4.5 Article

Ureas with histamine H3-antagonist receptor activity -: A new scaffold discovered by lead-hopping from cinnamic acid amides

Journal

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume 16, Issue 20, Pages 5303-5308

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2006.07.093

Keywords

histamine H-3 receptor; hH(3)-receptor; urea; hERG

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A group of tri and tetrasubstituted urea derivatives have been found to be hH(3)-antagonists. The most potent compounds were found in the class of (piperazine-1-yl)-(piperidine-1-yl)-methanones which in addition showed negligible hERG inhibition. (c) 2006 Elsevier Ltd. All rights reserved.

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