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3-Amino-7-phthalazinylbenzoisoxazoles as a Novel Class of Potent, Selective, and Orally Available Inhibitors of p38α Mitogen-Activated Protein Kinase.

Authors :
Liping H. Pettus
Shimin Xu
Guo-Qiang Cao
Partha P. Chakrabarti
Robert M. Rzasa
Kelvin Sham
Ryan P. Wurz
Dawei Zhang
Scott Middleton
Bradley Henkle
Matthew H. Plant
Christiaan J. M. Saris
Lisa Sherman
Lu Min Wong
David A. Powers
Yanyan Tudor
Violeta Yu
Matthew R. Lee
Rashid Syed
Faye Hsieh
Source :
Journal of Medicinal Chemistry. Oct2008, Vol. 51 Issue 20, p6280-6292. 13p.
Publication Year :
2008

Abstract

The p38 mitogen-activated protein kinase (MAPK) is a central signaling molecule in many proinflammatory pathways, regulating the cellular response to a multitude of external stimuli including heat, ultraviolet radiation, osmotic shock, and a variety of cytokines especially interleukin-1β and tumor necrosis factor α. Thus, inhibitors of this enzyme are postulated to have significant therapeutic potential for the treatment of rheumatoid arthritis, inflammatory bowel disease, osteoporosis, and many other diseases where aberrant cytokine signaling is the driver of disease. Herein, we describe a novel class of 3-amino-7-phthalazinylbenzoisoxazole-based inhibitors. With relatively low molecular weight, these compounds are highly potent in enzyme and cell-based assays, with minimal protein shift in 50% human whole blood. Compound 3cwas efficacious (ED 50= 0.05 mg/kg) in the rat collagen induced arthritis (CIA) model. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00222623
Volume :
51
Issue :
20
Database :
Academic Search Index
Journal :
Journal of Medicinal Chemistry
Publication Type :
Academic Journal
Accession number :
34832400
Full Text :
https://doi.org/10.1021/jm8005405