Synthesis and anti-HIV activity of cosalane analogues incorporating two dichlorodisalicylmethane pharmacophore fragments. (Q43764160)

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12 November 2019

title

Synthesis and anti-HIV activity of cosalane analogues incorporating two dichlorodisalicylmethane pharmacophore fragments (English)

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12 November 2019

author

Christophe Pannecouque

3

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12 November 2019

author name string

A Casimiro-Garcia

1

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12 November 2019

E De Clercq

2

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12 November 2019

M Witvrouw

4

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12 November 2019

T L Loftus

5

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12 November 2019

J A Turpin

6

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12 November 2019

R W Buckheit

7

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12 November 2019

P E Fanwick

8

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12 November 2019

M Cushman

9

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12 November 2019

language of work or name

English

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publication date

1 November 2001

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Bioorganic & Medicinal Chemistry

12 November 2019

published in

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12 November 2019

volume

9

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12 November 2019

issue

11

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12 November 2019

page(s)

2827-2841

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Synthesis of a cosalane analog with an extended polyanionic pharmacophore conferring enhanced potency as an anti-HIV agent

12 November 2019

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Extension of the polyanionic cosalane pharmacophore as a strategy for increasing anti-HIV potency

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Synthesis and Anti-HIV Activity of Cosalane Analogues with Substituted Benzoic Acid Rings Attached to the Pharmacophore through Methylene and Amide Linkers

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Preparation and anti-HIV activities of aurintricarboxylic acid fractions and analogues: direct correlation of antiviral potency with molecular weight

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Design, synthesis, and biological evaluation of cosalane, a novel anti-HIV agent which inhibits multiple features of virus reproduction

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Aurintricarboxylic acid and Evans Blue represent two different classes of anionic compounds which selectively inhibit the cytopathogenicity of human T-cell lymphotropic virus type III/lymphadenopathy-associated virus

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Correlation of anti-HIV potency with lipophilicity in a series of cosalane analogs having normal alkenyl and phosphodiester chains as cholestane replacements

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New alkenyldiarylmethanes with enhanced potencies as anti-HIV agents which act as non-nucleoside reverse transcriptase inhibitors

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Synthesis and anti-HIV activity of cosalane analogues incorporating nitrogen in the linker chain

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Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride. Studies on Direct and Indirect Reductive Amination Procedures(1).

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Cosalane analogues with enhanced potencies as inhibitors of HIV-1 protease and integrase

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Exploration of the effects of linker chain modifications on anti-HIV activities in a series of cosalane analogues

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Mechanism of the Antiviral Activity of New Aurintricarboxylic Acid Analogues

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Thiazolobenzimidazole: biological and biochemical anti-retroviral activity of a new nonnucleoside reverse transcriptase inhibitor

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7 January 2021

Detection, Isolation, and Continuous Production of Cytopathic Retroviruses (HTLV-III) from Patients with AIDS and Pre-AIDS

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Isolation of a T-Lymphotropic Retrovirus from a Patient at Risk for Acquired Immune Deficiency Syndrome (AIDS)

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7 January 2021

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Identifiers

DOI

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12 November 2019

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