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
  • [21] Design and Evaluation of PROTACs Targeting Acyl Protein Thioesterase 1
    Carvalho, Luis A. R.
    Sousa, Barbara B.
    Zaidman, Daniel
    Kiely-Collins, Hannah
    Bernardes, Goncalo J. L.
    CHEMBIOCHEM, 2024, 25 (04)
  • [22] Design, synthesis, and biological evaluation of multiple targeting antimalarials
    Yiqing Yang
    Tongke Tang
    Xiaolu Li
    Thomas Michel
    Liqin Ling
    Zhenghui Huang
    Maruthi Mulaka
    Yue Wu
    Hongying Gao
    Liguo Wang
    Jing Zhou
    Brigitte Meunier
    Hangjun Ke
    Lubin Jiang
    Yu Rao
    Acta Pharmaceutica Sinica B, 2021, 11 (09) : 2900 - 2913
  • [23] Design, synthesis, and biological evaluation of multiple targeting antimalarials
    Yang, Yiqing
    Tang, Tongke
    Li, Xiaolu
    Michel, Thomas
    Ling, Liqin
    Huang, Zhenghui
    Mulaka, Maruthi
    Wu, Yue
    Gao, Hongying
    Wang, Liguo
    Zhou, Jing
    Meunier, Brigitte
    Ke, Hangjun
    Jiang, Lubin
    Rao, Yu
    ACTA PHARMACEUTICA SINICA B, 2021, 11 (09) : 2900 - 2913
  • [24] Design, synthesis, and biological evaluation of symmetrical azine derivatives as novel tyrosinase inhibitors
    Karimian, Somaye
    Kazemi, Fatemeh
    Attarroshan, Mahshid
    Gholampour, Maryam
    Hemmati, Shiva
    Sakhteman, Amirhossein
    Behzadipour, Yasaman
    Kabiri, Maryam
    Iraji, Aida
    Khoshneviszadeh, Mehdi
    BMC CHEMISTRY, 2021, 15 (01)
  • [25] Design, synthesis, and biological evaluation of symmetrical azine derivatives as novel tyrosinase inhibitors
    Somaye Karimian
    Fatemeh Kazemi
    Mahshid Attarroshan
    Maryam Gholampour
    Shiva Hemmati
    Amirhossein Sakhteman
    Yasaman Behzadipour
    Maryam Kabiri
    Aida Iraji
    Mehdi Khoshneviszadeh
    BMC Chemistry, 15
  • [26] Synthesis and biological evaluation of olanzapine-based PROTACs targeting human D-aspartate oxidase (hDASPO)
    Citarella, A.
    Cavinato, M.
    Rabattoni, V.
    Shehi, H.
    Galli, M.
    Nardini, M.
    Silvani, A.
    Pollegioni, L.
    Passarella, D.
    FEBS OPEN BIO, 2024, 14 : 55 - 55
  • [27] Design, synthesis and biological evaluation of mitochondria targeting theranostic agents
    Wu, Song
    Cao, Qizhen
    Wang, Xiaolin
    Cheng, Kai
    Cheng, Zhen
    CHEMICAL COMMUNICATIONS, 2014, 50 (64) : 8919 - 8922
  • [28] Design, synthesis, and biological evaluation of novel protopanoxadiol derivatives based PROTACs technology for the treatment of lung cancer
    Wang, Peng
    Zhu, Huajian
    Liu, Jianmin
    Xie, Shaowen
    Xu, Shengtao
    Chen, Yu
    Xu, Jing
    Zhao, Yuqing
    Zhu, Zheying
    Xu, Jinyi
    BIOORGANIC CHEMISTRY, 2023, 131
  • [29] Design, synthesis and evaluation of EZH2-based PROTACs targeting PRC2 complex in lymphoma
    Xie, Huiru
    Xu, Wei
    Liang, Jing
    Liu, Yang
    Zhuo, Chenxi
    Zou, Xiaoxue
    Luo, Weihong
    Xiao, Jianping
    Lin, Yu
    Chen, Lixia
    Li, Hua
    BIOORGANIC CHEMISTRY, 2023, 140
  • [30] Design, synthesis and biological evaluation of ezrin inhibitors targeting metastatic osteosarcoma
    Paige, Mikell
    Kosturko, George
    Bulut, Gullay
    Miessau, Matthew
    Rahim, Said
    Toretsky, Jeffrey A.
    Brown, Milton L.
    Ueren, Aykut
    BIOORGANIC & MEDICINAL CHEMISTRY, 2014, 22 (01) : 478 - 487