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酚类化合物的超氧阴离子自由基清除活性。

Superoxide radical scavenging activity of phenolic compounds.

作者信息

Tsujimoto Y, Hashizume H, Yamazaki M

机构信息

Department of Endodontics, Nihon University School of Dentistry at Matsudo, Chiba, Japan.

出版信息

Int J Biochem. 1993 Apr;25(4):491-4. doi: 10.1016/0020-711x(93)90655-x.

DOI:10.1016/0020-711x(93)90655-x
PMID:8385635
Abstract
  1. Superoxide radicals (O2-.) were generated from a hypoxanthin-xanthin oxidase (HPX-XOD) reaction system and detected by the electron spin resonance (ESR) spin-trapping technique. 2. The inhibitory effect on O2-. generation occurred in the order: superoxide dismutase (SOD) > L-ascorbic acid > eugenol > guaiacol > phenol. 3. And the second-order rate constants between O2-. and samples were: SOD 1.7 x 10(9)/M/S, L-ascorbic acid 3.4 x 10(5)/M/S, eugenol 8.3 x 10(3)/M/S, guaiacol 2.5 x 10(3)/M/S and phenol 5.8 x 10(2)/M/S. 4. It was clarified that the phenolic compounds have O2-. scavenging activity.
摘要
  1. 超氧阴离子自由基(O2-.)由次黄嘌呤 - 黄嘌呤氧化酶(HPX - XOD)反应系统产生,并通过电子自旋共振(ESR)自旋捕获技术进行检测。2. 对O2-.生成的抑制作用顺序为:超氧化物歧化酶(SOD)> L - 抗坏血酸>丁香酚>愈创木酚>苯酚。3. O2-.与样品之间的二级反应速率常数分别为:SOD 1.7×10(9)/M/S,L - 抗坏血酸3.4×10(5)/M/S,丁香酚8.3×10(3)/M/S,愈创木酚2.5×10(3)/M/S,苯酚5.8×10(2)/M/S。4. 已阐明酚类化合物具有O2-.清除活性。

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