| Literature DB >> 27994759 |
Francisco Velázquez1, Mariappan Chelliah1, Martin Clasby1, Zhuyan Guo1, John Howe1, Randy Miller1, Santhosh Neelamkavil1, Unmesh Shah1, Aileen Soriano1, Yan Xia1, Srikanth Venkatraman1, Samuel Chackalamannil1, Ian W Davies1.
Abstract
A new class of hepatitis C NS3/4A inhibitors was identified by introducing a novel spirocyclic proline-P2 surrogate onto the P2-P4 macrocyclic core of MK-5172 (grazoprevir). The potency profile of new analogues showed excellent pan-genotypic activity for most compounds. The potency evaluation included the most difficult genotype 3a (EC50 values ≤10 nM) and other key genotype 1b mutants. Molecular modeling was used to design new target compounds and rationalize our results. A synthetic approach based on the Julia-Kocienski olefination and macrolactamization to assemble the P2-P4 macrocyclic core containing the novel spirocyclic proline-P2 moiety is presented as well.Entities:
Keywords: HCV; HCV NS3/4A; Hepatitis C; MK-5172; MK-8831; antivirals
Year: 2016 PMID: 27994759 PMCID: PMC5150670 DOI: 10.1021/acsmedchemlett.6b00321
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345