Discovery of an Aurora kinase inhibitor through site-specific dynamic combinatorial chemistry
作者:Mark T. Cancilla、Molly M. He、Nina Viswanathan、Robert L. Simmons、Meggin Taylor、Amy D. Fung、Kathy Cao、Daniel A. Erlanson
DOI:10.1016/j.bmcl.2008.06.011
日期:2008.7
lead discovery method that combines site-directed ligand discovery with dynamic combinatorial chemistry. Our technique targets dynamic combinatorial screening to a specified region of a protein by using reversible disulfide chemistry. We have used this technology to rapidly identify inhibitors of the drug target Aurora A that span the purine-binding site and the adaptive pocket of the kinase. The binding
The present invention provides compounds and libraries of compounds having formula (I):
wherein L, n, S and A are defined generally and subsets herein. These compounds and libraries of compounds are useful generally in the drug discovery process.
[EN] IDENTIFICATION OF KINASE INHIBITORS<br/>[FR] IDENTIFICATION D'INHIBITEURS DE KINASE