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2-丙醇的3,6-二溴咔唑哌嗪衍生物作为通过Bax通道调节细胞色素c释放的首批抑制剂。

3,6-dibromocarbazole piperazine derivatives of 2-propanol as first inhibitors of cytochrome c release via Bax channel modulation.

作者信息

Bombrun Agnes, Gerber Patrick, Casi Giulio, Terradillos Olivier, Antonsson Bruno, Halazy Serge

机构信息

Serono Pharmaceutical Research Institute, 14 Chemin des Aulx, 1228 Plan-les-Ouates, Geneva, Switzerland.

出版信息

J Med Chem. 2003 Oct 9;46(21):4365-8. doi: 10.1021/jm034107j.

Abstract

There is compelling evidence that Bax channel activity stimulates cytochrome c release leading ultimately to cell death, which is a key event in ischemic injuries and neurodegenerative diseases. Here 3,6-dibromocarbazole piperazine derivatives of 2-propanol are described as the first small and potent modulators of the cytochrome c release triggered by Bid-induced Bax activation in a mitochondrial assay. Furthermore, a mechanism of action is proposed, and fluorescent derivatives allowing the localization of such inhibitors are reported.

摘要

有确凿证据表明,Bax通道活性会刺激细胞色素c释放,最终导致细胞死亡,这是缺血性损伤和神经退行性疾病中的关键事件。本文描述了2-丙醇的3,6-二溴咔唑哌嗪衍生物,它们是线粒体试验中由Bid诱导的Bax激活所引发的细胞色素c释放的首批小型强效调节剂。此外,还提出了一种作用机制,并报道了能使此类抑制剂定位的荧光衍生物。

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