Browse views: by Year, by Function, by GLF, by Subfunction, by Conference, by Journal

Discovery of EGFR selective 4,6-disubstituted pyrimidines from a combinatorial kinase-directed heterocycle library.

Zhang, Qiong and Liu, Yi and Gao, Feng and Ding, Qiang and Cho, Charles and Hur, Wooyoung and Jin, Yunho and Uno, Tetsuo and Joazeiro, Claudio and Gray, Nathanael (2006) Discovery of EGFR selective 4,6-disubstituted pyrimidines from a combinatorial kinase-directed heterocycle library. Journal of the American Chemical Society, 128 (7). pp. 2182-2183. ISSN 0002-7863

Abstract

The epidermal growth factor receptor (EGFR) tyrosine kinase was one of the first receptor tyrosine kinases to be targeted for drug development by the pharmaceutical industry due to its ubiquitous overexpression in a variety of tumors. Despite the validation of several quinazoline-based scaffolds in the clinic, there is a dearth of alternative chemical structure classes that are capable of inhibiting EGFR kinase activity selectively. Here we describe the discovery of potent and highly selective 4,6-disubstituted pyrimidine inhibitors of enzymatic and cellular EGFR activity and provide an explanation for their exceptional degree of kinase selectivity.

Item Type: Article
Related URLs:
Additional Information: archiving not formally supported
Related URLs:
Date Deposited: 14 Dec 2009 14:04
Last Modified: 31 Jan 2013 01:26
URI: https://oak.novartis.com/id/eprint/160

Search

Email Alerts

Register with OAK to receive email alerts for saved searches.