Literature DB >> 26927018

Identification of an active metabolite of PAR-1 antagonist RWJ-58259 and synthesis of analogues to enhance its metabolic stability.

Eifion Robinson1, Emily Knight1, Natalia Smoktunowicz2, Rachel C Chambers2, Graham G Inglis3, Vijay Chudasama1, Stephen Caddick1.   

Abstract

The discontinuation of PAR-1 antagonist RWJ-58259 beyond use as a biological probe is most likely due to it's short half-life in vivo. However, retention of significant in vivo activity beyond the point where most of the RWJ-58259 had been consumed implies the generation of an active metabolite. Herein we describe the biological activity of a predicted metabolite of RWJ-58259 and the synthesis of analogues designed to enhance the metabolic stability of RWJ-58259.

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Year:  2016        PMID: 26927018     DOI: 10.1039/c6ob00332j

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  2 in total

1.  Characterization of Protease-Activated Receptor (PAR) ligands: Parmodulins are reversible allosteric inhibitors of PAR1-driven calcium mobilization in endothelial cells.

Authors:  Disha M Gandhi; Mark W Majewski; Ricardo Rosas; Kaitlin Kentala; Trevor J Foster; Eric Greve; Chris Dockendorff
Journal:  Bioorg Med Chem       Date:  2018-04-06       Impact factor: 3.641

2.  An optimized procedure for direct access to 1H-indazole-3-carboxaldehyde derivatives by nitrosation of indoles.

Authors:  Arnaud Chevalier; Abdelaaziz Ouahrouch; Alexandre Arnaud; Thibault Gallavardin; Xavier Franck
Journal:  RSC Adv       Date:  2018-04-09       Impact factor: 3.361

  2 in total

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