Inhibition of human immunodeficiency virus integrase by bis-catechols - Wikidata - wikimedia - TriplyDB

Inhibition of human immunodeficiency virus integrase by bis-catechols

Inhibition of human immunodeficiency virus integrase by bis-catechols

http://www.wikidata.org/entity/Q28368086

about

A historical sketch of the discovery and development of HIV-1 integrase inhibitors Resistance to the anti-human immunodeficiency virus type 1 compound L-chicoric acid results from a single mutation at amino acid 140 of integrase Human immunodeficiency virus type 1 cDNA integration: new aromatic hydroxylated inhibitors and studies of the inhibition mechanism.Isolation and characterization of novel human immunodeficiency virus integrase inhibitors from fungal metabolites Identification of a hexapeptide inhibitor of the human immunodeficiency virus integrase protein by using a combinatorial chemical library Inhibitors of HIV-1 replication [corrected; erratum to be published] that inhibit HIV integrase Differential inhibition of HIV-1 preintegration complexes and purified integrase protein by small molecules Dicaffeoylquinic and dicaffeoyltartaric acids are selective inhibitors of human immunodeficiency virus type 1 integrase.Equivalent inhibition of half-site and full-site retroviral strand transfer reactions by structurally diverse compounds Inhibition of acute-, latent-, and chronic-phase human immunodeficiency virus type 1 (HIV-1) replication by a bistriazoloacridone analog that selectively inhibits HIV-1 transcription Diarylsulfones, a novel class of human immunodeficiency virus type 1 integrase inhibitors Nucleophile selection for the endonuclease activities of human, ovine, and avian retroviral integrases.Irreversible inhibition of human immunodeficiency virus type 1 integrase by dicaffeoylquinic acids.Efficiency and fidelity of full-site integration reactions using recombinant simian immunodeficiency virus integrase Current developments in HIV chemotherapy.HIV integrase inhibitors as therapeutic agents in AIDS.HIV-1 integrase inhibitors: a review of their chemical development.Alternate strand DNA triple helix-mediated inhibition of HIV-1 U5 long terminal repeat integration in vitro.Effects of mutations in residues near the active site of human immunodeficiency virus type 1 integrase on specific enzyme-substrate interactions.Differential divalent cation requirements uncouple the assembly and catalytic reactions of human immunodeficiency virus type 1 integrase.Design and synthesis of novel dihydroxyindole-2-carboxylic acids as HIV-1 integrase inhibitors.Synthesis and anti-human immunodeficiency virus type 1 integrase activity of hydroxybenzoic and hydroxycinnamic acid flavon-3-yl esters.Structure-Guided Optimization of HIV Integrase Strand Transfer Inhibitors.Tricyclic flavonoids with 1,3-dithiolium substructure.

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Inhibition of human immunodeficiency virus integrase by bis-catechols

http://www.wikidata.org/entity/Q28368086

description

1995 nî lūn-bûn

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1995 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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1995 թվականի փետրվարին հրատարակված գիտական հոդված

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1995年の論文

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1995年論文

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1995年論文

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1995年論文

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1995年論文

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1995年論文

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1995年论文

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name

Inhibition of human immunodeficiency virus integrase by bis-catechols

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Inhibition of human immunodeficiency virus integrase by bis-catechols

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Inhibition of human immunodeficiency virus integrase by bis-catechols

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Inhibition of human immunodeficiency virus integrase by bis-catechols

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Inhibition of human immunodeficiency virus integrase by bis-catechols

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Inhibition of human immunodeficiency virus integrase by bis-catechols

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Inhibition of human immunodeficiency virus integrase by bis-catechols

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Inhibition of human immunodeficiency virus integrase by bis-catechols

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Inhibition of human immunodeficiency virus integrase by bis-catechols

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Antimicrobial Agents and Chemotherapy

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Inhibition of human immunodeficiency virus integrase by bis-catechols

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A Wolfe

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D J Hazuda

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E A Emini

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J C Hastings

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K LeGrow

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P L Graham

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R L LaFemina

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S D Young

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P2860

Functional analysis of HIV-1 reverse transcriptase amino acids involved in resistance to multiple nonnucleoside inhibitors

Inhibition of HIV-1 integration protein by aurintricarboxylic acid monomers, monomer analogs, and polymer fractions

Synthesis and anti-HIV activities of low molecular weight aurintricarboxylic acid fragments and related compounds

Inhibition of cap (m7GpppXm)-dependent endonuclease of influenza virus by 4-substituted 2,4-dioxobutanoic acid compounds

Inhibitors of human immunodeficiency virus integrase

Retroviral DNA integration directed by HIV integration protein in vitro

Retroviral integration: structure of the initial covalent product and its precursor, and a role for the viral IN protein

Association of integrase, matrix, and reverse transcriptase antigens of human immunodeficiency virus type 1 with viral nucleic acids following acute infection

Human immunodeficiency virus integration protein expressed in Escherichia coli possesses selective DNA cleaving activity

Both substrate and target oligonucleotide sequences affect in vitro integration mediated by human immunodeficiency virus type 1 integrase protein produced in Saccharomyces cerevisiae.

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320-4

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scholarly article

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10.1128/AAC.39.2.320

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2

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39

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1995-02-01T00:00:00Z

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15471677

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7726489

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162534

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