Sheng C - Search Results

1

Design, synthesis and structure-activity relationships of new triazole derivatives containing N-substituted phenoxypropylamino side chains.

Wang S, Jin G, Wang W, Zhu L, Zhang Y, Dong G, Liu Y, Zhuang C, Miao Z, Yao J, Zhang W, Sheng C. Wang S, et al. Among authors: sheng c. Eur J Med Chem. 2012 Jul;53:292-9. doi: 10.1016/j.ejmech.2012.04.013. Epub 2012 Apr 19. Eur J Med Chem. 2012. PMID: 22560626

2

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: sheng c. J Med Chem. 2003 Feb 13;46(4):474-85. doi: 10.1021/jm020362c. J Med Chem. 2003. PMID: 12570370

3

[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.

4

[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.

5

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: sheng c. Sci China C Life Sci. 2005 Aug;48(4):375-84. doi: 10.1360/062004-20. Sci China C Life Sci. 2005. PMID: 16248431

6

[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.

7

Structure-based optimization of azole antifungal agents by CoMFA, CoMSIA, and molecular docking.

Sheng C, Zhang W, Ji H, Zhang M, Song Y, Xu H, Zhu J, Miao Z, Jiang Q, Yao J, Zhou Y, Zhu J, Lü J. Sheng C, et al. J Med Chem. 2006 Apr 20;49(8):2512-25. doi: 10.1021/jm051211n. J Med Chem. 2006. PMID: 16610794

8

3D-QSAR and molecular docking studies on benzothiazole derivatives as Candida albicans N-myristoyltransferase inhibitors.

Sheng C, Zhu J, Zhang W, Zhang M, Ji H, Song Y, Xu H, Yao J, Miao Z, Zhou Y, Zhu J, Lü J. Sheng C, et al. Eur J Med Chem. 2007 Apr;42(4):477-86. doi: 10.1016/j.ejmech.2006.11.001. Epub 2006 Nov 18. Eur J Med Chem. 2007. PMID: 17349719

9

[Evolutionary trace analysis of N-myristoyltransferase family].

Sheng CQ, Zhu J, Zhang WN, Xu H, Miao ZY, Yao JZ, Zhang M. Sheng CQ, et al. Yao Xue Xue Bao. 2007 Feb;42(2):157-65. Yao Xue Xue Bao. 2007. PMID: 17518043 Chinese.

10

Identification of Y118 amino acid residue in Candida albicans sterol 14alpha-demethylase associated with the enzyme activity and selective antifungal activity of azole analogues.

Chen SH, Sheng CQ, Xu XH, Jiang YY, Zhang WN, He C. Chen SH, et al. Among authors: sheng cq. Biol Pharm Bull. 2007 Jul;30(7):1246-53. doi: 10.1248/bpb.30.1246. Biol Pharm Bull. 2007. PMID: 17603162 Free article.

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