| Literature DB >> 14643315 |
Abdellah Benjahad1, Jérôme Guillemont, Koen Andries, Chi Hung Nguyen, David S Grierson.
Abstract
Building upon the potent anti-HIV-1 activities observed for the 3-dimethylamino-4-benzylpyridinone 2, and the corresponding 4-aryloxypyridinone analogue 3, a concise and efficient route to the 3-iodo-4-aryloxypyridinones 14a-c (IOPY's) was developed. This involved reaction of the 4-hydroxy substituted pyridinone 10 with the requisite dichloroiodobenzene reagent 11. IOPY compound 14c is active at IC(50)=1-45 nM against wild type HIV-1 and a panel of six major simple/double HIV mutant strains.Entities:
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Year: 2003 PMID: 14643315 DOI: 10.1016/j.bmcl.2003.09.045
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823