| Literature DB >> 22118668 |
Abstract
Tyrosine kinase inhibitors such as imatinib, dasatinib, and nilotinib interfere with ATP-binding pocket to inhibit BCR-ABL1 kinase. A recent report in Cell by Grebien et al. paves the way for a new approach to target BCR-ABL1 kinase by interfering with its SH2-kinase domain interface.Entities:
Year: 2011 PMID: 22118668 PMCID: PMC3228864 DOI: 10.1016/j.chembiol.2011.11.001
Source DB: PubMed Journal: Chem Biol ISSN: 1074-5521