Ke Ding, Ph.D

Affiliations: 
1991-1998 China Pharmaceutical University 
 1998-2001 Fudan university, Shanghai, Shanghai Shi, China 
 2006-2016 Guangzhou Institutes Biomedicine and Health,CAS 
 2016- Jinan University 
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"Ke Ding"
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Publications

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Liu W, Bai Y, Zhou L, et al. (2023) Discovery of LWY713 as a potent and selective FLT3 PROTAC degrader with in vivo activity against acute myeloid leukemia. European Journal of Medicinal Chemistry. 264: 115974
Zhang H, Lin G, Jia S, et al. (2023) Discovery and optimization of thieno[3,2-d]pyrimidine derivatives as highly selective inhibitors of cyclin-dependent kinase 7. European Journal of Medicinal Chemistry. 263: 115955
Li C, Qiao Y, Jiang X, et al. (2023) Discovery of a First-in-Class Degrader for the Lipid Kinase PIKfyve. Journal of Medicinal Chemistry
Wei Y, Xu X, Jiang M, et al. (2023) Discovery of new Lenalidomide derivatives as potent and selective GSPT1 degraders. European Journal of Medicinal Chemistry. 258: 115580
He R, Song Z, Bai Y, et al. (2023) Discovery of AXL Degraders with Improved Potencies in Triple-Negative Breast Cancer (TNBC) Cells. Journal of Medicinal Chemistry
Chan S, Zhang Y, Wang J, et al. (2022) Discovery of 3-Aminopyrazole Derivatives as New Potent and Orally Bioavailable AXL Inhibitors. Journal of Medicinal Chemistry
Zhang Y, Chan S, He R, et al. (2022) 1-Methyl-3-((4-(quinolin-4-yloxy)phenyl)amino)-1H-pyrazole-4-carboxamide derivatives as new rearranged during Transfection (RET) kinase inhibitors capable of suppressing resistant mutants in solvent-front regions. European Journal of Medicinal Chemistry. 244: 114862
Li S, Zhang P, Xu F, et al. (2022) Ynamide Electrophile for the Profiling of Ligandable Carboxyl Residues in Live Cells and the Development of New Covalent Inhibitors. Journal of Medicinal Chemistry
Lu J, Huang Y, Huang J, et al. (2022) Discovery of the First Examples of Threonine Tyrosine Kinase PROTAC Degraders. Journal of Medicinal Chemistry
Zhang YH, Li YF, Wang Y, et al. (2020) Identification and characterization of N9-methyltransferase involved in converting caffeine into non-stimulatory theacrine in tea. Nature Communications. 11: 1473
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