299434-73-4Relevant articles and documents
Synthesis and evaluation of quinoxalinones as HIV-1 reverse transcriptase inhibitors
Patel, Mona,McHugh Jr., Robert J.,Cordova, Beverly C.,Klabe, Ronald M.,Erickson-Viitanen, Susan,Trainor, George L.,Rodgers, James D.
, p. 1729 - 1731 (2007/10/03)
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. (C) 2000 Dupont Pharmaceuticals Company. Published by Elsevier Science Ltd. All rights reserved.