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Bis(heteroaryl)piperazine (BHAP) reverse transcriptase inhibitors: structure-activity relationships of novel substituted indole analogues and the identification of 1-[(5-methanesulfonamido-1H-indol-2-yl)-carbonyl]-4-[3- [(1-methylethyl)amino]-pyridinyl]piperazine monomethanesulfonate (U-90152S), a second-generation clinical candidate

Journal of medicinal chemistry, 1993-05, Vol.36 (10), p.1505-1508

1993

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Targeting Delavirdine/Atevirdine Resistant HIV-1: Identification of (Alkylamino)piperidine-Containing Bis(heteroaryl)piperazines as Broad Spectrum HIV-1 Reverse Transcriptase Inhibitors

Journal of medicinal chemistry, 1996-09, Vol.39 (19), p.3769-3789

1996

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(Alkylamino) piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes

Journal of Virology, 1996-06, Vol.70 (6), p.3698-3705

1996

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The occurrence of 13,14-dihydro and 13,14-cis-unsaturated prostaglandins in the coral, Plexaura homomalla. Synthesis of 13,14-cis-prostaglandin E2, 15-acetate methyl ester, and the 13,14-cis analogs of prostaglandin F2.alpha. and prostaglandin F2.beta

Journal of the American Chemical Society, 1977-08, Vol.99 (18), p.6062-6066

1977

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Discovery, Synthesis, and Bioactivity of Bis(heteroaryl)piperazines. 1. A Novel Class of Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors

Journal of medicinal chemistry, 1994-04, Vol.37 (7), p.999-1014

1994

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(Alkylamino)piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1 sub(IIIB) with reduced replication phenotypes

Journal of virology, 1996-01, Vol.70 (6), p.3698-3705

1996

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Bis(heteroaryl)piperazine (BHAP) reverse transcriptase inhitors : structure-activity relationships of novel substituted indole analogues and the identification of 1-[(5-methanesulfonamido-1-H-indol-2-yl)-carbonyl]-4-[3-[(1-methylethyl)amino]-pyridinyl]piperazine monomethanesulfonate (U-90152S), a second-generation clinical candidate

Journal of medicinal chemistry, 1993, Vol.36 (10), p.1505-1508

1993

Volltextzugriff (PDF)

Bis(heteroaryl)piperazine (BHAP) reverse transcriptase inhibitors: Structure-activity relationships of novel substituted indole analogues and the identification of 1-((5-methanesulfonamido-1H-indol-2-yl)-carbonyl)-4-(3-((1-methyle thyl)amino)-pyridinyl)piperazine monomethanesulfonate (U-90152S), a second-generation clinical candidate

Journal of medicinal chemistry, 1993-01, Vol.36 (10), p.1505-1508

1993

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Discovery, synthesis, and bioactivity of bis(heteroaryl)piperazines. I: A novel class of non-nucleoside HIV-1 reverse transcriptase inhibitors

Journal of medicinal chemistry, 1994, Vol.37 (7), p.999-1014

1994

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Spectroscopic studies of delavirdine mesylate (U-90,152T) a bis(heteroaryl)piperazine (BHAP) HIV reverse transcriptase inhibitor

Journal of heterocyclic chemistry, 1996-03, Vol.33 (2), p.493-496

1996

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ChemInform Abstract: Reaction of 2‐(Alkylsulfinyl)‐, 2‐(Arylsulfinyl)‐, and 2‐(Aralkylsulfinyl)benzimidazoles with Thiols: A Convenient Synthesis of Unsymmetrical Disulfides

ChemInform, 1988-03, Vol.19 (11), p.no-no

1988

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Facile ring cleavage of prostaglandin epoxy ketones

Journal of organic chemistry, 1978-02, Vol.43 (4), p.759-760

1978

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ChemInform Abstract: Discovery, Synthesis, and Bioactivity of Bis(heteroaryl)piperazines. Part 1. A Novel Class of Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors

ChemInform, 1994-08, Vol.25 (34), p.no-no

1994

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Structure-Based Design of HIV Protease Inhibitors: 5,6-Dihydro-4-hydroxy-2-pyrones as Effective, Nonpeptidic Inhibitors

