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Inhibitors of human immunodeficiency virus integrase

Inhibitors of human immunodeficiency virus integrase

http://www.wikidata.org/entity/Q28378683

about

The site of antiviral action of 3-nitrosobenzamide on the infectivity process of human immunodeficiency virus in human lymphocytes First-in-class small molecule inhibitors of the single-strand DNA cytosine deaminase APOBEC3G Caffeic acid phenethyl ester is a potent and specific inhibitor of activation of nuclear transcription factor NF-kappa B Antiviral properties of caffeic acid phenethyl ester and its potential application A historical sketch of the discovery and development of HIV-1 integrase inhibitors Specific inhibition of human immunodeficiency virus type 1 (HIV-1) integration in cell culture: putative inhibitors of HIV-1 integrase Inhibition of human immunodeficiency virus integrase by bis-catechols 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.Inhibition of human immunodeficiency virus type 1 integrase by 3'-azido-3'-deoxythymidylate 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 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 NP-06: a novel anti-human immunodeficiency virus polypeptide produced by a Streptomyces species 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 Inhibitory effects of caffeic acid phenethyl ester derivatives on replication of hepatitis C virus Caffeic Acid phenethyl ester protects blood-brain barrier integrity and reduces contusion volume in rodent models of traumatic brain injury.Novel paradigms for drug discovery: computational multitarget screening Bee products prevent VEGF-induced angiogenesis in human umbilical vein endothelial cells Irreversible inhibition of human immunodeficiency virus type 1 integrase by dicaffeoylquinic acids.Plant products as antimicrobial agents.HIV-1 IN inhibitors: 2010 update and perspectives Biochemical and pharmacological analyses of HIV-1 integrase flexible loop mutants resistant to raltegravir Resistance to integrase inhibitors.Incorporation of a fluorescent guanosine analog into oligonucleotides and its application to a real time assay for the HIV-1 integrase 3'-processing reaction HIV-1 integrase and RNase H activities as therapeutic targets.Targeting HIV-1 integrase.Role of raltegravir in the management of HIV-1 infection.Authentic HIV-1 integrase inhibitors.Inhibition of HIV Expression and Integration in Macrophages by Methylglyoxal-Bis-Guanylhydrazone.Detection and characterization of a functional complex of human immunodeficiency virus type 1 integrase and its DNA substrate by UV cross-linking.Rapid solution assays for retroviral integration reactions and their use in kinetic analyses of wild-type and mutant Rous sarcoma virus integrases Role of integrase inhibitors in the treatment of HIV disease.Phytoestrogens: perpetrators or protectors?Azido-containing diketo acid derivatives inhibit human immunodeficiency virus type 1 integrase in vivo and influence the frequency of deletions at two-long-terminal-repeat-circle junctions.Novel bifunctional quinolonyl diketo acid derivatives as HIV-1 integrase inhibitors: design, synthesis, biological activities, and mechanism of action Novel quinolinonyl diketo acid derivatives as HIV-1 integrase inhibitors: design, synthesis, and biological activities

P2860

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P2860

Inhibitors of human immunodeficiency virus integrase

http://www.wikidata.org/entity/Q28378683

description

1993 nî lūn-bûn

@nan

1993 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

1993 թվականի մարտին հրատարակված գիտական հոդված

@hy

1993年の論文

@ja

1993年論文

@yue

1993年論文

@zh-hant

1993年論文

@zh-hk

1993年論文

@zh-mo

1993年論文

@zh-tw

1993年论文

@wuu

name

Inhibitors of human immunodeficiency virus integrase

@ast

Inhibitors of human immunodeficiency virus integrase

@en

Inhibitors of human immunodeficiency virus integrase

@nl

type

label

Inhibitors of human immunodeficiency virus integrase

@ast

Inhibitors of human immunodeficiency virus integrase

@en

Inhibitors of human immunodeficiency virus integrase

@nl

prefLabel

Inhibitors of human immunodeficiency virus integrase

@ast

Inhibitors of human immunodeficiency virus integrase

@en

Inhibitors of human immunodeficiency virus integrase

@nl

P1433

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P1476

Q28378683-0F3157BE-06E1-4840-A7D2-134B2657C786

P2093

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P2860

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P304

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P31

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P3181

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P356

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P5875

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P932

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P3181

P356

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Inhibitors of human immunodeficiency virus integrase

@en

P2093

F Leteurtre

http://www.w3.org/2001/XMLSchema#string

K W Kohn

http://www.w3.org/2001/XMLSchema#string

M R Fesen

http://www.w3.org/2001/XMLSchema#string

Y Pommier

http://www.w3.org/2001/XMLSchema#string

P2860

Thermodynamics of the interactions of m-AMSA and o-AMSA with nucleic acids: influence of ionic strength and DNA base composition

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

Inhibition of human immunodeficiency virus (HIV-1) replication in vitro by noncytotoxic doses of camptothecin, a topoisomerase I inhibitor

Retroviral DNA integration directed by HIV integration protein in vitro

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.

Antitumor activity, pharmacology, and toxicity of ellipticines, ellipticinium, and 9-hydroxy derivatives: preliminary clinical trials of 2-methyl-9-hydroxy ellipticinium (NSC 264-137).

DNA unwinding and inhibition of mouse leukemia L1210 DNA topoisomerase I by intercalators.

A rapid in vitro assay for HIV DNA integration.

Local base sequence preferences for DNA cleavage by mammalian topoisomerase II in the presence of amsacrine or teniposide.

P304

2399-403

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P31

scholarly article

P3181

4656247

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P356

10.1073/PNAS.90.6.2399

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P407

P433

6

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P478

90

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P577

1993-03-15T00:00:00Z

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P5875

14739462

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P698

8460151

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P932

46094

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