Literature DB >> 17980586

Structure activity relationship studies of carboxamido-biaryl ethers as opioid receptor antagonists (OpRAs). Part 2.

Kumiko Takeuchi1, William G Holloway, Charles H Mitch, Steven J Quimby, Jamie H McKinzie, Todd M Suter, Michael A Statnick, Peggy L Surface, Paul J Emmerson, Elizabeth M Thomas, Miles G Siegel.   

Abstract

A series of 6-bicycloaryloxynicotinamides were identified as opioid receptor antagonists at mu, kappa, and delta receptors. Compounds in the 6-(2,3,4,5-tetrahydro-1H-benzo[c]azepin-7-yloxy)nicotinamide scaffold exhibited potent in vitro functional antagonism at all three receptors.

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Year:  2007        PMID: 17980586     DOI: 10.1016/j.bmcl.2007.10.025

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

Review 1.  The discovery and development of the N-substituted trans-3,4-dimethyl-4-(3'-hydroxyphenyl)piperidine class of pure opioid receptor antagonists.

Authors:  F Ivy Carroll; Roland E Dolle
Journal:  ChemMedChem       Date:  2014-06-30       Impact factor: 3.466

  1 in total

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