| Literature DB >> 17409557 |
Hideyuki Sugiyama1, Masato Yoshida, Kouji Mori, Tomohiro Kawamoto, Satoshi Sogabe, Terufumi Takagi, Hideyuki Oki, Toshimasa Tanaka, Hiroyuki Kimura, Yoshinori Ikeura.
Abstract
As a novel class of IKKbeta inhibitors, a series of tricyclic furan derivatives was designed and synthesized based on the structure of known thiophene IKKbeta inhibitors. Among the various fused furan derivatives synthesized, a benzothieno[3,2-b]furan derivative 13a displayed potent inhibitory activity towards IKKbeta in enzymatic and cellular assays. The potent inhibitory activity originates from an intramolecular non-bonded S...O interaction which was confirmed by the X-ray structure of JNK3 with 16k. The introduction of further substituents on the core structure led to the discovery of the 6-alkoxy derivatives, which possessed a comparable IKKbeta inhibitory activity to 13a and an improved metabolic stability. Among these, appropriately lipophilic compounds 16a, h, i, and 13g (log D>2) were found to possess good oral bioavailability.Entities:
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Year: 2007 PMID: 17409557 DOI: 10.1248/cpb.55.613
Source DB: PubMed Journal: Chem Pharm Bull (Tokyo) ISSN: 0009-2363 Impact factor: 1.645