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Items: 15

1.

Design, synthesis, biological evaluation and molecular docking studies of new chalcone derivatives containing diaryl ether moiety as potential anticancer agents and tubulin polymerization inhibitors.

Wang G, Liu W, Gong Z, Huang Y, Li Y, Peng Z.

Bioorg Chem. 2019 Dec 31;95:103565. doi: 10.1016/j.bioorg.2019.103565. [Epub ahead of print]

PMID:
31927336
2.

A Novel Framework with High Diagnostic Sensitivity for Lung Cancer Detection by Electronic Nose.

Lu B, Fu L, Nie B, Peng Z, Liu H.

Sensors (Basel). 2019 Dec 3;19(23). pii: E5333. doi: 10.3390/s19235333.

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Synthesis, biological evaluation and molecular docking studies of aminochalcone derivatives as potential anticancer agents by targeting tubulin colchicine binding site.

Wang G, Peng Z, Zhang J, Qiu J, Xie Z, Gong Z.

Bioorg Chem. 2018 Aug;78:332-340. doi: 10.1016/j.bioorg.2018.03.028. Epub 2018 Apr 3.

PMID:
29627654
7.

Synthesis, biological evaluation, and docking studies of novel 5,6-diaryl-1,2,4-triazine thiazole derivatives as a new class of α-glucosidase inhibitors.

Wang G, Peng Z, Gong Z, Li Y.

Bioorg Chem. 2018 Aug;78:195-200. doi: 10.1016/j.bioorg.2018.03.015. Epub 2018 Mar 21.

PMID:
29587132
8.

Synthesis, In Vitro α-Glucosidase Inhibitory Activity and Molecular Docking Studies of Novel Benzothiazole-Triazole Derivatives.

Gong Z, Peng Y, Qiu J, Cao A, Wang G, Peng Z.

Molecules. 2017 Sep 15;22(9). pii: E1555. doi: 10.3390/molecules22091555.

9.

Synthesis and biological evaluation of novel 2,4,5-triarylimidazole-1,2,3-triazole derivatives via click chemistry as α-glucosidase inhibitors.

Wang G, Peng Z, Wang J, Li J, Li X.

Bioorg Med Chem Lett. 2016 Dec 1;26(23):5719-5723. doi: 10.1016/j.bmcl.2016.10.057. Epub 2016 Oct 21.

PMID:
27810241
10.

Synthesis, in vitro evaluation and molecular docking studies of novel triazine-triazole derivatives as potential α-glucosidase inhibitors.

Wang G, Peng Z, Wang J, Li X, Li J.

Eur J Med Chem. 2017 Jan 5;125:423-429. doi: 10.1016/j.ejmech.2016.09.067. Epub 2016 Sep 21.

PMID:
27689725
11.

Synthesis, in vitro evaluation and molecular docking studies of novel coumarin-isatin derivatives as α-glucosidase inhibitors.

Wang G, Wang J, He D, Li X, Li J, Peng Z.

Chem Biol Drug Des. 2017 Mar;89(3):456-463. doi: 10.1111/cbdd.12867. Epub 2016 Oct 5.

PMID:
27616456
12.

Synthesis, biological evaluation and molecular docking study of N-arylbenzo[d]oxazol-2-amines as potential α-glucosidase inhibitors.

Wang G, Peng Z, Wang J, Li J, Li X.

Bioorg Med Chem. 2016 Nov 1;24(21):5374-5379. doi: 10.1016/j.bmc.2016.08.061. Epub 2016 Aug 30.

PMID:
27614916
13.

Synthesis and biological evaluation of novel 1,2,4-triazine derivatives bearing carbazole moiety as potent α-glucosidase inhibitors.

Wang G, Wang J, He D, Li X, Li J, Peng Z.

Bioorg Med Chem Lett. 2016 Jun 15;26(12):2806-2809. doi: 10.1016/j.bmcl.2016.04.071. Epub 2016 Apr 23.

PMID:
27177827
14.

Design, synthesis and biological evaluation of novel coumarin thiazole derivatives as α-glucosidase inhibitors.

Wang G, He D, Li X, Li J, Peng Z.

Bioorg Chem. 2016 Apr;65:167-74. doi: 10.1016/j.bioorg.2016.03.001. Epub 2016 Mar 2.

PMID:
26964016
15.

[Selection of reference genes for virulence gene expression in Vibrio parahaemolyticus].

Li Q, Peng Z, Chen X, Sun X, Pan Y, Zhao Y.

Wei Sheng Wu Xue Bao. 2013 Mar 4;53(3):306-12. Chinese.

PMID:
23678578

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