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Discovery of 3-(1H-Indol-3-yl)-4-[2-(4-methylpiperazin-1-yl)quinazolin-4-yl]pyrrole-2,5-dione (AEB071), a Potent and Selective Inhibitor of Protein Kinase C Isotypes
Journal of Medicinal Chemistry ( IF 6.8 ) Pub Date : 2009-09-18 00:00:00 , DOI: 10.1021/jm901108b
Jürgen Wagner 1 , Peter von Matt 1 , Richard Sedrani 1 , Rainer Albert 1 , Nigel Cooke 1 , Claus Ehrhardt 1 , Martin Geiser 1 , Gabriele Rummel 1 , Wilhelm Stark 1 , Andre Strauss 1 , Sandra W. Cowan-Jacob 1 , Christian Beerli 1 , Gisbert Weckbecker 1 , Jean-Pierre Evenou 1 , Gerhard Zenke 1 , Sylvain Cottens 1
Affiliation  

A series of novel maleimide-based inhibitors of protein kinase C (PKC) were designed, synthesized, and evaluated. AEB071 (1) was found to be a potent, selective inhibitor of classical and novel PKC isotypes. 1 is a highly efficient immunomodulator, acting via inhibition of early T cell activation. The binding mode of maleimides to PKCs, proposed by molecular modeling, was confirmed by X-ray analysis of 1 bound in the active site of PKCα.

中文翻译:

3-(1 H-吲哚-3-基)-4- [2-(4-甲基哌嗪-1-基)喹唑啉-4-基]吡咯-2,5-二酮(AEB071)的发现蛋白激酶C同种型抑制剂

设计,合成和评估了一系列新型的基于马来酰亚胺的蛋白激酶C(PKC)抑制剂。发现AEB071(1)是经典和新型PKC同种型的有效选择性抑制剂。图1是高效的免疫调节剂,其通过抑制早期T细胞活化而起作用。通过分子建模提出的马来酰亚胺与PKCs的结合模式,通过对PKCα活性位点中结合的1个X射线分析进行了证实。
更新日期:2009-09-18
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