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抗坏血酸及其类似物对睾丸透明质酸酶和透明质酸裂解酶活性以及对透明质酸的影响。

Effects of ascorbic acid and analogs on the activity of testicular hyaluronidase and hyaluronan lyase on hyaluronan.

作者信息

Okorukwu Odilia N, Vercruysse Koen P

机构信息

Chemistry Department, Tennessee State University, 3500 John A. Merritt Blvd., Nashville, TN 37209, USA.

出版信息

J Enzyme Inhib Med Chem. 2003 Aug;18(4):377-82. doi: 10.1080/1475636031000120416.

Abstract

We have evaluated the inhibition of testicular hyaluronidase and hyaluronan lyase by L-ascorbic acid and chemical analogs. We observed that L-ascorbic acid, D-isoascorbic acid and dehydroascorbic acid inhibited both types of enzymes, but showed stronger effects towards hyaluronan lyase. But these compounds were observed to degrade the substrate, hyaluronan, by themselves. Of the other ascorbic acid analogs tested, saccharic acid inhibited hyaluronan lyase, while not affecting the enzymatic activity of testicular hyaluronidase, nor affecting the physic-chemical stability of hyaluronan. This is the first compound, to our knowledge, to be shown to possess such selective inhibition. Therefore, we propose that saccharic acid could serve as a lead compound for the development of potent and selective inhibitors of bacterial hyaluronan lyase or of polysaccharide lyase enzymes in general as we observed this compound to be capable of inhibiting chondroitinase ABC in addition to hyaluronan lyase.

摘要

我们评估了L-抗坏血酸及其化学类似物对睾丸透明质酸酶和透明质酸裂解酶的抑制作用。我们观察到,L-抗坏血酸、D-异抗坏血酸和脱氢抗坏血酸均能抑制这两种酶,但对透明质酸裂解酶的作用更强。然而,这些化合物自身会降解底物透明质酸。在所测试的其他抗坏血酸类似物中,糖二酸可抑制透明质酸裂解酶,而不影响睾丸透明质酸酶的酶活性,也不影响透明质酸的物理化学稳定性。据我们所知,这是第一种显示出具有这种选择性抑制作用的化合物。因此,我们认为糖二酸可作为一种先导化合物,用于开发强效且选择性的细菌透明质酸裂解酶抑制剂或一般多糖裂解酶抑制剂,因为我们观察到该化合物除了能抑制透明质酸裂解酶外,还能抑制软骨素酶ABC。

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