Literature DB >> 14643346

trans-3,4-dimethyl-4-(3-carboxamidophenyl)piperidines: a novel class of micro-selective opioid antagonists.

Bertrand Le Bourdonnec1, Serge Belanger, Joel A Cassel, Gabriel J Stabley, Robert N DeHaven, Roland E Dolle.   

Abstract

trans-3,4-Dimethyl-4-(3-carboxamidophenyl)piperidines constitute a novel class of micro opioid receptor antagonists. The CONH(2) group was found to be an effective isostere of the phenolic OH moiety. Structure-activity relationships at the piperidine nitrogen position led to the identification of several ligands displaying high affinity toward the cloned human micro opioid receptors, good selectivity micro/delta, micro/kappa, and potent in vitro antagonist activity.

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Year:  2003        PMID: 14643346     DOI: 10.1016/j.bmcl.2003.09.012

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


  3 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

2.  Agonist vs antagonist behavior of delta opioid peptides containing novel phenylalanine analogues in place of Tyr(1).

Authors:  Irena Berezowska; Nga N Chung; Carole Lemieux; Brian C Wilkes; Peter W Schiller
Journal:  J Med Chem       Date:  2009-11-12       Impact factor: 7.446

3.  μ Opioid receptor: novel antagonists and structural modeling.

Authors:  Teresa Kaserer; Aquilino Lantero; Helmut Schmidhammer; Mariana Spetea; Daniela Schuster
Journal:  Sci Rep       Date:  2016-02-18       Impact factor: 4.379

  3 in total

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