酪氨酸酶抑制剂的药物设计。

Q3 Biochemistry, Genetics and Molecular Biology
Enzymes Pub Date : 2024-01-01 Epub Date: 2024-06-25 DOI:10.1016/bs.enz.2024.06.001
Francesco Melfi, Simone Carradori, Arianna Granese, Amar Osmanović, Cristina Campestre
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引用次数: 0

摘要

这种含铜酶催化了黑色素皮肤色素生物生成的限速步骤。酪氨酸酶抑制剂可用作皮肤美白剂和食品防腐剂,为食品、化妆品、农业和医药领域开辟了新的前景。尽管存在天然抑制剂(对苯二酚、α-熊果苷、曲酸、维甲酸、壬二酸、白藜芦醇、茶杉酸、缬氨鞣、金丝桃素和苯乙基间苯二酚),但为了克服副作用和提高天然抑制剂的功效,人们提出了一些合成化合物。本章将从 MedChem 的角度收集有关合成酪氨酸酶抑制剂的最新进展,为基于支架设计创新化合物提供新的建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug design of tyrosinase inhibitors.

This copper-containing enzyme catalyzes the rate-limiting step for the melanin skin pigment bioproduction. Tyrosinase inhibitors can be exploited as skin whitening agents and food preservatives, opening new scenarios in food, cosmetics, agriculture and medicine. Despite the availability of natural inhibitors (hydroquinone, α-arbutin, kojic acid, retinoids, azelaic acid, resveratrol, caftaric acid, valonea tannin, chrysosplenetin and phenylethyl resorcinol), several synthetic compounds were proposed to overcome side effects and to improve the efficacy of natural agents. This chapter will gather the recent advances about synthetic tyrosinase inhibitors from the MedChem perspective, providing new suggestions for the scaffold-based design of innovative compounds.

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来源期刊
Enzymes
Enzymes Biochemistry, Genetics and Molecular Biology-Biotechnology
CiteScore
4.30
自引率
0.00%
发文量
10
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