Literature DB >> 16945534

p38 MAP kinase inhibitors. Part 5: discovery of an orally bio-available and highly efficacious compound based on the 7-amino-naphthyridone scaffold.

Swaminathan R Natarajan1, Luping Liu, Mark Levorse, James E Thompson, Edward A O'Neill, Stephen J O'Keefe, Kalpit A Vora, Raymond Cvetovich, John Y Chung, Ester Carballo-Jane, Denise M Visco.   

Abstract

A new sub-class of p38 inhibitors represented by 7-amino-naphthyridone have been discovered. Benchmark compound 16 potently inhibited p38 in vitro, was functionally active, and displayed excellent pharmacokinetic profiles in two animal species. Compound 16 reduced inflammation in animal disease models at EC(50) doses as low as 0.2mpk.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16945534     DOI: 10.1016/j.bmcl.2006.06.084

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


  1 in total

1.  2-Hydr-oxy-16-[(E)-4-hydr-oxy-3-methoxy-benzyl-idene]-13-(4-hydr-oxy-3-methoxy-phen-yl)-11-methyl-1,11-diaza-penta-cyclo-[12.3.1.0.0.0]octa-deca-3(8),4,6-triene-9,15-dione.

Authors:  Raju Suresh Kumar; Hasnah Osman; Mohamed Ashraf Ali; Madhukar Hemamalini; Hoong-Kun Fun
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2010-05-15
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.