Literature DB >> 16879964

A novel class of AMPA receptor allosteric modulators. Part 1: design, synthesis, and SAR of 3-aryl-4-cyano-5-substituted-heteroaryl-2-carboxylic acid derivatives.

Maria-Carmen Fernandez1, Ana Castaño, Esteban Dominguez, Ana Escribano, Delu Jiang, Alma Jimenez, Eric Hong, William J Hornback, Eric S Nisenbaum, Nancy Rankl, Eric Tromiczak, Grant Vaught, Hamideh Zarrinmayeh, Dennis M Zimmerman.   

Abstract

The synthesis and initial SAR studies of novel, highly potent positive allosteric modulators of AMPA receptors based on 3-(4-tert-butylphenyl)-4-cyano-5-methylsulfanyl-thiophene-2-carboxylic acid (6a) are described. SAR studies at the thioether moiety indicated that substitution at this position was mandatory and better potency was achieved with small groups.

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Year:  2006        PMID: 16879964     DOI: 10.1016/j.bmcl.2006.07.035

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


  3 in total

1.  Functional analysis of a novel positive allosteric modulator of AMPA receptors derived from a structure-based drug design strategy.

Authors:  Jonathan E Harms; Morris Benveniste; John K F Maclean; Kathryn M Partin; Craig Jamieson
Journal:  Neuropharmacology       Date:  2012-06-23       Impact factor: 5.250

2.  Functional insight into development of positive allosteric modulators of AMPA receptors.

Authors:  Autumn M Weeks; Jonathan E Harms; Kathryn M Partin; Morris Benveniste
Journal:  Neuropharmacology       Date:  2014-05-27       Impact factor: 5.250

3.  A high-throughput screen against pantothenate synthetase (PanC) identifies 3-biphenyl-4-cyanopyrrole-2-carboxylic acids as a new class of inhibitor with activity against Mycobacterium tuberculosis.

Authors:  Anuradha Kumar; Allen Casey; Joshua Odingo; Edward A Kesicki; Garth Abrahams; Michal Vieth; Thierry Masquelin; Valerie Mizrahi; Philip A Hipskind; David R Sherman; Tanya Parish
Journal:  PLoS One       Date:  2013-11-07       Impact factor: 3.240

  3 in total

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