Gao J - Search Results

1

Design, synthesis, and biological evaluation of novel 4-anilinoquinazoline derivatives bearing amino acid moiety as potential EGFR kinase inhibitors.

Zheng YG, Su J, Gao CY, Jiang P, An L, Xue YS, Gao J, Liu Y. Zheng YG, et al. Among authors: gao j, gao cy. Eur J Med Chem. 2017 Apr 21;130:393-405. doi: 10.1016/j.ejmech.2017.02.061. Epub 2017 Feb 28. Eur J Med Chem. 2017. PMID: 28279846

2

Synthesis, Biological Evaluation and Molecular Docking Studies of Piperidinylpiperidines and Spirochromanones Possessing Quinoline Moieties as Acetyl-CoA Carboxylase Inhibitors.

Huang T, Sun J, Wang Q, Gao J, Liu Y. Huang T, et al. Among authors: gao j. Molecules. 2015 Sep 7;20(9):16221-34. doi: 10.3390/molecules200916221. Molecules. 2015. PMID: 26370948 Free PMC article.

3

Structure-Based Drug Design of Small Molecule Peptide Deformylase Inhibitors to Treat Cancer.

Gao J, Wang T, Qiu S, Zhu Y, Liang L, Zheng Y. Gao J, et al. Molecules. 2016 Mar 23;21(4):396. doi: 10.3390/molecules21040396. Molecules. 2016. PMID: 27023495 Free PMC article.

4

Design, Synthesis, and Biological Evaluation of Vanillin Hydroxamic Acid Derivatives as Novel Peptide Deformylase Inhibitors.

Gao J, Qiu S, Liang L, Hao Z, Zhou Q, Wang F, Mou J, Lin Q. Gao J, et al. Curr Comput Aided Drug Des. 2018;14(1):95-101. doi: 10.2174/1573409913666170613074601. Curr Comput Aided Drug Des. 2018. PMID: 28606047

5

Identification of Direct Activator of Adenosine Monophosphate-Activated Protein Kinase (AMPK) by Structure-Based Virtual Screening and Molecular Docking Approach.

Huang T, Sun J, Zhou S, Gao J, Liu Y. Huang T, et al. Among authors: gao j. Int J Mol Sci. 2017 Jun 30;18(7):1408. doi: 10.3390/ijms18071408. Int J Mol Sci. 2017. PMID: 28665353 Free PMC article.

6

Design and synthesis of a novel photoaffinity probe for labelling EGF receptor tyrosine kinases.

Zheng YG, Wu XQ, Su J, Jiang P, Xu L, Gao J, Cai B, Ji M. Zheng YG, et al. Among authors: gao j. J Enzyme Inhib Med Chem. 2017 Dec;32(1):954-959. doi: 10.1080/14756366.2017.1344979. J Enzyme Inhib Med Chem. 2017. PMID: 28718674 Free PMC article.

7

Design, synthesis and evaluation of novel phenyl propionamide derivatives as non-nucleoside hepatitis B virus inhibitors.

Qiu J, Gong Q, Gao J, Chen W, Zhang Y, Gu X, Tang D. Qiu J, et al. Among authors: gao j. Eur J Med Chem. 2018 Jan 20;144:424-434. doi: 10.1016/j.ejmech.2017.12.042. Epub 2017 Dec 16. Eur J Med Chem. 2018. PMID: 29288943

8

A novel galactose-PEG-conjugated biodegradable copolymer is an efficient gene delivery vector for immunotherapy of hepatocellular carcinoma.

Liu L, Zong ZM, Liu Q, Jiang SS, Zhang Q, Cen LQ, Gao J, Gao XG, Huang JD, Liu Y, Yao H. Liu L, et al. Among authors: gao j, gao xg. Biomaterials. 2018 Nov;184:20-30. doi: 10.1016/j.biomaterials.2018.08.064. Epub 2018 Sep 1. Biomaterials. 2018. PMID: 30195802

9

Assessment of quinazolinone derivatives as novel non-nucleoside hepatitis B virus inhibitors.

Qiu J, Chen W, Zhang Y, Zhou Q, Chen J, Yang L, Gao J, Gu X, Tang D. Qiu J, et al. Among authors: gao j. Eur J Med Chem. 2019 Aug 15;176:41-49. doi: 10.1016/j.ejmech.2019.05.014. Epub 2019 May 7. Eur J Med Chem. 2019. PMID: 31091479

10

An oral 2-hydroxypropyl-β-cyclodextrin-loaded spirooxindole-pyrrolizidine derivative restores p53 activity via targeting MDM2 and JNK1/2 in hepatocellular carcinoma.

Gao X, Wei M, Shan W, Liu Q, Gao J, Liu Y, Zhu S, Yao H. Gao X, et al. Among authors: gao j. Pharmacol Res. 2019 Oct;148:104400. doi: 10.1016/j.phrs.2019.104400. Epub 2019 Aug 16. Pharmacol Res. 2019. PMID: 31425749

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