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苯乙基间苯二酚抑制黑色素形成的机理研究

郝谜谜 王艳 刘园园 鲍炎 李红艳 郑琳

日用化学工业2018,Vol.48Issue(5):293-298,6.
日用化学工业2018,Vol.48Issue(5):293-298,6.DOI:10.13218/j.cnki.csdc.2018.05.010

苯乙基间苯二酚抑制黑色素形成的机理研究

Study on the mechanism of inhibition of melanin by phenethyl resorcinol

郝谜谜 1王艳 1刘园园 1鲍炎 2李红艳 3郑琳1

作者信息

  • 1. 天津中医药大学,天津 300193
  • 2. 天津市口腔医院(南开大学口腔医院),天津 300041
  • 3. 天津嘉氏堂科技有限公司,天津 300457
  • 折叠

摘要

Abstract

Using the drug substitution method, the two stages in the process of melanin formation (i. e. enzyme catalysis and nonenzymatic catalysis) were blocked, in order to explore the mechanism of inhibition of melanin formation by phenethyl resorcinol. Using L-tyrosine and L-DOPA as substrates, after the reaction at 37 ℃ in the phosphate buffer solution of pH = 6. 8, the absorbance was measured at 475 nm. The effect of phenethyl resorcinol on the catalytic reaction of tyrosinase was studied, and the inhibition kinetic parameters were calculated;The mechanism of inhibition of tyrosinase by phenethyl resorcinol was explored by molecular docking analysis. Results show that phenethyl resorcinol is a tyrosinase inhibitor which can inhibit the enzymic catalytic reaction in the process of melanin formation, while it has no effect on nonenzymatic catalysis;phenethyl resorcinol can efficiently inhibit the activities of monophenolase and diphenolase of tyrosinase, with 50% inhibiting concentrations being 0. 28 and 31 μmol/L, respectively;it is found that the inhibition of diphenolase is noncompetitive, and the inhibition constant is Km = 1. 1;molecular docking results show that phenethyl resorcinol forms hydrogen bonds with tyrosinase MET A: 280, accompanied by hydrophobic interaction.

关键词

美白化妆品添加剂/苯乙基间苯二酚/酪氨酸酶/动力学/分子对接

Key words

whitening cosmetic additive/phenethyl resorcinol/tyrosinase/kinetics/molecular docking

分类

化学化工

引用本文复制引用

郝谜谜,王艳,刘园园,鲍炎,李红艳,郑琳..苯乙基间苯二酚抑制黑色素形成的机理研究[J].日用化学工业,2018,48(5):293-298,6.

基金项目

国家自然科学基金资助项目(81602773) (81602773)

日用化学工业

OA北大核心CSCDCSTPCD

1001-1803

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