INACTIVATION OF CALPAIN BY PEPTIDYL FLUOROMETHYL KETONES

被引:61
作者
ANGLIKER, H [1 ]
ANAGLI, J [1 ]
SHAW, E [1 ]
机构
[1] FRIEDRICH MIESCHER INST, POB 2543, CH-4002 BASEL, SWITZERLAND
关键词
D O I
10.1021/jm00080a003
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The syntheses of Z-Leu-Leu-Tyr-CH2F (1) and Z-Tyr-Ala-CH2F (3) are described. The ability of Z-Leu-Leu-Tyr-CH2F (1) and Z-Leu-Tyr-CH2F (2) to inactivate in vitro calcium-activated proteinase from chicken gizzard are compared. Like the analogous diazomethyl ketones 4 and 5, these inhibitors were also found to inactivate cathepsin L in common with other inhibitors under current investigation. However, other specific inactivators for cathepsin L are available, for example, the fluoromethyl ketone 3 and diazomethyl ketone 6 of Z-Tyr-Ala-OH, which have no effect on the calcium-activated proteinase and therefore provide control inhibitors for observations made with Z-Leu-Leu-Tyr-CH2F (1).
引用
收藏
页码:216 / 220
页数:5
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