ANTIVIRAL ACTIVITY;
ARTICLE;
CELL LINE;
CONTROLLED STUDY;
DRUG POTENCY;
DRUG SCREENING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
HUMAN IMMUNODEFICIENCY VIRUS;
NONHUMAN;
VIRUS STRAIN;
CHEMICAL STRUCTURE;
CHEMISTRY;
DRUG EFFECT;
HUMAN IMMUNODEFICIENCY VIRUS 1;
HUMAN IMMUNODEFICIENCY VIRUS 2;
LD 50;
STRUCTURE ACTIVITY RELATION;
SYNTHESIS;
VIRUS REPLICATION;
Anti-HIV agents II. Synthesis and in vitro anti-HIV activity of novel 1H,3H-thiazolo[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,3H-thiazolo[3,4-a]benzimidazoles. Farmaco. 46:1991;925-933.
Anti-HIV agents. IV. Synthesis and in vitro anti-HIV activity of novel 1-(2,6-difluorophenyl)-1H,3H-thiazolo[3,4-a]benzimidazoles
Chimirri A., Grasso S., Molica C., Monforte A.M., Monforte P., Zappalà M. Anti-HIV agents. IV. Synthesis and in vitro anti-HIV activity of novel 1-(2,6-difluorophenyl)-1H,3H-thiazolo[3,4-a]benzimidazoles. Farmaco. 51:1996;279-282.
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]benzimidazole, a potent non-nucleoside HIV-1 reverse transcriptase inhibitor. Antiviral 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., Bruno G., Nicolò F., Pannecouque C., Witvrouw M., De Clercq E. Synthesis, structure and in vitro anti-human immunodeficiency virus activity of novel 3-methyl-1H,3H-thiazolo[3,4-a]benzimidazoles. Antiviral 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., Pannecouque C., Witvrouw M., Balzarini J., De Clercq E. Synthesis and biological activity of novel 1H,3H-thiazolo[3,4-a]benzimidazoles: non-nucleoside human immunodeficiency virus type 1 reverse transcriptase inhibitors. Antiviral Chem. Chemother. 10:1999;211-217.
Comparative molecular field analysis (CoMFA) and docking studies of non-nucleoside HIV-1 RT inhibitors (NNRTIs)
Barreca M.L., Chimirri A., Carotti A., Carrieri A., Monforte A.M., Pellegrini Calace M., Rao A. Comparative molecular field analysis (CoMFA) and docking studies of non-nucleoside HIV-1 RT inhibitors (NNRTIs). Bioorg. Med. Chem. 7:1999;2283-2292.
Thiazolobenzimidazoles - A new class of anti-HIV agents
Schultz R.J., Bader J.P., Chimirri A., Covey J.M., Hill D.L., Haugwitz R.D., Guziec F.S., Narayanan V.L. Thiazolobenzimidazoles - a new class of anti-HIV agents. Proc. Am. Assoc. Cancer Res. 33:1992;517.
C,C- and C,N-linked dimers and 4-arylmethyl derivatives from 4-arylmethylene pyrazol-5-ones and isoxazol-5-ones with 2-arylbenzimidazolines
Risitano F., Grassi G., Caruso F., Foti F. C,C- and C,N-linked dimers and 4-arylmethyl derivatives from 4-arylmethylene pyrazol-5-ones and isoxazol-5-ones with 2-arylbenzimidazolines. Tetrahedron. 52:1996;1443-1450.
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., Desmyter J., De Clercq E. Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds. J. Virol. Methods. 20:1988;309-321.
Antiviral activity of low-MW dextran sulfate (derived from dextran MW 1000) compared to dextran sulfate samples of higher MW
Witvrouw M., Schols D., Andrei G., Snoeck R., Hosoya M., Pauwels R., Balzarini J., De Clercq E. Antiviral activity of low-MW dextran sulfate (derived from dextran MW 1000) compared to dextran sulfate samples of higher MW. Antiviral Chem. Chemother. 2:1991;171-179.