Towatari T, Nikawa T, Murata M, Yokoo C, Tamai M, Hanada K, Katunuma N
Division of Enzyme Chemistry, University of Tokushima, Japan.
FEBS Lett. 1991 Mar 25;280(2):311-5. doi: 10.1016/0014-5793(91)80319-x.
New derivatives of E-64 (compound CA-030 and CA-074) were tested in vitro and in vivo for selective inhibition of cathepsin B. They exhibited 10,000-30,000 times greater inhibitory effects on purified rat cathepsin B than on cathepsin H and L: their initial Ki values for cathepsin B were about 2-5 nM, like that of E-64-c, whereas their initial Ki values for cathepsins H and L were about 40 200 microM. In in vivo conditions, such as intraperitoneal injection of compound CA-030 or CA-074 into rats, compound CA-074 is an especially potent selective inhibitor of cathepsin B, whereas compound CA-030 does not show selectivity for cathepsin B, although both compounds CA-030 and CA-074 show complete selectivity for cathepsin B in vitro.
对E-64的新衍生物(化合物CA-030和CA-074)进行了体外和体内测试,以研究其对组织蛋白酶B的选择性抑制作用。与组织蛋白酶H和L相比,它们对纯化的大鼠组织蛋白酶B的抑制作用要强10,000 - 30,000倍:它们对组织蛋白酶B的初始Ki值约为2 - 5 nM,与E-64-c相似,而它们对组织蛋白酶H和L的初始Ki值约为40 - 200 μM。在体内条件下,如向大鼠腹腔注射化合物CA-030或CA-074,化合物CA-074是一种特别有效的组织蛋白酶B选择性抑制剂,而化合物CA-030对组织蛋白酶B没有选择性,尽管化合物CA-030和CA-074在体外对组织蛋白酶B都表现出完全的选择性。