Literature DB >> 31519373

Benzothiazole-based compounds as potent endothelial lipase inhibitors.

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.
Copyright © 2019. Published by Elsevier Ltd.

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


  1 in total

Review 1.  Current advances in the synthetic strategies of 2-arylbenzothiazole.

Authors:  Ayushi Sethiya; Nusrat Sahiba; Pankaj Teli; Jay Soni; Shikha Agarwal
Journal:  Mol Divers       Date:  2020-11-12       Impact factor: 2.943

  1 in total

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