5 H-pyrrolo[1,2- b][1,2,5]benzothiadiazepines (PBTDs): A novel class of non-nucleoside reverse transcriptase inhibitors (original) (raw)

Pyrrolobenzothiazepinones and Pyrrolobenzoxazepinones: Novel and Specific Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors with Antiviral Activity

Giovanni Greco

Journal of Medicinal Chemistry, 1996

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2'5'-Bis-O-(tert-Butyldimethylsilyl)-3'Spiro5''- (4''Amino 1'',2''-Oxathiole-2'',2''Dioxide)Pyrimidine (TSAO) Nucleoside Analogues: Highly Selective Inhibitors of Human Immunodeficiency Virus Type 1 that are Targeted at the Viral Reverse Transcriptase

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1-Arylsulfonyl-3-([alpha]-hydroxybenzyl)-1H-pyrroles, a novel class of anti-HIV-1 reverse transcriptase inhibitors

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Pyridinone derivatives: specific human immunodeficiency virus type 1 reverse transcriptase inhibitors with antiviral activity

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Design and anti-HIV activity of arylsulphonamides as non-nucleoside reverse transcriptase inhibitors

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[2',5'-Bis-O-(tert-butyldimethylsilyl)]-3'-spiro-5''-(4''-amino-1'',2''-oxathiole-2'',2''-dioxide) (TSAO) derivatives of purine and pyrimidinenucleosides as potent and selective inhibitors of human immunodeficiency virus type 1

María-josé Camarasa, Dominique Schols

Antimicrobial Agents and Chemotherapy, 1992

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An antiviral target on reverse transcriptase of human immunodeficiency virus type 1 revealed by tetrahydroimidazo-[4,5,1-jk] [1,4]benzodiazepin-2 (1H)-one and -thione derivatives

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Novel 8-Substituted Dipyridodiazepinone Inhibitors with a Broad-Spectrum of Activity against HIV-1 Strains Resistant to Non-nucleoside Reverse Transcriptase Inhibitors

Robert Deziel

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N1-Alkyl pyrimidinediones as non-nucleoside inhibitors of HIV-1 reverse transcriptase

Jianhong Wang

Bioorganic & Medicinal Chemistry Letters, 2010

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Imidazo[1,2-a]pyridin-3-amines as potential HIV-1 non-nucleoside reverse transcriptase inhibitors

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Synthesis, Biological Activity, and Crystal Structure of Potent Nonnucleoside Inhibitors of HIV-1 Reverse Transcriptase That Retain Activity against Mutant Forms of the Enzyme †

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Inhibition of Human Immunodeficiency Virus by a New Class of Pyridine Oxide Derivatives

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Inhibitory activity of 9-phenylcyclohepta[d]pyrimidinedione derivatives against different strains of HIV-1 as non-nucleoside reverse transcriptase inhibitors

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2', 5'-Bis-O-(Tert-Butyldimethylsilyl)-3'-Spiro-5''-(4''-Amino-1'', 2''-Oxathiole-2'', 2'-Dioxide) Pyrimidine (TSAO) Nucleoside Analogues: Highlyselective Inhibitors of Human …

Ana San Felix

Proceedings of the …, 1992

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Computer-assisted design, synthesis and biological evaluation of novel pyrrolyl heteroaryl sulfones targeted at HIV-1 reverse transcriptase as non-nucleoside …

Antonio Lavecchia

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Identification of benzofurano[3,2-d]pyrimidin-2-ones, a new series of HIV-1 nucleotide-competing reverse transcriptase inhibitors

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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)-beta-D-ribofuranosyl]-3'-spiro-5 "- (4"-amino-1",2"-oxathiole-2",2"-dioxide)thymine (TSAO-T)

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The Journal of biological chemistry, 1992

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5Alkyl2-alkylamino-6-(2,6-difluorophenylalkyl)-3,4-dihydropyrimidin-4(3 H)-ones, a new series of potent, broad-spectrum non-nucleoside reverse transcriptase inhibitors belonging to the DABO family

Gianluca SBARDELLA

Bioorganic & Medicinal Chemistry, 2005

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Indoles and pyridazino[4,5- b]indoles as nonnucleoside analog inhibitors of HIV1 reverse transcriptase

Elisabet Santiago

European Journal of Medicinal Chemistry, 1995

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ChemInform Abstract: Synthesis and anti-HIV-1 Evaluation of 1,5-Disubstituted Pyrimidine-2,4-diones

Gabriella Collu

ChemInform, 2008

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