| Literature DB >> 29776742 |
Matthew W Martin1, Jennifer Y Lee2, David R Lancia2, Pui Yee Ng2, Bingsong Han2, Jennifer R Thomason2, Maureen S Lynes2, C Gary Marshall2, Chiara Conti2, Alan Collis2, Monica Alvarez Morales2, Kshama Doshi2, Aleksandra Rudnitskaya2, Lili Yao3, Xiaozhang Zheng2.
Abstract
N-Hydroxy-2-arylisoindoline-4-carboxamides are potent and selective inhibitors of HDAC11. The discovery, synthesis, and structure activity relationships of this novel series of inhibitors are reported. An advanced analog (FT895) displays promising cellular activity and pharmacokinetic properties that make it a useful tool to study the biology of HDAC11 and its potential use as a therapeutic target for oncology and inflammation indications.Entities:
Keywords: HDAC11; HDACs; Hydroxamic acid; Inflammation; Isoindoline; Oncology
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Year: 2018 PMID: 29776742 DOI: 10.1016/j.bmcl.2018.05.021
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823