Improved guanide compounds which bind the CXCR4 co-receptor and inhibit HIV-1 infection

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http://www.wikidata.org/entity/Q36760742

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2013 nî lūn-bûn

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2013年の論文

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2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

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2013年论文

@zh

2013年论文

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name

Improved guanide compounds which bind the CXCR4 co-receptor and inhibit HIV-1 infection

@ast

Improved guanide compounds which bind the CXCR4 co-receptor and inhibit HIV-1 infection

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type

Item

label

Improved guanide compounds which bind the CXCR4 co-receptor and inhibit HIV-1 infection

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Improved guanide compounds which bind the CXCR4 co-receptor and inhibit HIV-1 infection

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prefLabel

Improved guanide compounds which bind the CXCR4 co-receptor and inhibit HIV-1 infection

@ast

Improved guanide compounds which bind the CXCR4 co-receptor and inhibit HIV-1 infection

@en

P1476

Improved guanide compounds which bind the CXCR4 co-receptor and inhibit HIV-1 infection

@en

P2093

Alan J Weaver

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Joyce B Shepard

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Kejing Song

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Martin Teintze

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Mohamed E Labib

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Royce A Wilkinson

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Seth H Pincus

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P2860

Involvement of chemokine receptors in breast cancer metastasis

Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists

AutoDock Vina: Improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading

Emergence of resistant human immunodeficiency virus type 1 in patients receiving fusion inhibitor (T-20) monotherapy.

Pharmacophore identification of a specific CXCR4 inhibitor, T140, leads to development of effective anti-HIV agents with very high selectivity indexes.

Conformational study of a highly specific CXCR4 inhibitor, T140, disclosing the close proximity of its intrinsic pharmacophores associated with strong anti-HIV activity.

Molecular-size reduction of a potent CXCR4-chemokine antagonist using orthogonal combination of conformation- and sequence-based libraries.

Structure-activity relationships of cyclic peptide-based chemokine receptor CXCR4 antagonists: disclosing the importance of side-chain and backbone functionalities.

Anti-CXCR4 monoclonal antibodies recognizing overlapping epitopes differ significantly in their ability to inhibit entry of human immunodeficiency virus type 1.

Antigenically distinct conformations of CXCR4.

P304

2197-2201

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P31

scholarly article

P356

10.1016/J.BMCL.2013.01.107

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P407

English

P433

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

P478

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

P577

2013-01-30T00:00:00Z

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P698

23434419

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P932

3624624

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