| Literature DB >> 34023664 |
Yun Ding1, Svetlana Belyanskaya2, Jennifer L DeLorey2, Jeffrey A Messer2, G Joseph Franklin2, Paolo A Centrella2, Barry A Morgan2, Matthew A Clark2, Steven R Skinner2, Jason W Dodson3, Peng Li3, Joseph P Marino3, David I Israel2.
Abstract
Inhibition of soluble epoxide hydrolase (sEH) has recently emerged as a new approach to treat cardiovascular disease and respiratory disease. Inhibitors based on 1,3,5-triazine chemotype were discovered through affinity selection against two triazine-based DNA-encoded libraries. The structure and activity relationship study led to the expansion of the original 1,4-cycloalkyl series to related aniline, piperidine, quinoline, aryl-ether and benzylic series. The 1,3-cycloalkyl chemotype led to the discovery of a clinical candidate (GSK2256294) for COPD.Entities:
Keywords: DNA-encoded library technology; Soluble epoxide hydrolase
Year: 2021 PMID: 34023664 DOI: 10.1016/j.bmc.2021.116216
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641