Retroviral integrase inhibitors year 2000: update and perspectives (Q33916746)

30 July 2017

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title

Retroviral integrase inhibitors year 2000: update and perspectives (English)

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30 July 2017

Pommier Y

1

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30 July 2017

Marchand C

series ordinal

2

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30 July 2017

Neamati N

series ordinal

3

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30 July 2017

publication date

1 September 2000

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30 July 2017

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30 July 2017

volume

47

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30 July 2017

issue

3

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30 July 2017

page(s)

139-148

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The plant ribosome inactivating proteins luffin and saporin are potent inhibitors of HIV-1 integrase

30 July 2017

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Sequence specificity of viral end DNA binding by HIV-1 integrase reveals critical regions for protein-DNA interaction

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Inhibition of HIV-1 integrase by flavones, caffeic acid phenethyl ester (CAPE) and related compounds

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Linked lexitropsins and the in vitro inhibition of HIV-1 reverse transcriptase RNA-directed DNA polymerization: a novel induced-fit of 3,5 m-pyridyl bisdistamycin to enzyme-associated template-primer

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Structure of the HIV-1 integrase catalytic domain complexed with an inhibitor: a platform for antiviral drug design

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Differential divalent cation requirements uncouple the assembly and catalytic reactions of human immunodeficiency virus type 1 integrase.

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7 January 2021

Isolation and characterization of novel human immunodeficiency virus integrase inhibitors from fungal metabolites

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7 January 2021

Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells

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7 January 2021

Mechanism of inhibition of HIV-1 integrase by G-tetrad-forming oligonucleotides in Vitro

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Stability-activity relationships of a family of G-tetrad forming oligonucleotides as potent HIV inhibitors. A basis for anti-HIV drug design

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Resistance to the anti-human immunodeficiency virus type 1 compound L-chicoric acid results from a single mutation at amino acid 140 of integrase

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Structure-activity relationships: analogues of the dicaffeoylquinic and dicaffeoyltartaric acids as potent inhibitors of human immunodeficiency virus type 1 integrase and replication

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7 January 2021

Chicoric acid analogues as HIV-1 integrase inhibitors

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7 January 2021

Structure of the catalytic domain of avian sarcoma virus integrase with a bound HIV-1 integrase-targeted inhibitor

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7 January 2021

Antiretroviral agents as inhibitors of both human immunodeficiency virus type 1 integrase and protease.

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7 January 2021

Styrylquinoline derivatives: a new class of potent HIV-1 integrase inhibitors that block HIV-1 replication in CEM cells

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7 January 2021

Depsides and depsidones as inhibitors of HIV-1 integrase: discovery of novel inhibitors through 3D database searching.

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7 January 2021

Potent inhibitors of human immunodeficiency virus type 1 integrase: identification of a novel four-point pharmacophore and tetracyclines as novel inhibitors.

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7 January 2021

Salicylhydrazine-containing inhibitors of HIV-1 integrase: implication for a selective chelation in the integrase active site

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7 January 2021

Thiazolothiazepine inhibitors of HIV-1 integrase

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7 January 2021

HIV-1 integrase inhibitors: past, present, and future

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7 January 2021

HIV-1 integrase pharmacophore: discovery of inhibitors through three-dimensional database searching

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7 January 2021

Selection of amino acid substitutions restoring activity of HIV-1 integrase mutated in its catalytic site using the yeast Saccharomyces cerevisiae

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7 January 2021

4 Viral entry as the primary target of anti-HIV activity of chicoric acid and its tetra-acetyl esters

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7 January 2021

Inhibitors of human immunodeficiency virus integrase.

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7 January 2021

Lamellarin alpha 20-sulfate, an inhibitor of HIV-1 integrase active against HIV-1 virus in cell culture

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7 January 2021

Synthetic DNA minor groove-binding drugs

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7 January 2021

L-chicoric acid, an inhibitor of human immunodeficiency virus type 1 (HIV-1) integrase, improves on the in vitro anti-HIV-1 effect of Zidovudine plus a protease inhibitor (AG1350).

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7 January 2021

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7 January 2021

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7 January 2021

Disruption of IRS-2 causes type 2 diabetes in mice

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7 January 2021

Crystal structure of an active two-domain derivative of Rous sarcoma virus integrase

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7 January 2021

Inhibition of HIV integrase by novel nucleotides bearing tricyclic bases

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7 January 2021

Irreversible inhibition of human immunodeficiency virus type 1 integrase by dicaffeoylquinic acids

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7 January 2021

Structure-activity relationships and binding mode of styrylquinolines as potent inhibitors of HIV-1 integrase and replication of HIV-1 in cell culture

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7 January 2021

10.1016/S0166-3542(00)00112-1

Identifiers

DOI

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30 July 2017

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