Wei W - Search Results

1

Design, synthesis and biological evaluation of 1H-pyrrolo[2,3-b]pyridine derivatives as potent fibroblast growth factor receptor inhibitors.

Su X, Liu Z, Yue L, Wu X, Wei W, Que H, Ye T, Luo Y, Zhang Y. Su X, et al. Among authors: wei w. RSC Adv. 2021 Jun 9;11(34):20651-20661. doi: 10.1039/d1ra02660g. eCollection 2021 Jun 9. RSC Adv. 2021. PMID: 35479379 Free PMC article.

2

Synthesis and biological evaluation of indazole derivatives as anti-cancer agents.

Wei W, Liu Z, Wu X, Gan C, Su X, Liu H, Que H, Zhang Q, Xue Q, Yue L, Yu L, Ye T. Wei W, et al. RSC Adv. 2021 Apr 27;11(26):15675-15687. doi: 10.1039/d1ra01147b. eCollection 2021 Apr 26. RSC Adv. 2021. PMID: 35481216 Free PMC article.

3

Design, synthesis and biological evaluation of a series of novel pyrrolo[2,3-d]pyrimidin/pyrazolo[3,4-d]pyrimidin-4-amine derivatives as FGFRs-dominant multi-target receptor tyrosine kinase inhibitors for the treatment of gastric cancer.

Wu X, Liu Z, Gan C, Wei W, Zhang Q, Liu H, Que H, Su X, Yue L, He H, Ouyang L, Ye T. Wu X, et al. Among authors: wei w. Bioorg Chem. 2022 Oct;127:105965. doi: 10.1016/j.bioorg.2022.105965. Epub 2022 Jun 14. Bioorg Chem. 2022. PMID: 35759882

4

A novel multikinase inhibitor SKLB-YTH-60 ameliorates inflammation and fibrosis in bleomycin-induced lung fibrosis mouse models.

Liu H, Wu X, Gan C, Wang L, Wang G, Yue L, Liu Z, Wei W, Su X, Zhang Q, Tan Z, Yao Y, Ouyang L, Yu L, Ye T. Liu H, et al. Among authors: wei w. Cell Prolif. 2021 Jul;54(7):e13081. doi: 10.1111/cpr.13081. Epub 2021 Jun 14. Cell Prolif. 2021. PMID: 34121240 Free PMC article.

5

Design, synthesis and biological evaluation of 7-((7H-pyrrolo[2,3-d]pyrimidin-4-yl)oxy)-2,3-dihydro-1H-inden-1-one derivatives as potent FAK inhibitors for the treatment of ovarian cancer.

Wei W, Feng Z, Liu Z, Li X, He H, Ran K, Shi Y, Zhu Y, Ye T, Gao C, Wang N, Yu L. Wei W, et al. Eur J Med Chem. 2022 Jan 15;228:113978. doi: 10.1016/j.ejmech.2021.113978. Epub 2021 Nov 11. Eur J Med Chem. 2022. PMID: 34810020

6

Design and Synthesis of EZH2-Based PROTACs to Degrade the PRC2 Complex for Targeting the Noncatalytic Activity of EZH2.

Liu Z, Hu X, Wang Q, Wu X, Zhang Q, Wei W, Su X, He H, Zhou S, Hu R, Ye T, Zhu Y, Wang N, Yu L. Liu Z, et al. Among authors: wei w. J Med Chem. 2021 Mar 11;64(5):2829-2848. doi: 10.1021/acs.jmedchem.0c02234. Epub 2021 Feb 19. J Med Chem. 2021. PMID: 33606537

7

Small Molecule TH-39 Potentially Targets Hec1/Nek2 Interaction and Exhibits Antitumor Efficacy in K562 Cells via G0/G1 Cell Cycle Arrest and Apoptosis Induction.

Zhu Y, Wei W, Ye T, Liu Z, Liu L, Luo Y, Zhang L, Gao C, Wang N, Yu L. Zhu Y, et al. Among authors: wei w. Cell Physiol Biochem. 2016;40(1-2):297-308. doi: 10.1159/000452546. Epub 2016 Nov 18. Cell Physiol Biochem. 2016. PMID: 27855372 Free article.

8

YLT-11, a novel PLK4 inhibitor, inhibits human breast cancer growth via inducing maladjusted centriole duplication and mitotic defect.

Lei Q, Xiong L, Xia Y, Feng Z, Gao T, Wei W, Song X, Ye T, Wang N, Peng C, Li Z, Liu Z, Yu L. Lei Q, et al. Among authors: wei w. Cell Death Dis. 2018 Oct 18;9(11):1066. doi: 10.1038/s41419-018-1071-2. Cell Death Dis. 2018. PMID: 30337519 Free PMC article.

9

Design, synthesis and biological evaluations of a series of Pyrido[1,2-a]pyrimidinone derivatives as novel selective FGFR inhibitors.

Ran K, Zeng J, Wan G, He X, Feng Z, Xiang W, Wei W, Hu X, Wang N, Liu Z, Yu L. Ran K, et al. Among authors: wei w. Eur J Med Chem. 2021 Aug 5;220:113499. doi: 10.1016/j.ejmech.2021.113499. Epub 2021 Apr 26. Eur J Med Chem. 2021. PMID: 33940465

10

Identification of novel 2-aminothiazole conjugated nitrofuran as antitubercular and antibacterial agents.

Ran K, Gao C, Deng H, Lei Q, You X, Wang N, Shi Y, Liu Z, Wei W, Peng C, Xiong L, Xiao K, Yu L. Ran K, et al. Among authors: wei w. Bioorg Med Chem Lett. 2016 Aug 1;26(15):3669-74. doi: 10.1016/j.bmcl.2016.05.088. Epub 2016 May 30. Bioorg Med Chem Lett. 2016. PMID: 27289321

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