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拉德斯特,一种新型的热休克蛋白90(Hsp90)蛋白质折叠机制抑制剂。

Radester, a novel inhibitor of the Hsp90 protein folding machinery.

作者信息

Shen Gang, Blagg Brian S J

机构信息

Department of Medicinal Chemistry and The Center for Protein Structure and Function, The University of Kansas, 1251 Wescoe Hall Drive, Malott 4070, Lawrence, Kansas 66045-7562, USA.

出版信息

Org Lett. 2005 May 26;7(11):2157-60. doi: 10.1021/ol050580a.

Abstract

[reaction: see text]. The antitumor antibiotics radicicol and geldanamycin are potent inhibitors of the Hsp90 protein folding machinery. Radester is a hybrid composed of radicicol's resorcinol ring and geldanamycin's quinone through an isopropyl ester. Radester was prepared, and the cytotoxicity of it and the corresponding hydroquinone were determined in MCF-7 breast cancer cells to be 13.9 and 7.1 microM, respectively. Protein degradation assays were performed on Hsp90-dependent client proteins, Her-2 and Raf, to correlate Hsp90 inhibition to cytotoxicity.

摘要

[反应:见正文]。抗肿瘤抗生素雷地西醇和格尔德霉素是热休克蛋白90(Hsp90)蛋白质折叠机制的有效抑制剂。雷地司特是一种通过异丙酯将雷地西醇的间苯二酚环与格尔德霉素的醌连接而成的杂合物。制备了雷地司特,并测定其及相应对苯二酚在MCF-7乳腺癌细胞中的细胞毒性分别为13.9和7.1微摩尔。对Hsp90依赖性客户蛋白Her-2和Raf进行了蛋白质降解试验,以将Hsp90抑制与细胞毒性相关联。

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