Yang W - Search Results

1

Design, synthesis and biological evaluation of 4-anilinothieno[2,3-d]pyrimidine-based hydroxamic acid derivatives as novel histone deacetylase inhibitors.

Yang W, Li L, Ji X, Wu X, Su M, Sheng L, Zang Y, Li J, Liu H. Yang W, et al. Bioorg Med Chem. 2014 Nov 1;22(21):6146-55. doi: 10.1016/j.bmc.2014.08.030. Epub 2014 Sep 4. Bioorg Med Chem. 2014. PMID: 25261927

2

Design, synthesis and biological evaluation of novel 4-anilinoquinazolines with C-6 urea-linked side chains as inhibitors of the epidermal growth factor receptor.

Zhang X, Peng T, Ji X, Li J, Tong L, Li Z, Yang W, Xu Y, Li M, Ding J, Jiang H, Xie H, Liu H. Zhang X, et al. Among authors: yang w. Bioorg Med Chem. 2013 Dec 15;21(24):7988-98. doi: 10.1016/j.bmc.2013.09.049. Epub 2013 Oct 2. Bioorg Med Chem. 2013. PMID: 24183742

3

Design, synthesis and biological evaluation of novel 6-alkenylamides substituted of 4-anilinothieno[2,3-d]pyrimidines as irreversible epidermal growth factor receptor inhibitors.

Ji X, Peng T, Zhang X, Li J, Yang W, Tong L, Qu R, Jiang H, Ding J, Xie H, Liu H. Ji X, et al. Among authors: yang w. Bioorg Med Chem. 2014 Apr 1;22(7):2366-78. doi: 10.1016/j.bmc.2014.01.035. Epub 2014 Jan 31. Bioorg Med Chem. 2014. PMID: 24565969

4

Design, synthesis and biological evaluation of isoquinoline-based derivatives as novel histone deacetylase inhibitors.

Yang W, Li L, Wang Y, Wu X, Li T, Yang N, Su M, Sheng L, Zheng M, Zang Y, Li J, Liu H. Yang W, et al. Among authors: yang n. Bioorg Med Chem. 2015 Sep 1;23(17):5881-90. doi: 10.1016/j.bmc.2015.06.071. Epub 2015 Jul 4. Bioorg Med Chem. 2015. PMID: 26211462

5

Design, synthesis and biological evaluation of thienopyrimidine hydroxamic acid based derivatives as structurally novel histone deacetylase (HDAC) inhibitors.

Wang J, Su M, Li T, Gao A, Yang W, Sheng L, Zang Y, Li J, Liu H. Wang J, et al. Among authors: yang w. Eur J Med Chem. 2017 Mar 10;128:293-299. doi: 10.1016/j.ejmech.2017.01.035. Epub 2017 Jan 23. Eur J Med Chem. 2017. PMID: 28213282

6

FeCl3 promoted highly regioselective [3 + 2] cycloaddition of dimethyl 2-vinyl and aryl cyclopropane-1,1-dicarboxylates with aryl isothiocyanates.

Wang H, Yang W, Liu H, Wang W, Li H. Wang H, et al. Among authors: yang w. Org Biomol Chem. 2012 Jul 14;10(26):5032-5. doi: 10.1039/c2ob25682g. Epub 2012 May 31. Org Biomol Chem. 2012. PMID: 22647999

7

Efficient synthesis of highly substituted pyrroles through a Pd(OCOCF3)2-catalyzed cascade reaction of 2-alkenal-1,3-dicarbonyl compounds with primary amines.

Yang W, Huang L, Liu H, Wang W, Li H. Yang W, et al. Chem Commun (Camb). 2013 May 21;49(41):4667-9. doi: 10.1039/c3cc42216j. Epub 2013 Apr 15. Chem Commun (Camb). 2013. PMID: 23584213

8

Palladium-catalyzed difunctionalization of alkynes via C-N and S-N cleavages: a versatile approach to highly functional indoles.

Zhao F, Zhang D, Nian Y, Zhang L, Yang W, Liu H. Zhao F, et al. Among authors: yang w. Org Lett. 2014 Oct 3;16(19):5124-7. doi: 10.1021/ol5024745. Epub 2014 Sep 23. Org Lett. 2014. PMID: 25248124

9

Potential anti-gout constituents as xanthine oxidase inhibitor from the fruits of Stauntonia brachyanthera.

Liu D, Wang D, Yang W, Meng D. Liu D, et al. Among authors: yang w. Bioorg Med Chem. 2017 Jul 1;25(13):3562-3566. doi: 10.1016/j.bmc.2017.05.010. Epub 2017 May 6. Bioorg Med Chem. 2017. PMID: 28511908

10

Identification of 5-(2,3-Dihydro-1 H-indol-5-yl)-7 H-pyrrolo[2,3- d]pyrimidin-4-amine Derivatives as a New Class of Receptor-Interacting Protein Kinase 1 (RIPK1) Inhibitors, Which Showed Potent Activity in a Tumor Metastasis Model.

Li Y, Xiong Y, Zhang G, Zhang L, Yang W, Yang J, Huang L, Qiao Z, Miao Z, Lin G, Sun Q, Niu T, Chen L, Niu D, Li L, Yang S. Li Y, et al. Among authors: yang s, yang w, yang j. J Med Chem. 2018 Dec 27;61(24):11398-11414. doi: 10.1021/acs.jmedchem.8b01652. Epub 2018 Dec 10. J Med Chem. 2018. PMID: 30480444

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