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具有非编码氨基酸的三肽作为潜在的丝氨酸蛋白酶抑制剂。

Tripeptides with non-code amino acids as potential serine proteases inhibitors.

机构信息

Department of Organic Chemistry, Poland.

出版信息

J Enzyme Inhib Med Chem. 2013 Jun;28(3):639-43. doi: 10.3109/14756366.2011.651463. Epub 2012 Feb 3.

Abstract

Eight peptides of the general H-D-Ser-AA-Arg-OH formula, where AA = phenylglycine, phenylalanine, homophenylalanine, cyclohexylglycine, cyclohexylalanine, homocyclohexylalanine, α-methylphenylalanine and 1-aminocyclohexyl carboxylic acid were obtained and tested for their effect on the amidolytic activities of urokinase, thrombin, trypsin, plasmin, t-PA and kallikrein. We tested the hemolytic activity of the peptides against porcine erythrocytes and the antitumor activity against the human breast cancer cells, standard MCF-7 and estrogen-independent MDA-MB-231. The most active compounds were H-D-Ser-Chg-Arg-OH towards thrombin and H-D-Ser-Phg-Arg-OH towards plasmin with K(i) value 5.02 μM and 5.7 μM, respectively.

摘要

得到了 8 个通式为 H-D-Ser-AA-Arg-OH 的肽,其中 AA = 苯丙氨酸、苯甘氨酸、高苯丙氨酸、环己基甘氨酸、环己基丙氨酸、高环己基丙氨酸、α-甲基苯丙氨酸和 1-氨基环己烷羧酸,并测试了它们对尿激酶、凝血酶、胰蛋白酶、纤溶酶、t-PA 和激肽释放酶的 amidolytic 活性的影响。我们测试了肽对猪红细胞的溶血活性以及对人乳腺癌细胞(标准 MCF-7 和雌激素非依赖性 MDA-MB-231)的抗肿瘤活性。最活跃的化合物是 H-D-Ser-Chg-Arg-OH 对凝血酶,H-D-Ser-Phg-Arg-OH 对纤溶酶,其 K(i) 值分别为 5.02 μM 和 5.7 μM。

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