Zhao D - Search Results

1

Identification of 1H-pyrazolo[3,4-b]pyridine derivatives as novel and potent TBK1 inhibitors: design, synthesis, biological evaluation, and molecular docking study.

Sun Y, Tang H, Wang X, Feng F, Fan T, Zhao D, Xiong B, Xie H, Liu T. Sun Y, et al. Among authors: zhao d. J Enzyme Inhib Med Chem. 2022 Dec;37(1):1411-1425. doi: 10.1080/14756366.2022.2076674. J Enzyme Inhib Med Chem. 2022. PMID: 35587686 Free PMC article.

2

Synthesis and biological evaluation of 4α/4β-imidazolyl podophyllotoxin analogues as antitumor agents.

Shang H, Chen H, Zhao D, Tang X, Liu Y, Pan L, Cheng M. Shang H, et al. Among authors: zhao d. Arch Pharm (Weinheim). 2012 Jan;345(1):43-8. doi: 10.1002/ardp.201100094. Epub 2011 Sep 28. Arch Pharm (Weinheim). 2012. PMID: 21956645

3

Energetic factors determining the binding of type I inhibitors to c-Met kinase: experimental studies and quantum mechanical calculations.

Yu Z, Ma YC, Ai J, Chen DQ, Zhao DM, Wang X, Chen YL, Geng MY, Xiong B, Cheng MS, Shen JK. Yu Z, et al. Acta Pharmacol Sin. 2013 Nov;34(11):1475-83. doi: 10.1038/aps.2013.85. Epub 2013 Sep 23. Acta Pharmacol Sin. 2013. PMID: 24056705 Free PMC article.

4

Synthesis and biological evaluation of 3-phenyl-3-aryl carboxamido propanoic acid derivatives as small molecule inhibitors of retinoic acid 4-hydroxylase (CYP26A1).

Zhao D, Sun B, Ren J, Li F, Song S, Lv X, Hao C, Cheng M. Zhao D, et al. Bioorg Med Chem. 2015 Mar 15;23(6):1356-65. doi: 10.1016/j.bmc.2014.11.036. Epub 2015 Jan 21. Bioorg Med Chem. 2015. PMID: 25684424

5

Design, synthesis and biological evaluation of 1-phenanthryl-tetrahydroisoquinoline derivatives as novel p21-activated kinase 4 (PAK4) inhibitors.

Song S, Li X, Guo J, Hao C, Feng Y, Guo B, Liu T, Zhang Q, Zhang Z, Li R, Wang J, Lin B, Li F, Zhao D, Cheng M. Song S, et al. Among authors: zhao d. Org Biomol Chem. 2015 Mar 28;13(12):3803-18. doi: 10.1039/c5ob00037h. Org Biomol Chem. 2015. PMID: 25705811

6

Design, synthesis, and biological evaluation of amide imidazole derivatives as novel metabolic enzyme CYP26A1 inhibitors.

Sun B, Liu K, Han J, Zhao LY, Su X, Lin B, Zhao DM, Cheng MS. Sun B, et al. Bioorg Med Chem. 2015 Oct 15;23(20):6763-73. doi: 10.1016/j.bmc.2015.08.019. Epub 2015 Aug 20. Bioorg Med Chem. 2015. PMID: 26365710

7

Design, Synthesis and Biological Evaluation of Novel Substituted N,N'-Diaryl ureas as Potent p38 Inhibitors.

Zhu D, Li X, Zhong W, Zhao D. Zhu D, et al. Among authors: zhao d. Molecules. 2015 Sep 11;20(9):16604-19. doi: 10.3390/molecules200916604. Molecules. 2015. PMID: 26378516 Free PMC article.

8

Discovery of novel N,N-3-phenyl-3-benzylaminopropionanilides as potent inhibitors of cholesteryl ester transfer protein in vivo.

Xie H, Li Y, Bai C, Wang R, Liu C, Hao C, Lin B, Cheng M, Zhao D. Xie H, et al. Among authors: zhao d. Bioorg Med Chem. 2016 Apr 15;24(8):1811-8. doi: 10.1016/j.bmc.2016.03.002. Epub 2016 Mar 2. Bioorg Med Chem. 2016. PMID: 26993745

9

Design, synthesis and biological evaluation of N,N-3-phenyl-3-benzylaminopropanamide derivatives as novel cholesteryl ester transfer protein inhibitor.

Zhao D, Xie H, Bai C, Liu C, Hao C, Zhao S, Yuan H, Luo C, Wang J, Lin B, Zheng J, Cheng M. Zhao D, et al. Among authors: zhao s. Bioorg Med Chem. 2016 Apr 15;24(8):1589-97. doi: 10.1016/j.bmc.2015.12.010. Epub 2015 Dec 8. Bioorg Med Chem. 2016. PMID: 27010500

10

Discovery of a new series of imidazo[1,2-a]pyridine compounds as selective c-Met inhibitors.

Liu TC, Peng X, Ma YC, Ji YC, Chen DQ, Zheng MY, Zhao DM, Cheng MS, Geng MY, Shen JK, Ai J, Xiong B. Liu TC, et al. Acta Pharmacol Sin. 2016 May;37(5):698-707. doi: 10.1038/aps.2016.11. Epub 2016 Apr 4. Acta Pharmacol Sin. 2016. PMID: 27041462 Free PMC article.

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