Discovery of novel HIV entry inhibitors for the CXCR4 receptor by prospective virtual screening. (Q33428717)

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25 January 2020

title

Discovery of novel HIV entry inhibitors for the CXCR4 receptor by prospective virtual screening (English)

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25 January 2020

author

Violeta I Pérez-Nueno

1

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25 January 2020

David W. Ritchie

3

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25 January 2020

José I Borrell

4

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25 January 2020

Jordi Teixidó

5

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25 January 2020

author name string

Sofia Pettersson

2

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25 January 2020

publication date

1 April 2009

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Journal of Chemical Information and Modeling

25 January 2020

language of work or name

English

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published in

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25 January 2020

volume

49

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25 January 2020

issue

4

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25 January 2020

page(s)

810-823

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How does consensus scoring work for virtual library screening? An idealized computer experiment

25 January 2020

cites work

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Comparison of ligand-based and receptor-based virtual screening of HIV entry inhibitors for the CXCR4 and CCR5 receptors using 3D ligand shape matching and ligand-receptor docking

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Activity of different bicyclam derivatives against human immunodeficiency virus depends on their interaction with the CXCR4 chemokine receptor

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Mutation of Asp(171) and Asp(262) of the chemokine receptor CXCR4 impairs its coreceptor function for human immunodeficiency virus-1 entry and abrogates the antagonistic activity of AMD3100.

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AMD3465, a monomacrocyclic CXCR4 antagonist and potent HIV entry inhibitor

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A duodenally absorbable CXC chemokine receptor 4 antagonist, KRH-1636, exhibits a potent and selective anti-HIV-1 activity

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Molecular mechanism of action of monocyclam versus bicyclam non-peptide antagonists in the CXCR4 chemokine receptor

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Identifiers

DOI

10.1021/CI800468Q

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19358515%20AND%20SRC:MED&resulttype=core&format=json

journals/jcisd/Perez-NuenoPRBT09

25 January 2020

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference