitors, non-nucleoside reverse transcriptase inhibitors, and nucleoside reverse transcriptase inhibitors. Clin. Inf. Dis. 28:1999;643-676.
    • (1999) Clin. Inf. Dis. , vol.28 , pp. 643-676
    • Tavel, J.A.1    Miller, K.D.2    Masur, H.3
  • 4
    • 2642709177 scopus 로고    scopus 로고
    • Declining morbidity and mortality among patients advanced human immunodeficiency virus infection. HIV outpatient study investigators
    • Palella F.J., Delaney K.M., Moorman A.C., Loveless M.O., Fuhrer J., Satten G.A., et al. Declining morbidity and mortality among patients advanced human immunodeficiency virus infection. HIV outpatient study investigators. New. Engl. J. Med. 338:1998;853-860.
    • (1998) New. Engl. J. Med. , vol.338 , pp. 853-860
    • Palella, F.J.1    Delaney, K.M.2    Moorman, A.C.3    Loveless, M.O.4    Fuhrer, J.5    Satten, G.A.6
  • 5
    • 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., et al. 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. Antiv. Chem. Chemother. 8:1997;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
  • 6
    • 17744407573 scopus 로고    scopus 로고
    • Synthesis, structure and in vitro anti-human immunodeficiency virus activity of novel 3-methyl-1H,3H-thiazolo[3,4-a]benzimidazoles
    • Chimirri A., Grasso S., Monforte A.M., Monforte P., Rao A., Zappalà M., et al. Synthesis, structure and in vitro anti-human immunodeficiency virus activity of novel 3-methyl-1H,3H-thiazolo[3,4-a] benzimidazoles. Antiv. Chem. Chemother. 9:1998;431-438.
    • (1998) Antiv. Chem. Chemother , vol.9 , pp. 431-438
    • Chimirri, A.1    Grasso, S.2    Monforte, A.M.3    Monforte, P.4    Rao, A.5    Zappalà, M.6
  • 7
    • 0032772910 scopus 로고    scopus 로고
    • Synthesis and biological activity of novel 1H,3H-thiazolo[3,4-a] benzimidazoles: Non-nucleoside human immunodeficiency virus type 1 reverse transcriptase inhibitors
    • Chimirri A., Grasso S., Monforte P., Rao A., Zappalà M., Monforte A.M., et al. Synthesis and biological activity of novel 1H,3H-thiazolo[3,4-a] benzimidazoles: non-nucleoside human immunodeficiency virus type 1 reverse transcriptase inhibitors. Antiv. Chem. Chemother. 10:1999;211-217.
    • (1999) Antiv. Chem. Chemother , vol.10 , pp. 211-217
    • Chimirri, A.1    Grasso, S.2    Monforte, P.3    Rao, A.4    Zappalà, M.5    Monforte, A.M.6
  • 9
    • 0036754669 scopus 로고    scopus 로고
    • Synthesis and anti-HIV activity of 2,3-diaryl-1,3-thiazolidin-4-(thi)one derivatives
    • Rao A., Carbone A., Chimirri A., De Clercq E., Monforte A.M., Monforte P., et al. Synthesis and anti-HIV activity of 2,3-diaryl-1,3-thiazolidin-4-(thi) one derivatives. Il Farmaco. 57:2002;747-751.
    • (2002) Il Farmaco , vol.57 , pp. 747-751
    • Rao, A.1    Carbone, A.2    Chimirri, A.3    De Clercq, E.4    Monforte, A.M.5    Monforte, P.6
  • 10
    • 0037153210 scopus 로고    scopus 로고
    • Design, synthesis, structure-activity relationships and molecular modeling studies of 2,3-diaryl-1,3-thiazolidin-4-ones as potent anti-HIV agents
    • Barreca M.L., Balzarini J., Chimirri A., De Clercq E., De Luca L., Höltje H.D., et al. Design, synthesis, structure-activity relationships and molecular modeling studies of 2,3-diaryl-1,3-thiazolidin-4-ones as potent anti-HIV agents. J. Med. Chem. 45:2002;5410-5413.
