Design, synthesis and biological evaluation of tyrosinase-targeting PROTACs

被引:11
|
作者
Fu, Dingqiang [1 ,4 ]
Yuan, Yi [1 ]
Qin, Fengming [3 ]
Xu, Yan [1 ]
Cui, Xin [1 ]
Li, Guangxun [1 ]
Yao, Shaohua [3 ]
Deng, Yun [2 ]
Tang, Zhuo [1 ]
机构
[1] Chinese Acad Sci, Nat Prod Res Ctr, Chengdu Inst Biol, Chengdu 610041, Peoples R China
[2] Chengdu Univ Tradit Chinese Med, State Key Lab Southwestern Chinese Med Resources, Key Lab Standardizat Chinese Herbal Med, Minist Educ, Chengdu 611137, Peoples R China
[3] Sichuan Univ, West China Hosp, Canc Ctr, Lab Biotherapy,Natl Key Lab Biotherapy, Chengdu 610041, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金; 中国科学院西部之光基金;
关键词
Human tyrosinase; Cereblon E3 ubiquitin ligase; PROTAC; Pigmentary skin disorders; SMALL-MOLECULE; PROTEIN-DEGRADATION; ELLAGIC ACID; L-DOPA; SKIN; ZEBRAFISH; HYDROQUINONE; AGENTS; EXPRESSION; DELIVERY;
D O I
10.1016/j.ejmech.2021.113850
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The human tyrosinase is the most prominent therapeutic target for pigmentary skin disorders. However, the overwhelming majority efforts have been devoted to search mushroom tyrosinase inhibitors, which show poor inhibitory activity on human tyrosinase and certain side effects that cause skin damage in practical application. Herein, a series of degraders that directly targeted human tyrosinase was firstly designed and synthesized based on newly developed PROTAC technology. The best PROTAC TD9 induced human tyrosinase degradation obviously in dose and time-dependent manner, and its mechanism of inducing tyrosinase degradation has also been clearly demonstrated. Besides, encouraging results that low-toxicity PROTAC TD9 was applied to reduce zebrafish melanin synthesis have been obtained, highlighting the potential to treatment of tyrosinase-related disorders. Moreover, this work has innovatively expanded the application scope of PROTAC technology and laid a solid foundation for further development of novel drugs treating pigmentary skin disorders. (C) 2021 Published by Elsevier Masson SAS.
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页数:13
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