(Q32039175)

5 July 2017

title

Combinatorial synthesis of CCR5 antagonists (English)

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5 July 2017

Willoughby CA

1

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5 July 2017

Berk SC

2

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5 July 2017

Rosauer KG

3

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5 July 2017

Degrado S

4

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5 July 2017

Chapman KT

5

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5 July 2017

Gould SL

6

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5 July 2017

Springer MS

7

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Malkowitz L

8

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5 July 2017

Schleif WA

9

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Hazuda D

10

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Miller M

11

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5 July 2017

Kessler J

12

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5 July 2017

Danzeisen R

13

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Holmes K

14

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Lineberger J

15

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5 July 2017

Carella A

16

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5 July 2017

Carver G

17

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5 July 2017

Emini EA

18

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5 July 2017

language of work or name

English

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publication date

1 December 2001

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Bioorganic & Medicinal Chemistry Letters

5 July 2017

published in

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5 July 2017

volume

11

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5 July 2017

issue

24

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5 July 2017

page(s)

3137-3141

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Rapid identification of subtype-selective agonists of the somatostatin receptor through combinatorial chemistry

5 July 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900652-7

7 January 2021

Combinatorial diversification of indinavir: in vivo mixture dosing of an HIV protease inhibitor library

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A combinatorial approach defines specificities of members of the caspase family and granzyme B. Functional relationships established for key mediators of apoptosis

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7 January 2021

Human chemokines: an update

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Host factors and the pathogenesis of HIV-induced disease

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Homozygous defect in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection

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7 January 2021

The role of viral phenotype and CCR-5 gene defects in HIV-1 transmission and disease progression

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7 January 2021

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. part 1: discovery and initial structure-activity relationships for 1 -amino-2-phenyl-4-(piperidin-1-yl)butanes

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https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900652-7

7 January 2021

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 2: structure-activity relationships for substituted 2-Aryl-1-[N-(methyl)-N-(phenylsulfonyl)amino]-4-(piperidin-1-yl)butanes

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https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900652-7

7 January 2021

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 1: discovery of the pyrrolidine scaffold and determination of its stereochemical requirements

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https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900652-7

7 January 2021

1,3,4-Trisubstituted pyrrolidine CCR5 receptor antagonists. Part 2: lead optimization affording selective, orally bioavailable compounds with potent anti-HIV activity

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https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900652-7

7 January 2021

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 3: a proposed pharmacophore model for 1-[N-(methyl)-N-(phenylsulfonyl)amino]-2-(phenyl)-4-[4-(substituted)piperidin-1-yl]butanes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900652-7

7 January 2021

Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 4: synthesis and structure-activity relationships for 1-[N-(methyl)-N-(phenylsulfonyl)amino]-2-(phenyl)-4-(4-(N-(alkyl)-N-(benzyloxycarbonyl)amino)piperidin-1-yl)butanes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900652-7

7 January 2021

Mass spectrometry screening of combinatorial mixtures, correlation of measured and predicted electrospray ionization spectra

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https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900652-7

7 January 2021

Epitope mapping of CCR5 reveals multiple conformational states and distinct but overlapping structures involved in chemokine and coreceptor function

1 reference

https://api.crossref.org/works/10.1016%2FS0960-894X%2801%2900652-7

7 January 2021

10.1016/S0960-894X(01)00652-7

Identifiers

DOI

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5 July 2017

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