Selective inhibition of the chymotrypsin-like activity of the 20S proteasome by 5-methoxy-1-indanone dipeptide benzamides

被引:35
作者
Lum, RT [1 ]
Nelson, MG [1 ]
Joly, A [1 ]
Horsma, AG [1 ]
Lee, G [1 ]
Meyer, SM [1 ]
Wick, MM [1 ]
Schow, SR [1 ]
机构
[1] CV Therapeut Inc, Palo Alto, CA 94304 USA
关键词
D O I
10.1016/S0960-894X(98)00015-8
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Potent inhibitors of the 20S proteasome that contain a novel indanone head group coupled to di and tripeptides are described. These compounds are the first proteasome inhibitors have demonstrated high selectivity for the chymotrypsin-like activity of the 20S proteasome. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:209 / 214
页数:6
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