| Literature DB >> 24981264 |
Abstract
Traditionally, protein kinases have been regarded as non-druggable targets, instead they play a central role in physiological and pathophysiological processes. This changed when STI571, an inhibitor of the Bcr-Abl kinase, known as Gleevec, reached the market as the first designer drug. Ever since, kinase-directed research and development (R&D) expanded rapidly, leading to more than 45 clinically relevant kinase inhibitors. At a comparable pace the kinase-based technologies matured, cumulating in the development of sophisticated chemogenetic and chemoproteomic tools, which are referred to as chemical kinomics.:Entities:
Year: 2004 PMID: 24981264 DOI: 10.1016/j.ddtec.2004.08.013
Source DB: PubMed Journal: Drug Discov Today Technol ISSN: 1740-6749