Wu K - Search Results

1

Multisubstituted quinoxalines and pyrido[2,3-d]pyrimidines: synthesis and SAR study as tyrosine kinase c-Met inhibitors.

Wu K, Ai J, Liu Q, Chen T, Zhao A, Peng X, Wang Y, Ji Y, Yao Q, Xu Y, Geng M, Zhang A. Wu K, et al. Bioorg Med Chem Lett. 2012 Oct 15;22(20):6368-72. doi: 10.1016/j.bmcl.2012.08.075. Epub 2012 Aug 27. Bioorg Med Chem Lett. 2012. PMID: 22985853

2

Discovery of novel 2,4-diarylaminopyrimidine analogues (DAAPalogues) showing potent inhibitory activities against both wild-type and mutant ALK kinases.

Song Z, Yang Y, Liu Z, Peng X, Guo J, Yang X, Wu K, Ai J, Ding J, Geng M, Zhang A. Song Z, et al. Among authors: wu k. J Med Chem. 2015 Jan 8;58(1):197-211. doi: 10.1021/jm5005144. Epub 2014 May 8. J Med Chem. 2015. PMID: 24785465

3

Novel 2,4-Diarylaminopyrimidine Analogues (DAAPalogues) Showing Potent c-Met/ALK Multikinase Inhibitory Activities.

Liu Z, Ai J, Peng X, Song Z, Wu K, Zhang J, Yao Q, Chen Y, Ji Y, Yang Y, Geng M, Zhang A. Liu Z, et al. Among authors: wu k. ACS Med Chem Lett. 2014 Feb 8;5(4):304-8. doi: 10.1021/ml400373j. eCollection 2014 Apr 10. ACS Med Chem Lett. 2014. PMID: 24900831 Free PMC article.

4

Rh(III)-catalyzed intermolecular C-H amination of 1-aryl-1H-pyrazol-5(4H)-ones with alkylamines.

Wu K, Fan Z, Xue Y, Yao Q, Zhang A. Wu K, et al. Org Lett. 2014 Jan 3;16(1):42-5. doi: 10.1021/ol402965d. Epub 2013 Dec 12. Org Lett. 2014. PMID: 24328718

5

Palladium-catalyzed double C-H activation: one-pot synthesis of benzo[c]pyrazolo[1,2-a]cinnolin-1-ones from 5-pyrazolones and aryl iodides.

Fan Z, Wu K, Xing L, Yao Q, Zhang A. Fan Z, et al. Among authors: wu k. Chem Commun (Camb). 2014 Feb 18;50(14):1682-4. doi: 10.1039/c3cc47989g. Epub 2014 Jan 6. Chem Commun (Camb). 2014. PMID: 24394189

6

Multi-Targeted Anticancer Agents.

Zheng W, Zhao Y, Luo Q, Zhang Y, Wu K, Wang F. Zheng W, et al. Among authors: wu k. Curr Top Med Chem. 2017 Nov 20;17(28):3084-3098. doi: 10.2174/1568026617666170707124126. Curr Top Med Chem. 2017. PMID: 28685693 Review.

7

Binding of Organometallic Ruthenium Anticancer Complexes to DNA: Thermodynamic Base and Sequence Selectivity.

Liu S, Liang A, Wu K, Zeng W, Luo Q, Wang F. Liu S, et al. Among authors: wu k. Int J Mol Sci. 2018 Jul 23;19(7):2137. doi: 10.3390/ijms19072137. Int J Mol Sci. 2018. PMID: 30041439 Free PMC article.

8

Discovery of a dual-targeting organometallic ruthenium complex with high activity inducing early stage apoptosis of cancer cells.

Du J, Zhang E, Zhao Y, Zheng W, Zhang Y, Lin Y, Wang Z, Luo Q, Wu K, Wang F. Du J, et al. Among authors: wu k. Metallomics. 2015 Dec;7(12):1573-83. doi: 10.1039/c5mt00122f. Metallomics. 2015. PMID: 26446567

9

Synthesis, Characterization, and in Vitro Antitumor Activity of Ruthenium(II) Polypyridyl Complexes Tethering EGFR-Inhibiting 4-Anilinoquinazolines.

Du J, Kang Y, Zhao Y, Zheng W, Zhang Y, Lin Y, Wang Z, Wang Y, Luo Q, Wu K, Wang F. Du J, et al. Among authors: wu k. Inorg Chem. 2016 May 2;55(9):4595-605. doi: 10.1021/acs.inorgchem.6b00309. Epub 2016 Apr 19. Inorg Chem. 2016. PMID: 27093574

10

Arene control over thiolate to sulfinate oxidation in albumin by organometallic ruthenium anticancer complexes.

Hu W, Luo Q, Ma X, Wu K, Liu J, Chen Y, Xiong S, Wang J, Sadler PJ, Wang F. Hu W, et al. Among authors: wu k. Chemistry. 2009 Jul 6;15(27):6586-94. doi: 10.1002/chem.200900699. Chemistry. 2009. PMID: 19533706

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