Mingxing Teng, Ph.D.
Affiliations: | 2022- | Baylor College of Medicine, Houston, TX |
Area:
Chemical Biology, Medicinal Chemistry, Synthetic ChemistryGoogle:
"Mingxing Teng"Mean distance: (not calculated yet)
Parents
Sign in to add mentorDawei Ma | grad student | 2010-2015 | SIOC,CAS |
Martin Matzuk | post-doc | 2017-2018 | Baylor College of Medicine |
Nathanael Gray | post-doc | 2018-2022 | Dana-Farber Cancer Institute, Harvard Medical School |
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Publications
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Hassan MM, Li YD, Ma MW, et al. (2024) Exploration of the tunability of BRD4 degradation by DCAF16 trans-labelling covalent glues. European Journal of Medicinal Chemistry. 279: 116904 |
Li YD, Ma MW, Hassan MM, et al. (2024) Template-assisted covalent modification underlies activity of covalent molecular glues. Nature Chemical Biology |
Ku AF, Sharma KL, Ta HM, et al. (2024) Reversible male contraception by targeted inhibition of serine/threonine kinase 33. Science (New York, N.Y.). 384: 885-890 |
Hassan MM, Li YD, Ma MW, et al. (2023) Exploration of the Tunability of BRD4 Degradation by DCAF16 -labelling Covalent Glues. Biorxiv : the Preprint Server For Biology |
Miao Q, Kadam VD, Mukherjee A, et al. (2023) Unlocking DCAFs To Catalyze Degrader Development: An Arena for Innovative Approaches. Journal of Medicinal Chemistry. 66: 13369-13383 |
Teng M, Gray NS. (2023) The rise of degrader drugs. Cell Chemical Biology. 30: 864-878 |
Teng M, Jiang J, Wang ES, et al. (2023) Targeting the Dark Lipid Kinase PIP4K2C with a Potent and Selective Binder and Degrader. Angewandte Chemie (International Ed. in English). e202302364 |
Li YD, Ma MW, Hassan MM, et al. (2023) Template-assisted covalent modification of DCAF16 underlies activity of BRD4 molecular glue degraders. Biorxiv : the Preprint Server For Biology |
Ye Q, Belabed H, Wang Y, et al. (2022) Advancing ASMS with LC-MS/MS for the discovery of novel PDCL2 ligands from DNA-Encoded chemical library selections. Andrology |
Modukuri RK, Yu Z, Tan Z, et al. (2022) Discovery of potent BET bromodomain 1 stereoselective inhibitors using DNA-encoded chemical library selections. Proceedings of the National Academy of Sciences of the United States of America. 119: e2122506119 |