| Literature DB >> 16337120 |
Britt-Marie Swahn1, Yafeng Xue, Erwan Arzel, Elisabet Kallin, Angelika Magnus, Niklas Plobeck, Jenny Viklund.
Abstract
The design and synthesis of a new series of c-Jun N-terminal kinase-3 (JNK3) inhibitors with selectivity against JNK1 are reported. The novel series of substituted 2'-anilino-4,4'-bipyridines were designed based on a combination of hits from high throughput screening and X-ray crystal structure information of compounds crystallized into the JNK3 ATP binding active site.Entities:
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Year: 2005 PMID: 16337120 DOI: 10.1016/j.bmcl.2005.11.039
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823