ARTICLE;
CONCENTRATION RESPONSE;
CONTROLLED STUDY;
DRUG CYTOTOXICITY;
DRUG EFFICACY;
DRUG SCREENING;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
IN VITRO STUDY;
VIRUS INHIBITION;
VIRUS REPLICATION;
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.
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.
Declining morbidity and mortality among patients advanced human immunodeficiency virus infection. HIV outpatient study investigators
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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.
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.
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.
Discovery of 2,3-diaryl-1,3-thiazolidin-4-ones as potent anti-HIV-1 agents
Barreca M.L., Chimirri A., De Luca L., Monforte A.M., Monforte P., Rao A., et al. Discovery of 2,3-diaryl-1,3-thiazolidin-4-ones as potent anti-HIV-1 agents. Bioorg. Med. Chem. Lett. 11:2001;1793-1796.
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.
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.
Synthesis and anti-HIV activity of 2,3-diaryl-1,3-thiazolidin-4-ones
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-ones. Il Farmaco. 58:2003;115-120.
A. Rao, J. Balzarini, A. Carbone, A. Chimirri, E. De Clercq, A.M. Monforte, et al., 2-(2,6-Dihalophenyl)-3-(pyrimidin-2-yl)-1,3-thiazolidin-4- ones as non-nucleoside HIV-1 reverse transcriptase inhibitors, submitted for publication.
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.
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.
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.
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.
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.