Structure, Stereochemistry, and Biological Activity of Integramycin, a Novel Hexacyclic Natural Product Produced by Actinoplanes sp. that Inhibits HIV-1 Integrase
Author:
Affiliation:
1. Merck Research Laboratories, Rahway, New Jersey 07065, and West Point, Pennsylvania 19486, and Centro de Investigación Básica, Laboratorios Merck Sharp & Dohme de Espana, S. A. Josefa Valcárcel 38, 28027 Madrid, Spain
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol025539b
Reference8 articles.
1. HIV Integrase, a Brief Overview from Chemistry to Therapeutics
2. Inhibitors of Strand Transfer That Prevent Integration and Inhibit HIV-1 Replication in Cells
3. 4-Aryl-2,4-dioxobutanoic Acid Inhibitors of HIV-1 Integrase and Viral Replication in Cells
4. Structure-based HIV-1 integrase inhibitor design: a future perspective
5. Equisetin and a novel opposite stereochemical homolog phomasetin, two fungal metabolites as inhibitors of HIV-1 integrase
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