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.
引用
收藏
页数:13
相关论文
共 50 条
  • [1] Design, synthesis, and biological evaluation of RIPK1-targeting PROTACs
    Zhang, Hefeng
    Zhang, Shuonan
    Wang, Tianchen
    Lan, Yaohan
    Dai, Yang
    Peng, Xia
    An, Yuxiang
    Xue, Yi
    Ai, Jing
    Duan, Wenhu
    MOLECULAR DIVERSITY, 2025,
  • [2] Design, Synthesis, and Biological Evaluation of IRAK4-Targeting PROTACs
    Chen, Yun
    Ning, Yi
    Bai, Gang
    Tong, Linjiang
    Zhang, Tao
    Zhou, Jinpei
    Zhang, Huibin
    Xie, Hua
    Ding, Jian
    Duan, Wenhu
    ACS MEDICINAL CHEMISTRY LETTERS, 2021, 12 (01): : 82 - 87
  • [3] Design, Synthesis, and Biological Evaluation of MEK PROTACs
    Vollmer, Stefan
    Cunoosamy, Danen
    Lv, Huafei
    Feng, Huanxi
    Li, Xia
    Nan, Ziyang
    Yang, Wenzhen
    Perry, Matthew W. D.
    JOURNAL OF MEDICINAL CHEMISTRY, 2020, 63 (01) : 157 - 162
  • [4] Design, synthesis and biological evaluation of MNK-PROTACs
    Sun, Xue
    Wu, Qingyun
    Bu, Hong
    Pei, Yifeng
    Guan, Dezhong
    Guo, Shi
    Zhou, Jinpei
    Zhang, Huibin
    MOLECULAR DIVERSITY, 2024, 28 (06) : 3783 - 3800
  • [5] Design, Synthesis, and Evaluation of BCL-2 Targeting PROTACs
    Bricelj, Alesa
    Ng, Yuen Lam Dora
    Gobec, Martina
    Kuchta, Robert
    Hu, Wanyi
    Javornik, Spela
    Rozic, Miha
    Guetschow, Michael
    Zheng, Guangrong
    Kroenke, Jan
    Steinebach, Christian
    Sosic, Izidor
    CHEMISTRY-A EUROPEAN JOURNAL, 2024, 30 (45)
  • [6] Design, synthesis, and biological evaluation of novel BTK-targeting proteolysis targeting chimeras (PROTACs) with enhanced pharmacokinetic properties
    Lin, Ying
    Liu, Jing
    Tian, Xinjian
    Wang, Jin
    Su, Huahua
    Xiang, Jianpin
    Cao, Tao
    Wang, Yonghui
    Xie, Qiong
    Yu, Xufen
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2025, 289
  • [7] Design, Synthesis, and Biological Evaluation of mTOR-Targeting PROTACs Based on MLN0128 and Pomalidomide
    Zhang, Qi
    Yan, Peizheng
    Zhao, Pan
    Zhao, Dongsheng
    Cao, Heran
    Lu, Jing
    Mao, Beibei
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2023, 71 (02) : 120 - 128
  • [8] Design, Synthesis, and Biological Evaluation of Novel EGFR PROTACs Targeting C797S Mutation
    Zhu, Yasheng
    Ye, Xiuquan
    Wu, Yuxing
    Shen, Hao
    Cai, Zeyu
    Xia, Fei
    Min, Wenjian
    Hou, Yi
    Wang, Liping
    Wang, Xiao
    Xiao, Yibei
    Yang, Peng
    JOURNAL OF MEDICINAL CHEMISTRY, 2024, 67 (09) : 7283 - 7300
  • [9] Design, synthesis and biological evaluation of Proteolysis Targeting Chimeras (PROTACs) as a BTK degraders with improved pharmacokinetic properties
    Jaime-Figueroa, Saul
    Buhimschi, Alexandru D.
    Toure, Momar
    Hines, John
    Crews, Craig M.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2020, 30 (03)
  • [10] Design, Synthesis, and Evaluation of Highly Potent FAK-Targeting PROTACs
    Gao, Hongying
    Wu, Yue
    Sun, Yonghui
    Yang, Yiqing
    Zhou, Guangbiao
    Rao, Yu
    ACS MEDICINAL CHEMISTRY LETTERS, 2020, 11 (10): : 1855 - 1862