Zhang W - Search Results

1

From antidiabetic to antifungal: discovery of highly potent triazole-thiazolidinedione hybrids as novel antifungal agents.

Wu S, Zhang Y, He X, Che X, Wang S, Liu Y, Jiang Y, Liu N, Dong G, Yao J, Miao Z, Wang Y, Zhang W, Sheng C. Wu S, et al. Among authors: zhang w, zhang y. ChemMedChem. 2014 Dec;9(12):2639-46. doi: 10.1002/cmdc.201402320. Epub 2014 Sep 5. ChemMedChem. 2014. PMID: 25196996

2

[Synthesis and antifungal activities of 1-(2-[(substituted-phenyl) methyl]thio)-2-(2,4-difluorophenyl)ethyl-1H-1,2,4-triazoles].

Zhou YJ, Zhang WN, Lu JG, Li K, Zhu J. Zhou YJ, et al. Among authors: zhang wn. Yao Xue Xue Bao. 1997 Dec;32(12):902-7. Yao Xue Xue Bao. 1997. PMID: 11596186 Chinese.

3

[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: zhang wn. Yao Xue Xue Bao. 1997 Aug;32(8):593-9. Yao Xue Xue Bao. 1997. PMID: 11596308 Chinese.

4

Structure-based de novo design, synthesis, and biological evaluation of non-azole inhibitors specific for lanosterol 14alpha-demethylase of fungi.

Ji H, Zhang W, Zhang M, Kudo M, Aoyama Y, Yoshida Y, Sheng C, Song Y, Yang S, Zhou Y, Lü J, Zhu J. Ji H, et al. Among authors: zhang m, zhang w. J Med Chem. 2003 Feb 13;46(4):474-85. doi: 10.1021/jm020362c. J Med Chem. 2003. PMID: 12570370

5

[Synthesis, preliminary antigastrelcosis activity and the protective effect on acute liver injury of zinc chlorin E4].

Yao JZ, Liu JF, Zhang WN, Zhou YJ, Zhu J, Lu JG, Wang XY. Yao JZ, et al. Among authors: zhang wn. Yao Xue Xue Bao. 2001 Mar;36(3):188-91. Yao Xue Xue Bao. 2001. PMID: 12580085 Chinese.

6

[Synthesis and antifungal activity of 1-(1,2,4-triazolyl-1H-1-yl)-2-(2,4-diflurophenyl)-3-(4-substituted benzyl-1-piperazinyl)-2-propanols].

Sheng CQ, Zhang WN, Ji HT, Song YL, Yang S, Zhou YJ, Zhu J, Lü JG. Sheng CQ, et al. Yao Xue Xue Bao. 2003 Sep;38(9):665-70. Yao Xue Xue Bao. 2003. PMID: 14730915 Chinese.

7

[Synthesis and antifungal activity of novel triazole antifungal agents].

Sheng CQ, Zhu J, Zhang WN, Song YL, Zhang M, Ji HT, Yu JX, Yao JZ, Yang S, Miao ZY. Sheng CQ, et al. Yao Xue Xue Bao. 2004 Dec;39(12):984-9. Yao Xue Xue Bao. 2004. PMID: 15813026 Chinese.

8

In vitro antifungal activity of ZJ-522, a new triazole restructured from fluconazole and butenafine, against clinically important fungi in comparison with fluconazole and butenafine.

Gao PH, Cao YB, Xu Z, Zhang JD, Zhang WN, Wang Y, Gu J, Cao YY, Li RY, Jia XM, Jiang YY. Gao PH, et al. Biol Pharm Bull. 2005 Aug;28(8):1414-7. doi: 10.1248/bpb.28.1414. Biol Pharm Bull. 2005. PMID: 16079485 Free article.

9

Evolutionary trace analysis of eukaryotic DNA topoisomerase I superfamily: identification of novel antitumor drug binding site.

Song Y, Qi Y, Zhang W, Sheng C, Zhang M, Yao J, Yu J, Miao Z, Zhou Y, Zhu J, Lü J. Song Y, et al. Among authors: zhang m, zhang w. Sci China C Life Sci. 2005 Aug;48(4):375-84. doi: 10.1360/062004-20. Sci China C Life Sci. 2005. PMID: 16248431

10

[N-myristoyltransferase: a novel antifungal target].

Zhu J, Sheng CQ, Zhang WN. Zhu J, et al. Yao Xue Xue Bao. 2005 Sep;40(9):775-81. Yao Xue Xue Bao. 2005. PMID: 16342675 Review. Chinese. No abstract available.

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