Ma Y - Search Results

1

Discovery of 3H-imidazo[4,5-b]pyridines as potent c-Met kinase inhibitors: design, synthesis, and biological evaluation.

Chen D, Wang Y, Ma Y, Xiong B, Ai J, Chen Y, Geng M, Shen J. Chen D, et al. Among authors: ma y. ChemMedChem. 2012 Jun;7(6):1057-70. doi: 10.1002/cmdc.201200120. Epub 2012 May 13. ChemMedChem. 2012. PMID: 22581753

2

Energetic factors determining the binding of type I inhibitors to c-Met kinase: experimental studies and quantum mechanical calculations.

Yu Z, Ma YC, Ai J, Chen DQ, Zhao DM, Wang X, Chen YL, Geng MY, Xiong B, Cheng MS, Shen JK. Yu Z, et al. Acta Pharmacol Sin. 2013 Nov;34(11):1475-83. doi: 10.1038/aps.2013.85. Epub 2013 Sep 23. Acta Pharmacol Sin. 2013. PMID: 24056705 Free PMC article.

3

Discovery of a new series of imidazo[1,2-a]pyridine compounds as selective c-Met inhibitors.

Liu TC, Peng X, Ma YC, Ji YC, Chen DQ, Zheng MY, Zhao DM, Cheng MS, Geng MY, Shen JK, Ai J, Xiong B. Liu TC, et al. Acta Pharmacol Sin. 2016 May;37(5):698-707. doi: 10.1038/aps.2016.11. Epub 2016 Apr 4. Acta Pharmacol Sin. 2016. PMID: 27041462 Free PMC article.

4

Design and optimization of a series of 1-sulfonylpyrazolo[4,3-b]pyridines as selective c-Met inhibitors.

Ma Y, Sun G, Chen D, Peng X, Chen YL, Su Y, Ji Y, Liang J, Wang X, Chen L, Ding J, Xiong B, Ai J, Geng M, Shen J. Ma Y, et al. J Med Chem. 2015 Mar 12;58(5):2513-29. doi: 10.1021/jm502018y. Epub 2015 Feb 25. J Med Chem. 2015. PMID: 25668160

5

Design, Synthesis and Biological Evaluation of 6-(2,6-Dichloro-3,5-dimethoxyphenyl)-4-substituted-1H-indazoles as Potent Fibroblast Growth Factor Receptor Inhibitors.

Zhang Z, Zhao D, Dai Y, Cheng M, Geng M, Shen J, Ma Y, Ai J, Xiong B. Zhang Z, et al. Among authors: ma y. Molecules. 2016 Oct 23;21(10):1407. doi: 10.3390/molecules21101407. Molecules. 2016. PMID: 27782099 Free PMC article.

6

Discovery and Biological Evaluation of a Series of Pyrrolo[2,3-b]pyrazines as Novel FGFR Inhibitors.

Zhang Y, Liu H, Zhang Z, Wang R, Liu T, Wang C, Ma Y, Ai J, Zhao D, Shen J, Xiong B. Zhang Y, et al. Among authors: ma y. Molecules. 2017 Apr 5;22(4):583. doi: 10.3390/molecules22040583. Molecules. 2017. PMID: 28379191 Free PMC article.

7

Preclinical Evaluation of SCC244 (Glumetinib), a Novel, Potent, and Highly Selective Inhibitor of c-Met in MET-dependent Cancer Models.

Ai J, Chen Y, Peng X, Ji Y, Xi Y, Shen Y, Yang X, Su Y, Sun Y, Gao Y, Ma Y, Xiong B, Shen J, Ding J, Geng M. Ai J, et al. Among authors: ma y. Mol Cancer Ther. 2018 Apr;17(4):751-762. doi: 10.1158/1535-7163.MCT-17-0368. Epub 2017 Dec 13. Mol Cancer Ther. 2018. PMID: 29237805

8

Structure-Based Discovery of a Series of 5H-Pyrrolo[2,3-b]pyrazine FGFR Kinase Inhibitors.

Jiang A, Liu Q, Wang R, Wei P, Dai Y, Wang X, Xu Y, Ma Y, Ai J, Shen J, Ding J, Xiong B. Jiang A, et al. Among authors: ma y. Molecules. 2018 Mar 19;23(3):698. doi: 10.3390/molecules23030698. Molecules. 2018. PMID: 29562726 Free PMC article.

9

Discovery of a series of dimethoxybenzene FGFR inhibitors with 5H-pyrrolo[2,3-b]pyrazine scaffold: structure-activity relationship, crystal structural characterization and in vivo study.

Wei P, Liu B, Wang R, Gao Y, Li L, Ma Y, Qian Z, Chen Y, Cheng M, Geng M, Shen J, Zhao D, Ai J, Xiong B. Wei P, et al. Among authors: ma y. Acta Pharm Sin B. 2019 Mar;9(2):351-368. doi: 10.1016/j.apsb.2018.12.008. Epub 2018 Dec 26. Acta Pharm Sin B. 2019. PMID: 30972282 Free PMC article.

10

Ultrafine fiber-mediated transvascular interventional photothermal therapy using indocyanine green for precision embolization treatment.

Ma Y, Xiao J, Chen GJ, Dang H, Zhang Y, He X, Shum PP, Guo Q. Ma Y, et al. Biomater Sci. 2025 Jan 20. doi: 10.1039/d4bm01592d. Online ahead of print. Biomater Sci. 2025. PMID: 39831816

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