| Literature DB >> 10937734 |
M Patel1, R J McHugh, B C Cordova, R M Klabe, S Erickson-Viitanen, G L Trainor, J D Rodgers.
Abstract
A series of 3,3-disubstituted quinoxalinones was prepared and evaluated as HIV-1 reverse transcriptase inhibitors. The N-allyl (6b and 6f), N-cyclopropylmethyl (6a, 6g, 6h, and 6k) and N-carboalkoxy (6m-6y) substituted compounds displayed activity comparable or better than Efavirenz and GW420867X.Entities:
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Year: 2000 PMID: 10937734 DOI: 10.1016/s0960-894x(00)00321-8
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823