作者:Tsuyoshi Ohba、Naoki Tsuchiya、Kuniko Nishimura、Eitatsu Ikeda、Jun Wakayama、Hisashi Takei
DOI:10.1016/0960-894x(96)00065-0
日期:1996.3
The peptidyl ester derivatives of 2,2-dichlorocyclopropanol and the amide derivative of 2,2-dichlorocyclopropylamine were prepred as novel mechanism-based inactivators of alpha-chymotrypsin. The esters inactivated alpha-chymotrypsin irreversibly but the amide did not show any irreversible inhibitory activity toward alpha-chymotrypsin.