Literature DB >> 20346653

Amide-based inhibitors of p38alpha MAP kinase. Part 1: discovery of novel N-pyridyl amide lead molecules.

Gregory R Luedtke1, Kurt Schinzel, Xuefei Tan, Richland W Tester, Imad Nashashibi, Yong-Jin Xu, Sundeep Dugar, Daniel E Levy, Joon Jung.   

Abstract

A novel series of N-pyridyl amides as potent p38alpha kinase inhibitors is described. Based on the structural similarities between the initial hit and a well-known imidazole pyrimidine series of p38alpha inhibitors, potencies within the newly discovered series were quickly improved by installation of an (S)-alpha-methylbenzyl moiety at the 2-position of the pyridine ring. The proposed binding modes of the new series to p38alpha were evaluated against SAR findings and provided rationale for further development of this series of molecules. Copyright 2010 Elsevier Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20346653     DOI: 10.1016/j.bmcl.2010.02.088

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


  1 in total

1.  Efficient electrochemical N-alkylation of N-boc-protected 4-aminopyridines: towards new biologically active compounds.

Authors:  Marta Feroci; Isabella Chiarotto; Gianpiero Forte; Giovanna Simonetti; Felicia Diodata D'Auria; Louis Maes; Daniela De Vita; Luigi Scipione; Laura Friggeri; Roberto Di Santo; Silvano Tortorella
Journal:  ISRN Org Chem       Date:  2014-03-05
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.