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胰蛋白酶、纤溶酶、激肽释放酶、凝血酶、C1r和C1酯酶的合成抑制剂。

Synthetic inhibitors of trypsin, plasmin, kallikrein, thrombin, C1r-, and C1 esterase.

作者信息

Tamura Y, Hirado M, Okamura K, Minato Y, Fujii S

出版信息

Biochim Biophys Acta. 1977 Oct 13;484(2):417-22. doi: 10.1016/0005-2744(77)90097-3.

Abstract

p-Carbethoxyphenyl episol-guanidinocaproate and p-(p'-guanidinobenzoyloxy)-phenyl derivatives were prepared, and their inhibitory effects on trypsin, plasmin, plasma kallikrein, thrombin, C1r- and C1 esterase were examined. Among the various inhibitors tested, p-nitrophenyl p'-guanidinobenzoate, N,N-dimethylamino p-(p'-guanidinobenzoyloxy)-benzoyl glycolate and N,N-dimethylamino p-(p'-guanidinobenzoyloxy)-benzilcarbonyloxy glycolate were the most effective inhibitors of trypsin, plasmin, plasma kallikrien and thrombin, and they strongly inhibited the esterolytic activities of C1r- and C1 esterase.

摘要

制备了对 - 乙氧羰基苯基表高胍基己酸酯和对 -(对'-胍基苯甲酰氧基)- 苯基衍生物,并检测了它们对胰蛋白酶、纤溶酶、血浆激肽释放酶、凝血酶、C1r 和 C1 酯酶的抑制作用。在所测试的各种抑制剂中,对硝基苯基对'-胍基苯甲酸酯、N,N - 二甲基氨基对 -(对'-胍基苯甲酰氧基)- 苯甲酰乙醇酸酯和 N,N - 二甲基氨基对 -(对'-胍基苯甲酰氧基)- 二苯甲酰羰基氧基乙醇酸酯是胰蛋白酶、纤溶酶、血浆激肽释放酶和凝血酶最有效的抑制剂,并且它们强烈抑制 C1r 和 C1 酯酶的酯解活性。

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