1251581-93-7Relevant articles and documents
Identification of benzofurano[3,2-d]pyrimidin-2-ones, a new series of HIV-1 nucleotide-competing reverse transcriptase inhibitors
Tremblay, Martin,Bethell, Richard C.,Cordingley, Michael G.,Deroy, Patrick,Duan, Jianmin,Duplessis, Martin,Edwards, Paul J.,Faucher, Anne-Marie,Halmos, Ted,James, Clint A.,Kuhn, Cyrille,Lacoste, Jean-éric,Lamorte, Louie,Laplante, Steven R.,Malenfant, éric,Minville, Joannie,Morency, Louis,Morin, Sébastien,Rajotte, Daniel,Salois, Patrick,Simoneau, Bruno,Tremblay, Sonia,Sturino, Claudio F.
, p. 2775 - 2780 (2013/06/27)
Screening of our sample collection led to the identification of a set of benzofurano[3,2-d]pyrimidine-2-one hits acting as nucleotide-competing HIV-1 reverse transcriptase inhibitiors (NcRTI). Significant improvement in antiviral potency was achieved when substituents were introduced at positions N1, C4, C7 and C8 on the benzofuranopyrimidone scaffold. The series was optimized from low micromolar enzymatic activity against HIV-1 RT and no antiviral activity to low nanomolar antiviral potency. Further profiling of inhibitor 30 showed promising overall in vitro properties and also demonstrated that its potency was maintained against viruses resistant to the other major classes of HIV-1 RT inhibitors.
INHIBITORS OF HIV REPLICATION
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, (2010/11/03)
Compounds of formula (I): wherein R1, R2, A1, A2, A3, A4, X and Y are as defined herein, are useful as inhibitors of HIV replication.
