Liu N - Search Results

1

Imidazolone-amide bridges and their effects on tubulin polymerization in cis-locked vinylogous combretastatin-A4 analogues: synthesis and biological evaluation.

Li YW, Liu J, Liu N, Shi D, Zhou XT, Lv JG, Zhu J, Zheng CH, Zhou YJ. Li YW, et al. Among authors: liu j, liu n. Bioorg Med Chem. 2011 Jun 1;19(11):3579-84. doi: 10.1016/j.bmc.2011.03.068. Epub 2011 Apr 3. Bioorg Med Chem. 2011. PMID: 21536450

2

[Comparative molecular field analysis (CoMFA) of allylamine antimycotics].

Ji HT, Zhang WN, Zhou YJ, Lu JG, Li K, Zhu J, Liu N. Ji HT, et al. Among authors: liu n. Yao Xue Xue Bao. 1997 Aug;32(8):593-9. Yao Xue Xue Bao. 1997. PMID: 11596308 Chinese.

3

[Comparative molecular field analysis(CoMFA) of allylamine and benzylamine antimycotics].

Ji H, Zhang W, Zhou Y, Lu J, Zhu J, Li K, Chen W, Liu N. Ji H, et al. Among authors: liu n. Yao Xue Xue Bao. 1998;33(3):188-93. Yao Xue Xue Bao. 1998. PMID: 11938964 Chinese.

4

Synthesis and biological evaluation of 1-phenyl-1,2,3,4-dihydroisoquinoline compounds as tubulin polymerization inhibitors.

Zheng CH, Chen J, Liu J, Zhou XT, Liu N, Shi D, Huang JJ, Lv JG, Zhu J, Zhou YJ. Zheng CH, et al. Among authors: liu j, liu n. Arch Pharm (Weinheim). 2012 Jun;345(6):454-62. doi: 10.1002/ardp.201100169. Epub 2012 Mar 13. Arch Pharm (Weinheim). 2012. PMID: 22415658

5

Physicochemical property-driven optimization of diarylaniline compounds as potent HIV-1 non-nucleoside reverse transcriptase inhibitors.

Liu N, Qin B, Sun LQ, Yu F, Lu L, Jiang S, Lee KH, Xie L. Liu N, et al. Bioorg Med Chem Lett. 2014 Aug 15;24(16):3719-23. doi: 10.1016/j.bmcl.2014.07.011. Epub 2014 Jul 11. Bioorg Med Chem Lett. 2014. PMID: 25042339 Free PMC article.

6

Discovery of (2-benzoylethen-1-ol)-containing 1,2-benzothiazine derivatives as novel 4-hydroxyphenylpyruvate dioxygenase (HPPD) inhibiting-based herbicide lead compounds.

Lei K, Hua XW, Tao YY, Liu Y, Liu N, Ma Y, Li YH, Xu XH, Kong CH. Lei K, et al. Among authors: liu y, liu n. Bioorg Med Chem. 2016 Jan 15;24(2):92-103. doi: 10.1016/j.bmc.2015.11.032. Epub 2015 Nov 25. Bioorg Med Chem. 2016. PMID: 26682702

7

Design, synthesis and biological evaluation of benzo[cd]indol-2(1H)-ones derivatives as BRD4 inhibitors.

Feng Y, Xiao S, Chen Y, Jiang H, Liu N, Luo C, Chen S, Chen H. Feng Y, et al. Among authors: liu n. Eur J Med Chem. 2018 May 25;152:264-273. doi: 10.1016/j.ejmech.2018.04.048. Epub 2018 Apr 28. Eur J Med Chem. 2018. PMID: 29730189

8

Design, synthesis and anti leukemia cells proliferation activities of pyrimidylaminoquinoline derivatives as DOT1L inhibitors.

Zhang L, Chen Y, Liu N, Li L, Xiao S, Li X, Chen K, Luo C, Chen S, Chen H. Zhang L, et al. Among authors: liu n. Bioorg Chem. 2018 Oct;80:649-654. doi: 10.1016/j.bioorg.2018.07.022. Epub 2018 Jul 21. Bioorg Chem. 2018. PMID: 30059890

9

Design, synthesis and biological evaluation of 2-aminopyridine derivatives as USP7 inhibitors.

Xu X, Wang M, Xu H, Liu N, Chen K, Luo C, Chen S, Chen H. Xu X, et al. Among authors: liu n. Bioorg Chem. 2022 Dec;129:106128. doi: 10.1016/j.bioorg.2022.106128. Epub 2022 Sep 10. Bioorg Chem. 2022. PMID: 36113266

10

Scaffold hopping of sampangine: discovery of potent antifungal lead compound against Aspergillus fumigatus and Cryptococcus neoformans.

Jiang Z, Liu N, Dong G, Jiang Y, Liu Y, He X, Huang Y, He S, Chen W, Li Z, Yao J, Miao Z, Zhang W, Sheng C. Jiang Z, et al. Among authors: liu y, liu n. Bioorg Med Chem Lett. 2014 Sep 1;24(17):4090-4. doi: 10.1016/j.bmcl.2014.07.064. Epub 2014 Aug 1. Bioorg Med Chem Lett. 2014. PMID: 25115626

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