Search Results - "Buckheit, R W"
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Preclinical evaluation of a mercaptobenzamide and its prodrug for NCp7-targeted inhibition of human immunodeficiency virus
Published in Antiviral research (01-10-2016)“…Although the effective use of highly active antiretroviral therapy results in the suppression of virus production in infected individuals, it does not…”
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Synthesis and Biological Activity of Novel Nonnucleoside Inhibitors of HIV-1 Reverse Transcriptase. 2-Aryl-Substituted Benzimidazoles
Published in Journal of medicinal chemistry (19-12-1997)“…The development of new nonnucleoside inhibitors of human immunodeficiency virus type-1 (HIV-1) reverse transcriptase (RT) active against the drug-induced…”
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3
Vaginal film for prevention of HIV: using visual and tactile evaluations among potential users to inform product design
Published in Pharmaceutical development and technology (16-03-2018)“…Topical prevention of HIV and other STIs is a global health priority. To provide options for users, developers have worked to design safe, effective and…”
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Discovery of cyanovirin-N, a novel human immunodeficiency virus-inactivating protein that binds viral surface envelope glycoprotein gp120: potential applications to microbicide development
Published in Antimicrobial Agents and Chemotherapy (01-07-1997)“…Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon…”
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Combinatorially Selected Guanosine-Quartet Structure is a Potent Inhibitor of Human Immunodeficiency Virus Envelope-Mediated Cell Fusion
Published in Proceedings of the National Academy of Sciences - PNAS (15-02-1994)“…The phosphorothioate oligonucleotide T2G4T2was identified as an inhibitor of HIV infection in vitro by combinatorial screening of a library of phosphorothioate…”
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The calanolides, a novel HIV-inhibitory class of Coumarin derivatives from the tropical rainforest tree, Calophyllum lanigerum
Published in Journal of medicinal chemistry (24-07-1992)“…Eight new coumarin compounds (1-8) were isolated by anti-HIV bioassay-guided fractionation of an extract of Calophyllum lanigerum. The structures of calanolide…”
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Inhibitors of HIV Nucleocapsid Protein Zinc Fingers as Candidates for the Treatment of AIDS
Published in Science (American Association for the Advancement of Science) (17-11-1995)“…Strategies for the treatment of human immunodeficiency virus-type 1 (HIV-1) infection must contend with the obstacle of drug resistance. HIV-1 nucleocapsid…”
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Michellamine B, a novel plant alkaloid, inhibits human immunodeficiency virus-induced cell killing by at least two distinct mechanisms
Published in Antimicrobial Agents and Chemotherapy (01-02-1995)“…Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon…”
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Inhibition of multiple phases of human immunodeficiency virus type 1 replication by a dithiane compound that attacks the conserved zinc fingers of retroviral nucleocapsid proteins
Published in Antimicrobial Agents and Chemotherapy (01-02-1997)“…Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon…”
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Inhibition of in Vitro and in Vivo HIV Replication by a Distamycin Analogue That Interferes with Chemokine Receptor Function: A Candidate for Chemotherapeutic and Microbicidal Application
Published in Journal of medicinal chemistry (18-06-1998)“…Select chemokine receptors act as coreceptors for HIV-1 entry into human cells and represent targets for antiviral therapy. In this report we describe a…”
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Anti-HIV michellamines from Ancistrocladus korupensis
Published in Journal of medicinal chemistry (10-06-1994)“…Here we report details of the isolation and determination of the absolute configurations and comparative anti-HIV activities of novel, atropisomeric…”
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Diarylsulfones, a new chemical class of nonnucleoside antiviral inhibitors of human immunodeficiency virus type 1 reverse transcriptase
Published in Antimicrobial Agents and Chemotherapy (01-04-1993)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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Unique Anti-Human Immunodeficiency Virus Activities of the Nonnucleoside Reverse Transcriptase Inhibitors Calanolide A, Costatolide, and Dihydrocostatolide
Published in Antimicrobial Agents and Chemotherapy (01-08-1999)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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T30177, an oligonucleotide stabilized by an intramolecular guanosine octet, is a potent inhibitor of laboratory strains and clinical isolates of human immunodeficiency virus type 1
Published in Antimicrobial Agents and Chemotherapy (01-11-1995)“…Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon…”
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15
Structure-activity and cross-resistance evaluations of a series of human immunodeficiency virus type-1-specific compounds related to oxathiin carboxanilide
Published in Antimicrobial Agents and Chemotherapy (01-12-1995)“…Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon…”
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Structural Analogues of the Calanolide Anti-HIV Agents. Modification of the trans-10,11-Dimethyldihydropyran-12-ol Ring (Ring C)
Published in Journal of medicinal chemistry (14-03-1997)“…(+)-Calanolide A is a potent inhibitor of reverse transcriptase from human immunodeficiency virus type 1 (HIV-1), which was isolated from an extract of…”
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The Biological Effects of Structural Variation at the Meta Position of the Aromatic Rings and at the End of the Alkenyl Chain in the Alkenyldiarylmethane Series of Non-Nucleoside Reverse Transcriptase Inhibitors
Published in Journal of medicinal chemistry (22-11-2001)“…In an effort to elucidate a set of structure−activity relationships in the alkenyldiarylmethane (ADAM) series of non-nucleoside reverse transcriptase…”
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Antiviral activity and mechanism of action of calanolide A against the human immunodeficiency virus type-1
Published in The Journal of pharmacology and experimental therapeutics (01-11-1996)“…Calanolide A, recently discovered in extracts from the tropical rainforest tree, Calophyllum lanigerum, is a novel inhibitor of the human immunodeficiency…”
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Evaluation of Selected Chemotypes in Coupled Cellular and Molecular Target-Based Screens Identifies Novel HIV-1 Zinc Finger Inhibitors
Published in Journal of medicinal chemistry (13-09-1996)“…Conservation of the Cys-Xaa2-Cys-Xaa4-His-Xaa4-Cys retroviral zinc finger sequences and their absolute requirement in both the early and late phases of…”
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Mechanism of inhibition of human immunodeficiency virus type 1 reverse transcriptase and human DNA polymerases alpha, beta, and gamma by the 5'-triphosphates of carbovir, 3'-azido-3'-deoxythymidine, 2',3'-dideoxyguanosine and 3'-deoxythymidine. A novel RNA template for the evaluation of antiretroviral drugs
Published in The Journal of biological chemistry (25-01-1991)“…Carbovir (the carbocyclic analog of 2'-3'-didehydro-2',3'-dideoxyguanosine) is a potent inhibitor of human immunodeficiency virus type 1 (HIV-1) replication…”
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