Literature DB >> 21185722

Azaindoles as potent CRTH2 receptor antagonists.

Daniel Simard1, Yves Leblanc, Carl Berthelette, M Helmi Zaghdane, Carmela Molinaro, Zhaoyin Wang, Michel Gallant, Stephen Lau, Trinh Thao, Martine Hamel, Rino Stocco, Nicole Sawyer, Susan Sillaots, Francois Gervais, Robert Houle, Jean-François Lévesque.   

Abstract

A new class of 7-azaindole analogs of MK-7246 as potent and selective CRTH2 antagonists is reported. The SAR leading to the identification of the optimal azaindole regioisomer as well as the pharmacokinetics and off-target activities of the most potent antagonists are disclosed. Copyright Â
© 2010 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 21185722     DOI: 10.1016/j.bmcl.2010.11.084

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


  2 in total

1.  Access to pyrrolo-pyridines by gold-catalyzed hydroarylation of pyrroles tethered to terminal alkynes.

Authors:  Elena Borsini; Gianluigi Broggini; Andrea Fasana; Chiara Baldassarri; Angelo M Manzo; Alcide D Perboni
Journal:  Beilstein J Org Chem       Date:  2011-10-26       Impact factor: 2.883

2.  Xanthate based radical cascade toward multicomponent formation of pyrrolopyrimidines.

Authors:  Laurent El Kaïm; Laurence Grimaud; Patil Pravin
Journal:  Molecules       Date:  2011       Impact factor: 4.411

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.