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首页> 外文期刊>Chemical and Pharmaceutical Bulletin >Synthesis and structure activity relationship studies of benzothieno(3,2-b)furan derivatives as a novel class of IKKbeta inhibitors.
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Synthesis and structure activity relationship studies of benzothieno(3,2-b)furan derivatives as a novel class of IKKbeta inhibitors.

机译:苯并噻吩并(3,2-b)呋喃衍生物作为一类新的IKKbeta抑制剂的合成与结构活性关系研究。

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摘要

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.
机译:作为一类新型的IKKbeta抑制剂,根据已知的噻吩IKKbeta抑制剂的结构设计和合成了一系列三环呋喃衍生物。在各种合成的融合呋喃衍生物中,苯并噻吩并[3,2-b]呋喃衍生物13a在酶和细胞分析中显示出对IKKbeta的有效抑制活性。有效的抑制活性源自分子内非键合的S ... O相互作用,这已通过JNK3的16k X射线结构得到证实。在核心结构上引入其他取代基导致发现了6-烷氧基衍生物,该衍生物具有与13a相当的IKKbeta抑制活性,并具有改善的代谢稳定性。其中,发现适当的亲脂性化合物16a,h,i和13g(log D> 2)具有良好的口服生物利用度。

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