| Literature DB >> 10576692 |
M Patel1, R J McHugh, B C Cordova, R M Klabe, S Erickson-Viitanen, G L Trainor, S S Ko.
Abstract
Two series of benzoxazinones differing in the aromatic substitution pattern were prepared and evaluated as HIV-1 reverse transcriptase inhibitors. The 5-fluoro (5a-d) and 6-nitro (5e-h) substituted compounds displayed activity comparable or better than Efavirenz, the lead structure of the series.Entities:
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Year: 1999 PMID: 10576692 DOI: 10.1016/s0960-894x(99)00565-x
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823