    • (2002) J. Med. Chem. , vol.45 , pp. 5410-5413
    • Barreca, M.L.1    Balzarini, J.2    Chimirri, A.3    De Clercq, E.4    De Luca, L.5    Höltje, H.D.6
  • 13
    • 0032744956 scopus 로고    scopus 로고
    • Novel modifications in the alkenyldiarylmethane (ADAM) series of non-nucleoside reverse transcriptase inhibitors
    • Casimiro-Garcia A., Micklatcher M., Turpin J.A., Stup T.L., Watson K., Buckheit R.W., et al. Novel modifications in the alkenyldiarylmethane (ADAM) series of non-nucleoside reverse transcriptase inhibitors. J. Med. Chem. 42:1999;4861-4874.
    • (1999) J. Med. Chem. , vol.42 , pp. 4861-4874
    • Casimiro-Garcia, A.1    Micklatcher, M.2    Turpin, J.A.3    Stup, T.L.4    Watson, K.5    Buckheit, R.W.6
  • 14
    • 0029075207 scopus 로고
    • Structure of HIV-1 RT/TIBO R 86183 complex reveals similarity in the binding of diverse nonnucleoside inhibitors
    • Ding J., Das K., Moereels H., Koymans L., Andries K., Janssen P.A.J., et al. Structure of HIV-1 RT/TIBO R 86183 complex reveals similarity in the binding of diverse nonnucleoside inhibitors. Nat. Struct. Biol. 2:1995;407-415.
    • (1995) Nat. Struct. Biol. , vol.2 , pp. 407-415
    • Ding, J.1    Das, K.2    Moereels, H.3    Koymans, L.4    Andries, K.5    Janssen, P.A.J.6
  • 15
    • 0023687234 scopus 로고
    • Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds
    • Pauwels R., Balzarini J., Baba M., Snoeck R., Schols D., Herdewijin P., et al. Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds. J. Virol. Method. 20:1988;309-321.
    • (1988) J. Virol. Method. , vol.20 , pp. 309-321
    • Pauwels, R.1    Balzarini, J.2    Baba, M.3    Snoeck, R.4    Schols, D.5    Herdewijin, P.6
  • 16
    • 0027328082 scopus 로고
    • HIV-1-specific reverse transcriptase inhibitors show differential activity against HIV-1 mutant strains containing different amino acid substitution in the reverse transcriptase
    • Balzarini J., Karlsson A., Pérez-Pérez M.-J., Vrang L., Walbers J., Zhang H., et al. HIV-1-specific reverse transcriptase inhibitors show differential activity against HIV-1 mutant strains containing different amino acid substitution in the reverse transcriptase. Virology. 192:1993;246-253.
    • (1993) Virology , vol.192 , pp. 246-253
    • Balzarini, J.1    Karlsson, A.2    Pérez-Pérez, M.-J.3    Vrang, L.4    Walbers, J.5    Zhang, H.6
  • 17
    • 0026724892 scopus 로고
    • Kinetics of inhibition of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase by the novel HIV-1-specific nucleoside analogue [2′,5′-bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl] -3′-spiro-5″-(4″-amino-1″,2″-oxathiole-2″, 2″-dioxide)thymine (TSAO-T)
    • Balzarini J., Pérez-Pérez M.-J., San-Félix A., Camarasa M.J., Bathurst I.C., Barr P.J., et al. Kinetics of inhibition of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase by the novel HIV-1-specific nucleoside analogue [2′,5′-bis-O-(tert- butyldimethylsilyl)-β-D-ribofuranosyl]-3′-spiro-5″-(4″- amino-1″,2″-oxathiole-2″,2″-dioxide)thymine (TSAO-T). J. Biol. Chem. 267:1992;11831-11838.
    • (1992) J. Biol. Chem. , vol.267 , pp. 11831-11838
    • Balzarini, J.1    Pérez-Pérez, M.-J.2    San-Félix, A.3    Camarasa, M.J.4    Bathurst, I.C.5    Barr, P.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.