Principal Investigator
Small-Molecule Drug Research Center
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CONTACT
yjzhao@simm.ac.cn
021-50800608
201203
555 Zu Chong Zhi Road, Zhang Jiang Hi-Tech Park, Pudong, Shanghai, P.R.China
1. Modulation of protein-protein interactions with rational designed small molecules;
2. Discovery and biological activity studies of novel kinase inhibitors;
3. Modifications and medicinal chemistry studies of natural products with biological activities.
1.Discovery of a selective NIK kinase inhibitor XT2: our data show that small molecule NIK inhibitor XT2 inhibited that activation of NFκB2 signal pathway in liver cells, decreased the liver cells apoptosis induced by toxin, and prolonged the life span of mice in a liver-damage model. These results suggest that inhibition of NIK activity in vivo maybe a good therapeutic target for treating liver-damage related diseases.
2.Discovery of small molecule BY27 that blocks BET bromodomain/Histone protein-protein interactions: our data demonstrated significant differences between a selective BET BD2 inhibitor and a pan BET inhibitor, which suggest that selective BET BD2 inhibitors have potential pharmaceutical applications in clinical setting.
3.Discovery of a selective ASK1 kinase inhibitor YD57: our data show that YD57 inhibited ASK1 and several other kinases, which promoted apoptosis, induced cell cycle arrest, and had very potent activities in killing liver cancer cells.
4.Discovery of EGFR kinase inhibitors: we found that the allenamide moiety was a good bioisostere of the acrylamide group in structures of covalent EGFR inhibitors. The allenamide moiety reacted with the -SH group of a cysteine much faster than that of the acrylamide group. These data suggest the allenamide moiety could be used for labeling the -SH group of cysteines in vitro and in intact cells.
Full Publication List
Selected Publications
1.Jing Cheng, Xuexin Feng, Zhiqiang Li, Feilong Zhou, Jin-Ming Yang, Yujun Zhao*, Pharmacological inhibition of NF-κB-Inducing Kinase (NIK) with small molecules for the treatment of human diseases, RCS Medicinal Chemistry, 2021, DOI: 10.1039/d0md00361a.
2.Xuan Wang, Jiaxiang Liu, Ziqin Yan, Xiaohong Liu, Sixiu Liu, Yanrui Suo, Weiwei Lu, Jinfeng Yue, Kaixian Chen, Hualiang Jiang, Yujun Zhao*, Mingyue Zheng*, Dongcheng Dai*, Xiaojie Lu*, Diversified strategy for the synthesis of DNA-encoded oxindole libraries, Chemical Science, 2021, DOI: 10.1039/D0SC06696F.
3.Zhiqiang Li, Xinzhi Li, Ming-Bo Su, Li-Xin Gao, Yu-Bo Zhou, Bingchuan Yuan, Xilin Lyu, Ziqin Yan, Chujiao Hu, Hao Zhang, Cheng Luo, Zheng Chen*, Jia Li*, Yujun Zhao*, Discovery of a potent and selective NF-κB-inducing kinase (NIK) inhibitor that has anti-inflammatory effects in vitro and in vivo, Journal of Medicinal Chemistry, 2020, 63, 4388-4407.
4.Shiyan Zhang, Chaoying Huang, Xilin Lyu, Peipei Wang, Yi Zang, Zengtao Wang, Huan Wang, Jia Li*, Yujun Zhao*, Discovery of a 2-pyridinyl urea-containing compound YD57 as a potent inhibitor of apoptosis signal -regulating kinase 1 (ASK1), European Journal of Medicinal Chemistry, 2020, 195, 112277.
5.Deheng Chen, Tian Lu, Ziqin Yan, Wenchao Lu, Feilong Zhou, Xilin Lyu, Biling Xu, Hualiang Jiang, Kaixian Chen, Cheng Luo*, and Yujun Zhao*, Discovery, structural insight, and bioactivities of BY27 as a selective inhibitor of the second bromodomains of BET proteins, European Journal of Medicinal Chemistry, 2019, 182, 111633.
6.Erbao Zhao, Feilong Zhou, and Yujun Zhao*, Lewis Acids Promoted 3+2 Cycloaddition of Oxaziridines and Cyclic Allylic Alcohols through Carbonyl Imine Intermediates, Journal of Organic Chemistry, 2019, 84 (7), 4282–4293.
7.Deheng Chen, Dexiang Guo, Ziqin Yan, Yujun Zhao*, Allenamide as a bioisostere of acrylamide in design andsynthesis of targeted covalent inhibitors Med. Chem. Commun. 2018, 9, 244-253.
8.Feilong Zhou, Erbao Zhao, Ziqin Yan, Deheng Chen, Yujun Zhao*, Synthesis of 3,4-diarylsubstituted hexahydro-1H-indoles, Tetrahedron Letters, 2018, 59, 1871-1874.
9.Xiaomeng Ren, Xinzhi Li, Linna Jia, Deheng Chen, Hai Hou, Liangyou Rui, Yujun Zhao*, Zheng Chen*, A small-molecule inhibitor of NF-kB-inducing kinase (NIK) protects liver from toxin-induced inflammation, oxidative stress, and injury, FASEB Journal. 2017, 2, 711-718.
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