Anti-HIV-1 Activity of Chemically Modified Heparins: Correlation between Binding to the V3 Loop of gp120 and Inhibition of Cellular HIV-1 Infection in vitro-Reference-Cited by-同舟云学术

Anti-HIV-1 Activity of Chemically Modified Heparins: Correlation between Binding to the V3 Loop of gp120 and Inhibition of Cellular HIV-1 Infection in vitro

Published:1994-06-07 Issue:22 Volume:33 Page:6974-6980
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Rider Christopher C.,Coombe Deirdre R.,Harrop Hilary A.,Hounsell Elizabeth F.,Bauer Christopher,Feeney James,Mulloy Barbara,Mahmood Naheed,Hay Alan,Parish Christopher R.

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi00188a029

Reference44 articles.

1. Pentosan polysulfate, a sulfated oligosaccharide, is a potent and selective anti-HIV agent in vitro

2. Mechanism of inhibitory effect of dextran sulfate and heparin on replication of human immunodeficiency virus in vitro.

3. 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

4. The V3 region of the envelope glycoprotein of human immunodeficiency virus type 1 binds sulfated polysaccharides and CD4-derived synthetic peptides.

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