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- 介绍: E-64是一个不可逆的,强有力的,高选择性半胱氨酸蛋白酶抑制剂。E-64不和非蛋白酶的官能硫基基团发生反应,如L-乳酸脱氢酶或肌酸激酶。 E-64像其他半胱氨酸蛋白酶抑制剂一样,如亮肽素和抗痛素,不会抑制丝氨酸蛋白酶(胰蛋白酶除外)。E-64的反式-环氧丁二酰基(活性部分)不可逆地结合在许多的半胱氨酸蛋白酶的活性巯基基团,如木瓜蛋白酶,猕猴桃酶(actinidase),组织蛋白酶B,H,和L。 E-64是一种体内研究非常有用的半胱氨酸蛋白酶抑制剂,因为它有专一性的抑制特点,它可渗透到细胞和组织中,并具有低毒性。
- 比重: 1·44
- 储存条件: -20℃
- 用途: E-64是一种亲和纯化半胱氨酸蛋白酶的有效配体。当耦合到硫基化的亲和基质时,结合不再是不可逆的,但保留特异性
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