Stürzebecher J
Acta Biol Med Ger. 1981;40(10-11):1519-22.
Acrosin proved to be very susceptible to inhibition by benzamidine derivatives. Most of the inhibitors were at least 10-fold more potent against acrosin than against trypsin. The most potent inhibitors of acrosin of this series were amidinophenyl compounds with a keto group or a carbon amide moiety in the side chain. Comparison of the structure-activity relationships for the inhibition of acrosin and trypsin showed differences in the binding sites of both enzymes.
事实证明,顶体蛋白酶极易受到苯甲脒衍生物的抑制。大多数抑制剂对顶体蛋白酶的抑制效力比对胰蛋白酶的抑制效力至少高10倍。该系列中对顶体蛋白酶最有效的抑制剂是侧链带有酮基或碳酰胺部分的脒基苯基化合物。对顶体蛋白酶和胰蛋白酶抑制作用的构效关系比较表明,这两种酶的结合位点存在差异。