Issue 5, 2011

Synthesis and SAR studies of benzimidazole derivatives as melanin concentrating hormonereceptor 1 (MCHR1) antagonists: Focus to detune hERG inhibition

Abstract

Melanin concentrating hormone receptor 1 (MCHR1) antagonists are potentially useful in the treatment of several CNS disorders such as obesity, stress, depression and anxiety. In a previous article, we have described a novel series of benzimidazoles as MCHR1 antagonists. These compounds showed good efficacy in obesity models but the lead compound also showed potent inhibition of hERG potassium channel. Described herein the medicinal chemistry attempts to reduce hERG inhibition while retaining MCHR1 antagonistic profile.

Graphical abstract: Synthesis and SAR studies of benzimidazole derivatives as melanin concentrating hormone receptor 1 (MCHR1) antagonists: Focus to detune hERG inhibition

Article information

Article type
Concise Article
Submitted
18 Jan 2011
Accepted
06 Feb 2011
First published
07 Mar 2011

Med. Chem. Commun., 2011,2, 385-389

Synthesis and SAR studies of benzimidazole derivatives as melanin concentrating hormone receptor 1 (MCHR1) antagonists: Focus to detune hERG inhibition

P. K. Sasmal, S. Sasmal, C. Abbineni, B. Venkatesham, P. T. Rao, M. Roshaiah, I. Khanna, V. J. Sebastian, J. Suresh, M. P. Singh, R. Talwar, D. Shashikumar, K. H. Reddy, T. M. Frimurer, Ø. Rist, L. Elster and T. Högberg, Med. Chem. Commun., 2011, 2, 385 DOI: 10.1039/C1MD00015B

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