Mitochondrial-targeted Hsp90 C-terminal inhibitors manifest anti-proliferative activity

被引:12
|
作者
Zhang, Zheng [1 ]
Banerjee, Monimoy [1 ]
Davis, Rachel E. [1 ]
Blagg, Brian S. J. [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, 251 Nieuwland Sci Hall, Notre Dame, IN 46556 USA
基金
美国国家卫生研究院;
关键词
Hsp90 C-terminal inhibitor; Novobiocin; Triphenylphosphonium; Anticancer; NOVOBIOCIN SCAFFOLD; MODULATION; DESIGN; DERIVATIVES; ANALOGS;
D O I
10.1016/j.bmcl.2019.126676
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The development of C-terminal heat shock protein 90 kDa (Hsp90) inhibitors has emerged as a potential treatment for cancer. Similarly, small molecules that target the mitochondria have proven to be efficacious towards cancer, as the reprogramming of mitochondrial function is often associated with oncogenic transformation. Herein, we report the development of triphenylphosphonium (TPP)-conjugated Hsp90 C-terminal inhibitors, their anti-proliferative activity, and accumulation in the mitochondria. In general, TPP-conjugated Hsp90 C-terminal inhibitors were found to manifest increased activity against various cancer cell lines when compared to the parent compounds.
引用
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页数:4
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