Structure−Activity Relationships: Analogues of the Dicaffeoylquinic and Dicaffeoyltartaric Acids as Potent Inhibitors of Human Immunodeficiency Virus Type 1 Integrase and Replication
Author:
Affiliation:
1. Departments of Microbiology and Molecular Genetics and of Pathology, University of California, Irvine, California 92697-4800, and Department of Chemistry, Texas Christian University, Fort Worth, Texas
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm9804735
Reference47 articles.
1. Requirement of active human immunodeficiency virus type 1 integrase enzyme for productive infection of human T-lymphoid cells
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