Jiang C - Search Results

1

Design, synthesis and anti-inflammatory evaluation of 3-amide benzoic acid derivatives as novel P2Y₁₄ receptor antagonists.

Zhang Z, Hao K, Li H, Lu R, Liu C, Zhou M, Li B, Meng Z, Hu Q, Jiang C. Zhang Z, et al. Among authors: jiang c. Eur J Med Chem. 2019 Nov 1;181:111564. doi: 10.1016/j.ejmech.2019.111564. Epub 2019 Jul 26. Eur J Med Chem. 2019. PMID: 31376563

2

Discovery of tetrahydro-beta-carbolines as inhibitors of the mitotic kinesin KSP.

Liu F, Yu LQ, Jiang C, Yang L, Wu WT, You QD. Liu F, et al. Among authors: jiang c. Bioorg Med Chem. 2010 Jun 15;18(12):4167-77. doi: 10.1016/j.bmc.2010.05.024. Epub 2010 May 11. Bioorg Med Chem. 2010. PMID: 20537544

3

Design, synthesis and bioevaluation of dihydropyrazolo[3,4-b]pyridine and benzo[4,5]imidazo[1,2-a]pyrimidine compounds as dual KSP and Aurora-A kinase inhibitors for anti-cancer agents.

Fu RG, You QD, Yang L, Wu WT, Jiang C, Xu XL. Fu RG, et al. Among authors: jiang c. Bioorg Med Chem. 2010 Nov 15;18(22):8035-43. doi: 10.1016/j.bmc.2010.09.020. Epub 2010 Sep 16. Bioorg Med Chem. 2010. PMID: 20934346

4

De novo design, synthesis and biological evaluation of 1,4-dihydroquinolin-4-ones and 1,2,3,4-tetrahydroquinazolin-4-ones as potent kinesin spindle protein (KSP) inhibitors.

Jiang C, Yang L, Wu WT, Guo QL, You QD. Jiang C, et al. Bioorg Med Chem. 2011 Sep 15;19(18):5612-27. doi: 10.1016/j.bmc.2011.07.029. Epub 2011 Jul 22. Bioorg Med Chem. 2011. PMID: 21856161

5

Synthesis and evaluation of gambogic acid derivatives as antitumor agents. Part III.

Guo XK, Sun HP, Shen S, Sun Y, Xie FL, Tao L, Guo QL, Jiang C, You QD. Guo XK, et al. Among authors: jiang c. Chem Biodivers. 2013 Jan;10(1):73-85. doi: 10.1002/cbdv.201200126. Chem Biodivers. 2013. PMID: 23341209

6

Design, synthesis, and evaluation of non-ATP-competitive small-molecule Polo-like kinase 1 (Plk1) inhibitors.

Chen DX, Huang J, Liu M, Xu YG, Jiang C. Chen DX, et al. Among authors: jiang c. Arch Pharm (Weinheim). 2015 Jan;348(1):2-9. doi: 10.1002/ardp.201400294. Epub 2014 Nov 27. Arch Pharm (Weinheim). 2015. PMID: 25430493

7

Identification of indole-3-carboxylic acids as non-ATP-competitive Polo-like kinase 1 (Plk1) inhibitors.

Liu M, Huang J, Chen DX, Jiang C. Liu M, et al. Among authors: jiang c. Bioorg Med Chem Lett. 2015 Feb 1;25(3):431-4. doi: 10.1016/j.bmcl.2014.12.060. Epub 2014 Dec 24. Bioorg Med Chem Lett. 2015. PMID: 25556101

8

Design, synthesis and docking studies of novel dipeptidyl boronic acid proteasome inhibitors constructed from αα- and αβ-amino acids.

Shi J, Lei M, Wu W, Feng H, Wang J, Chen S, Zhu Y, Hu S, Liu Z, Jiang C. Shi J, et al. Among authors: jiang c. Bioorg Med Chem Lett. 2016 Apr 15;26(8):1958-62. doi: 10.1016/j.bmcl.2016.03.007. Epub 2016 Mar 3. Bioorg Med Chem Lett. 2016. PMID: 26965867

9

Design, synthesis and biological evaluation of phosphopeptides as Polo-like kinase 1 Polo-box domain inhibitors.

Lin TY, Min HP, Jiang C, Niu MM, Yan F, Xu LL, Di B. Lin TY, et al. Among authors: jiang c. Bioorg Med Chem. 2018 Jul 23;26(12):3429-3437. doi: 10.1016/j.bmc.2018.05.014. Epub 2018 May 14. Bioorg Med Chem. 2018. PMID: 29807699

10

Identification of novel and selective non-peptide inhibitors targeting the polo-box domain of polo-like kinase 1.

Chen Y, Li Z, Liu Y, Lin T, Sun H, Yang D, Jiang C. Chen Y, et al. Among authors: jiang c. Bioorg Chem. 2018 Dec;81:278-288. doi: 10.1016/j.bioorg.2018.08.030. Epub 2018 Aug 23. Bioorg Chem. 2018. PMID: 30170276

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