| Literature DB >> 25589915 |
Simon J Mountford1, Zhaohua Zheng2, Krithika Sundaram1, Ian G Jennings1, Justin R Hamilton3, Philip E Thompson1.
Abstract
The Class II PI3 kinases are emerging from the shadows of their Class I cousins. The data emerging from PIK3C2 genetic modification studies and from siRNA knockdown suggest important roles in physiology and pathology. With some well-studied Class I isoform inhibitors showing strong Class II activity and a wealth of crystallographic information available, the structural similarity of these isoforms to Class I provides both the opportunity and the challenge in design of selective pharmacological inhibitors.Keywords: Class II; PI3 kinase; isoform selectivity
Year: 2014 PMID: 25589915 PMCID: PMC4291705 DOI: 10.1021/ml500354e
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345