Wang X - Search Results

1

Inhibition of DDR1 promotes ferroptosis and overcomes gefitinib resistance in non-small cell lung cancer.

Zhang Y, Qian J, Fu Y, Wang Z, Hu W, Zhang J, Wang Y, Guo Y, Chen W, Zhang Y, Wang X, Xie Z, Ye H, Ye F, Zuo Z. Zhang Y, et al. Among authors: wang x, wang z, wang y. Biochim Biophys Acta Mol Basis Dis. 2024 Oct;1870(7):167447. doi: 10.1016/j.bbadis.2024.167447. Epub 2024 Jul 30. Biochim Biophys Acta Mol Basis Dis. 2024. PMID: 39089636

2

Synthesis and Evaluation of Biological and Antitumor Activities of Tetrahydrobenzothieno[2,3-d]Pyrimidine Derivatives as Novel Inhibitors of FGFR1.

Wang X, Chen D, Yu S, Zhang Z, Wang Y, Qi X, Fu W, Xie Z, Ye F. Wang X, et al. Among authors: wang y. Chem Biol Drug Des. 2016 Apr;87(4):499-507. doi: 10.1111/cbdd.12687. Epub 2016 Feb 1. Chem Biol Drug Des. 2016. PMID: 26575787

3

Synthesis and Evaluation of Phenylxanthine Derivatives as Potential Dual A2AR Antagonists/MAO-B Inhibitors for Parkinson's Disease.

Wang X, Han C, Xu Y, Wu K, Chen S, Hu M, Wang L, Ye Y, Ye F. Wang X, et al. Among authors: wang l. Molecules. 2017 Jun 17;22(6):1010. doi: 10.3390/molecules22061010. Molecules. 2017. PMID: 28629145 Free PMC article.

4

Design, Synthesis, and Biological Evaluation of C-2 Substituted 3Hthieno[ 2,3-d]pyrimidin-4-one Derivatives as Novel FGFR1 Inhibitors.

Guo P, Xie Z, Zhang H, Zhang Z, Han C, Cheng D, Lin D, Zhang Y, Wang X, Guo X, Ye F. Guo P, et al. Among authors: wang x. Med Chem. 2017;13(8):753-760. doi: 10.2174/1573406413666170623084525. Med Chem. 2017. PMID: 28641527

5

Design, synthesis and ability of non-gold complexed substituted purine derivatives to inhibit LPS-induced inflammatory response.

Wang X, Han C, Wu K, Luo L, Wang Y, Du X, He Q, Ye F. Wang X, et al. Among authors: wang y. Eur J Med Chem. 2018 Apr 10;149:10-21. doi: 10.1016/j.ejmech.2018.02.018. Epub 2018 Feb 10. Eur J Med Chem. 2018. PMID: 29494841

6

Design, synthesis and biological evaluation of 4-bromo-N-(3,5-dimethoxyphenyl)benzamide derivatives as novel FGFR1 inhibitors for treatment of non-small cell lung cancer.

Xie Z, Cheng D, Luo L, Shen G, Pan S, Pan Y, Chen B, Wang X, Liu Z, Zhang Y, Ye F. Xie Z, et al. Among authors: wang x. J Enzyme Inhib Med Chem. 2018 Dec;33(1):905-919. doi: 10.1080/14756366.2018.1460824. J Enzyme Inhib Med Chem. 2018. PMID: 29734851 Free PMC article.

7

Design, synthesis and activity of novel 2,6-disubstituted purine derivatives, potential small molecule inhibitors of signal transducer and activator of transcription 3.

Wang X, He Q, Wu K, Guo T, Du X, Zhang H, Fang L, Zheng N, Zhang Q, Ye F. Wang X, et al. Eur J Med Chem. 2019 Oct 1;179:218-232. doi: 10.1016/j.ejmech.2019.06.017. Epub 2019 Jun 21. Eur J Med Chem. 2019. PMID: 31254923

8

Discovery of 4,6-pyrimidinediamine derivatives as novel dual EGFR/FGFR inhibitors aimed EGFR/FGFR1-positive NSCLC.

Xie Z, Wu K, Wang Y, Pan Y, Chen B, Cheng D, Pan S, Guo T, Du X, Fang L, Wang X, Ye F. Xie Z, et al. Among authors: wang x, wang y. Eur J Med Chem. 2020 Feb 1;187:111943. doi: 10.1016/j.ejmech.2019.111943. Epub 2019 Dec 5. Eur J Med Chem. 2020. PMID: 31846829

9

Discovery of N-substituted sulfamoylbenzamide derivatives as novel inhibitors of STAT3 signaling pathway based on Niclosamide.

Wang X, Wu K, Fang L, Yang X, Zheng N, Du Z, Lu Y, Xie Z, Liu Z, Zuo Z, Ye F. Wang X, et al. Eur J Med Chem. 2021 Jun 5;218:113362. doi: 10.1016/j.ejmech.2021.113362. Epub 2021 Mar 17. Eur J Med Chem. 2021. PMID: 33774344

10

Discovery of 4-methoxy-N-(1-naphthyl)benzenesulfonamide derivatives as small molecule dual-target inhibitors of tubulin and signal transducer and activator of transcription 3 (STAT3) based on ABT-751.

Wang X, Lu Y, Sun D, Qian J, Tu S, Yue W, Lin H, Tang H, Meng F, He Q, Xie Z, Zhang Y, Chen H, Ma S, Zuo Z, Ye F. Wang X, et al. Bioorg Chem. 2022 Aug;125:105864. doi: 10.1016/j.bioorg.2022.105864. Epub 2022 May 10. Bioorg Chem. 2022. PMID: 35584606

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