| Literature DB >> 28454672 |
Jun Tang1, Stacey A Jones2, Jerry L Jeffrey2, Sonia R Miranda2, Cristin M Galardi2, David M Irlbeck2, Kevin W Brown2, Charlene B McDanal2, Brian A Johns2.
Abstract
A new class of betulin-derived α-keto amides was identified as HIV-1 maturation inhibitors. Through lead optimization, GSK8999 was identified with IC50 values of 17nM, 23nM, 25nM, and 8nM for wild type, Q369H, V370A, and T371A respectively. When tested in a panel of 62 HIV-1 isolates covering a diversity of CA-SP1 genotypes including A, AE, B, C, and G using a PBMC based assay, GSK8999 was potent against 57 of 62 isolates demonstrating an improvement over the first generation maturation inhibitor BVM. The data disclosed here also demonstrated that the new α-keto amide GSK8999 has a mechanism of action consistent with inhibition of the proteolytic cleavage of CA-SP1.Entities:
Keywords: Betulin; Bevirimat; GSK8999; HIV-1; Maturation inhibitor
Mesh:
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Year: 2017 PMID: 28454672 DOI: 10.1016/j.bmcl.2017.04.042
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823