| Literature DB >> 12643946 |
Xuechun Zhang1, Godwin C G Pais, Evguenia S Svarovskaia, Christophe Marchand, Allison A Johnson, Rajeshri G Karki, Marc C Nicklaus, Vinay K Pathak, Yves Pommier, Terrence R Burke.
Abstract
Aryl beta-diketo acids (ADK) comprise a general class of potent HIV-1 integrase (IN) inhibitors, which can exhibit selective inhibition of strand transfer reactions in extracellular recombinant IN assays and provide potent antiviral effects in HIV-infected cells. Recent studies have shown that polycyclic aryl or aryl rings bearing aryl-containing substituents are components of potent members of this class. Reported herein is the first use of azido functionality as an aryl replacement in beta-diketo acid IN inhibitors. The ability of azido-containing inhibitors to exhibit potent inhibition of IN and antiviral protection in HIV-infected cells, renders the azide group of potential value in the further development of ADK-based IN inhibitors.Entities:
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Year: 2003 PMID: 12643946 DOI: 10.1016/s0960-894x(03)00059-3
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823