Liu ZJ - Search Results

1

Synthesis and antimicrobical evaluation of a novel class of 1,3,4-thiadiazole: derivatives bearing 1,2,4-triazolo[1,5-a]pyrimidine moiety.

Luo Y, Zhang S, Liu ZJ, Chen W, Fu J, Zeng QF, Zhu HL. Luo Y, et al. Among authors: liu zj. Eur J Med Chem. 2013 Jun;64:54-61. doi: 10.1016/j.ejmech.2013.04.014. Epub 2013 Apr 15. Eur J Med Chem. 2013. PMID: 23644188

2

Design, synthesis, and biological evaluation of chalcone oxime derivatives as potential immunosuppressive agents.

Luo Y, Song R, Li Y, Zhang S, Liu ZJ, Fu J, Zhu HL. Luo Y, et al. Among authors: liu zj. Bioorg Med Chem Lett. 2012 May 1;22(9):3039-43. doi: 10.1016/j.bmcl.2012.03.080. Epub 2012 Mar 28. Bioorg Med Chem Lett. 2012. PMID: 22494616

3

Synthesis, biological evaluation and molecular docking studies of novel 2-(1,3,4-oxadiazol-2-ylthio)-1-phenylethanone derivatives.

Zhang LR, Liu ZJ, Zhang H, Sun J, Luo Y, Zhao TT, Gong HB, Zhu HL. Zhang LR, et al. Among authors: liu zj. Bioorg Med Chem. 2012 Jun 1;20(11):3615-21. doi: 10.1016/j.bmc.2012.03.061. Epub 2012 Apr 11. Bioorg Med Chem. 2012. PMID: 22541051

4

Design, synthesis and antimicrobial activities of nitroimidazole derivatives containing 1,3,4-oxadiazole scaffold as FabH inhibitors.

Li Y, Luo Y, Hu Y, Zhu DD, Zhang S, Liu ZJ, Gong HB, Zhu HL. Li Y, et al. Among authors: liu zj. Bioorg Med Chem. 2012 Jul 15;20(14):4316-22. doi: 10.1016/j.bmc.2012.05.050. Epub 2012 May 30. Bioorg Med Chem. 2012. PMID: 22710102

5

Synthesis, biological evaluation, 3D-QSAR studies of novel aryl-2H-pyrazole derivatives as telomerase inhibitors.

Luo Y, Zhang S, Qiu KM, Liu ZJ, Yang YS, Fu J, Zhong WQ, Zhu HL. Luo Y, et al. Among authors: liu zj. Bioorg Med Chem Lett. 2013 Feb 15;23(4):1091-5. doi: 10.1016/j.bmcl.2012.12.010. Epub 2012 Dec 20. Bioorg Med Chem Lett. 2013. PMID: 23312949

6

Synthesis, biological evaluation, and molecular docking studies of novel 1,3,4-oxadiazole derivatives possessing benzotriazole moiety as FAK inhibitors with anticancer activity.

Zhang S, Luo Y, He LQ, Liu ZJ, Jiang AQ, Yang YH, Zhu HL. Zhang S, et al. Among authors: liu zj. Bioorg Med Chem. 2013 Jul 1;21(13):3723-9. doi: 10.1016/j.bmc.2013.04.043. Epub 2013 Apr 23. Bioorg Med Chem. 2013. PMID: 23673215

7

DMXAA-pyranoxanthone hybrids enhance inhibition activities against human cancer cells with multi-target functions.

Liu J, Zhou F, Zhang L, Wang H, Zhang J, Zhang C, Jiang Z, Li Y, Liu Z, Chen H. Liu J, et al. Eur J Med Chem. 2018 Jan 1;143:1768-1778. doi: 10.1016/j.ejmech.2017.10.074. Epub 2017 Oct 31. Eur J Med Chem. 2018. PMID: 29129511

8

A novel and practical route to A-ring enyne synthon for 1 alpha,25-dihydroxyvitamin D3 analogs: synthesis of A-ring diastereomers of 1 alpha,25-dihydroxyvitamin D2 and 3-methyl-1,25-dihydroxyvitamin D3.

Konno K, Maki S, Fujishima T, Liu Z, Miura D, Chokki M, Takayama H. Konno K, et al. Bioorg Med Chem Lett. 1998 Jan 20;8(2):151-6. doi: 10.1016/s0960-894x(97)10204-9. Bioorg Med Chem Lett. 1998. PMID: 9871644

9

Synthesis and biological activity of 2-methyl-20-epi analogues of 1 alpha,25-dihydroxyvitamin D3.

Fujishima T, Liu Z, Miura D, Chokki M, Ishizuka S, Konno K, Takayama H. Fujishima T, et al. Bioorg Med Chem Lett. 1998 Aug 18;8(16):2145-8. doi: 10.1016/s0960-894x(98)00363-1. Bioorg Med Chem Lett. 1998. PMID: 9873502

10

Synthesis, biological evaluation, and conformational analysis of A-ring diastereomers of 2-methyl-1,25-dihydroxyvitamin D(3) and their 20-epimers: unique activity profiles depending on the stereochemistry of the A-ring and at C-20.

Konno K, Fujishima T, Maki S, Liu Z, Miura D, Chokki M, Ishizuka S, Yamaguchi K, Kan Y, Kurihara M, Miyata N, Smith C, DeLuca HF, Takayama H. Konno K, et al. J Med Chem. 2000 Nov 2;43(22):4247-65. doi: 10.1021/jm000261j. J Med Chem. 2000. PMID: 11063621

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