Journal of medicinal chemistry, 1996-11, Vol.39 (23), p.4630-4642

1996

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Perceived vs. Actual Distance to Transit in Santiago, Chile

Journal of public transportation, 2015-01, Vol.18 (4), p.16-30

2015

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take time for action: Step Up to Nonlinear Functions

Mathematics teaching in the middle school, 2010-02, Vol.15 (6), p.310-313

2010

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Reaction of 2-(alkylsulfinyl)-, 2-(arylsulfinyl)-, and 2-(aralkylsulfinyl)benzimidazoles with thiols: a convenient synthesis of unsymmetrical disulfides

Journal of organic chemistry, 1987-10, Vol.52 (20), p.4620-4622

1987

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Total synthesis of 3-oxa-4,5,6-trinor-3,7-inter-m-phenylene prostaglandins. 1. Photochemical approach

Journal of organic chemistry, 1978-05, Vol.43 (11), p.2093-2101

1978

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Epidermal Structure and Ontogeny of Stomata in Some Centrospermae

Feddes repertorium, 1977-10, Vol.88 (7-8), p.465-475

1977

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Epidermal Structure and Ontogeny of Stomata in Some Centrospermae

Feddes repertorium, 1977, Vol.88 (7-8), p.465-475

1977

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New Horizons in Evolution

1, 2021

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Targeting Delavirdine/Atevirdine Resistant HIV-1: Identification of (Alkylamino)piperidine-Containing Bis(heteroaryl)piperazines as Broad Spectrum HIV-1 Reverse Transcriptase Inhibitors

(Alkylamino) piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1IIIB with reduced replication phenotypes

The occurrence of 13,14-dihydro and 13,14-cis-unsaturated prostaglandins in the coral, Plexaura homomalla. Synthesis of 13,14-cis-prostaglandin E2, 15-acetate methyl ester, and the 13,14-cis analogs of prostaglandin F2.alpha. and prostaglandin F2.beta

Discovery, Synthesis, and Bioactivity of Bis(heteroaryl)piperazines. 1. A Novel Class of Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors

(Alkylamino)piperidine bis(heteroaryl)piperizine analogs are potent, broad-spectrum nonnucleoside reverse transcriptase inhibitors of drug-resistant isolates of human immunodeficiency virus type 1 (HIV-1) and select for drug-resistant variants of HIV-1 sub(IIIB) with reduced replication phenotypes

Discovery, synthesis, and bioactivity of bis(heteroaryl)piperazines. I: A novel class of non-nucleoside HIV-1 reverse transcriptase inhibitors

Spectroscopic studies of delavirdine mesylate (U-90,152T) a bis(heteroaryl)piperazine (BHAP) HIV reverse transcriptase inhibitor

ChemInform Abstract: Reaction of 2‐(Alkylsulfinyl)‐, 2‐(Arylsulfinyl)‐, and 2‐(Aralkylsulfinyl)benzimidazoles with Thiols: A Convenient Synthesis of Unsymmetrical Disulfides

Facile ring cleavage of prostaglandin epoxy ketones

ChemInform Abstract: Discovery, Synthesis, and Bioactivity of Bis(heteroaryl)piperazines. Part 1. A Novel Class of Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors

Structure-Based Design of HIV Protease Inhibitors: 5,6-Dihydro-4-hydroxy-2-pyrones as Effective, Nonpeptidic Inhibitors

Perceived vs. Actual Distance to Transit in Santiago, Chile

take time for action: Step Up to Nonlinear Functions

Reaction of 2-(alkylsulfinyl)-, 2-(arylsulfinyl)-, and 2-(aralkylsulfinyl)benzimidazoles with thiols: a convenient synthesis of unsymmetrical disulfides

Total synthesis of 3-oxa-4,5,6-trinor-3,7-inter-m-phenylene prostaglandins. 1. Photochemical approach

Epidermal Structure and Ontogeny of Stomata in Some Centrospermae

Epidermal Structure and Ontogeny of Stomata in Some Centrospermae

New Horizons in Evolution

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