About

Log in?

DTU users get better search results including licensed content and discounts on order fees.

Anyone can log in and get personalized features such as favorites, tags and feeds.

Log in as DTU user Log in as non-DTU user No thanks

DTU Findit

Book chapter

Kinase Inhibitors

In Drug Selectivity: an Evolving Concept in Medicinal Chemistry — 2018, pp. 31-53
From

Department of Chemistry, Technical University of Denmark1

University of Copenhagen2

The strategy of applying kinase inhibitors as effective therapeutic agents has achieved unparalleled success in the past decade, while it is still a daunting challenge to develop kinase inhibitors with desirable selectivity among different kinase families. This chapter describes the basic conceptions in the field of kinase selectivity, available profiling technologies, and quantification of selectivity levels.

The chapter highlights the different selectivity of approved kinase inhibitors, which include non‐covalent type I and II ATP‐competitive inhibitors, allosteric inhibitors, one lipid kinase inhibitor, and covalent inhibitors. Most approved kinase inhibitors are multitarget or unselective inhibitors that bind with the highly conserved ATP pocket, high selectivity is more likely to be achieved among kinases with only few closely related homologs or unique structural features in binding sites.

Language: English
Publisher: Wiley
Year: 2018
Pages: 31-53
Journal subtitle: An Evolving Concept in Medicinal Chemistry
ISBN: 3527335382 , 3527674381 , 3527674403 , 3527674411 , 9783527335381 , 9783527674381 , 9783527674404 and 9783527674411
Types: Book chapter
DOI: 10.1002/9783527674381.ch2
ORCIDs: Wu, Peng and 0000-0001-5004-8609

DTU users get better search results including licensed content and discounts on order fees.

Log in as DTU user

Access

Analysis