Article ID Journal Published Year Pages File Type
1378026 Bioorganic & Medicinal Chemistry Letters 2007 5 Pages PDF
Abstract

We have modified the previously reported 2-aminoquinoline 1 to provide two novel series of MCH-1R antagonists. Representative compounds from the quinazoline and benzimidazole series have been shown to be potent and selective, with promising in vitro eADME profiles.

Graphical abstractThe discovery, synthesis, evaluation and structure–activity relationships of a series of quinazolines and benzimidazoles as MCH-1R antagonists are described.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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