| Literature DB >> 31519373 |
Wei Meng1, Leonard P Adam2, Kamelia Behnia3, Lei Zhao2, Richard Yang2, Lisa M Kopcho3, Gregory A Locke3, David S Taylor2, Xiaohong Yin2, Ruth R Wexler4, Heather Finlay4.
Abstract
A series of benzothiazoles with a cyano group was synthesized and evaluated as endothelial lipase (EL) inhibitors for the potential treatment of cardiovascular diseases. Efforts to reduce molecular weight and polarity in the series led to improved physicochemical properties of these compounds, as well as selectivity for EL over hepatic lipase (HL). As a benchmark compound, 8i demonstrated potent EL activity, an acceptable absorption, distribution, metabolism and elimination (ADME) profile and pharmacokinetic (PK) exposure which allowed further evaluation in preclinical animal efficacy studies.Entities:
Keywords: Benzothiazole; Cardiovascular diseases; Endothelial lipase; High density lipoprotein; Structure-activity relationship
Year: 2019 PMID: 31519373 DOI: 10.1016/j.bmcl.2019.126673
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823