Design and discovery of mushroom tyrosinase inhibitors and their therapeutic applications

被引:54
作者
Mendes, Eduarda [1 ]
Perry, Maria de Jesus [2 ]
Francisco, Ana Paula [2 ]
机构
[1] Univ Lisbon, Fac Farm, Dept Toxicol & Bromatol Sci, Inst Invest Med iMed ULisboa, P-1649003 Lisbon, Portugal
[2] Univ Lisbon, Fac Farm, Dept Pharmaceut Chem & Therapeut, Inst Invest Med iMed ULisboa, P-1649003 Lisbon, Portugal
关键词
inhibitors; polyphenol oxidase; structure-activity relationship; tyrosinase; whitening agents; CINNAMIC ACID-DERIVATIVES; P-COUMARIC ACID; SUICIDE-INACTIVATION; IN-VITRO; BIOLOGICAL EVALUATION; AZO-RESVERATROL; MELANOGENESIS; ANALOGS; MECHANISM; MELANIN;
D O I
10.1517/17460441.2014.907789
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Tyrosinase inhibitors could have a huge importance in medicine, cosmetics and agriculture. Although many tyrosinase inhibitors are available, they have demonstrated only mild efficacy and safety concerns. This has led to the discovery of novel tyrosinase inhibitors that are more safe, potent and efficacious. Areas covered: The authors provide an overview of the recent scientific accounts describing the design of new molecules. These compounds belong to different chemical families. The review emphasizes the rationale behind the discovery, the study of structure-activity relationships, the study of the mechanism and kinetic of inhibition and the cellular effect of the inhibitors. The article is based on the literature published from 2007 onward related with the development of synthetic tyrosinase inhibitors. Expert opinion: Although a great number of tyrosinase inhibitors have been published in the literature, none, as of yet, have reached the potency and safety requirements needed to enter clinical trials. The emergence of new in vitro and in vivo tests will finally allow the arrival of new compounds that are more potent and safe.
引用
收藏
页码:533 / 554
页数:22
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