| Literature DB >> 19361991 |
Jingrong Cao1, Huai Gao, Guy Bemis, Francesco Salituro, Mark Ledeboer, Edmund Harrington, Susanne Wilke, Paul Taslimi, S Pazhanisamy, Xiaoling Xie, Marc Jacobs, Jeremy Green.
Abstract
A series of N-benzylated isatin oximes were developed as inhibitors of the mitogen-activated kinase, JNK3. X-ray crystallographic structures aided in the design and synthesis of novel, selective compounds, that inhibit JNK3, but not p38 MAP kinase and provided key insights into understanding the behavior of gatekeeper residue methionine-146 in determining target selectivity for this series.Entities:
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Year: 2009 PMID: 19361991 DOI: 10.1016/j.bmcl.2009.03.043
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823