Cao Y - Search Results

1

New azoles with potent antifungal activity: design, synthesis and molecular docking.

Che X, Sheng C, Wang W, Cao Y, Xu Y, Ji H, Dong G, Miao Z, Yao J, Zhang W. Che X, et al. Among authors: cao y. Eur J Med Chem. 2009 Oct;44(10):4218-26. doi: 10.1016/j.ejmech.2009.05.018. Epub 2009 May 24. Eur J Med Chem. 2009. PMID: 19539408

2

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. Among authors: cao yb, cao yy. Biol Pharm Bull. 2005 Aug;28(8):1414-7. doi: 10.1248/bpb.28.1414. Biol Pharm Bull. 2005. PMID: 16079485 Free article.

3

Antifungal activities and action mechanisms of compounds from Tribulus terrestris L.

Zhang JD, Xu Z, Cao YB, Chen HS, Yan L, An MM, Gao PH, Wang Y, Jia XM, Jiang YY. Zhang JD, et al. Among authors: cao yb. J Ethnopharmacol. 2006 Jan 3;103(1):76-84. doi: 10.1016/j.jep.2005.07.006. Epub 2005 Oct 5. J Ethnopharmacol. 2006. PMID: 16169173

4

[Cloning and expression of the mutant 14alpha-demethylase containing the alteration of H310D in Candida albicans and the preliminary study on its functions].

Gao P, Cao Y, Xu Z, Liu H, Jiang Y. Gao P, et al. Among authors: cao y. Wei Sheng Wu Xue Bao. 2003 Dec;43(6):712-6. Wei Sheng Wu Xue Bao. 2003. PMID: 16276890 Chinese.

5

In vitro and in vivo antifungal activities of the eight steroid saponins from Tribulus terrestris L. with potent activity against fluconazole-resistant fungal pathogens.

Zhang JD, Cao YB, Xu Z, Sun HH, An MM, Yan L, Chen HS, Gao PH, Wang Y, Jia XM, Jiang YY. Zhang JD, et al. Among authors: cao yb. Biol Pharm Bull. 2005 Dec;28(12):2211-5. doi: 10.1248/bpb.28.2211. Biol Pharm Bull. 2005. PMID: 16327151 Free article.

6

Drug susceptibilities of yeast cells are affected when expressing mutant Candida albicans drug resistance protein.

Gao PH, Cao YB, Jia XM, Cao YY, Quan H, Wang Y, Jiang YY. Gao PH, et al. Among authors: cao yb, cao yy. Int J Antimicrob Agents. 2006 Jul;28(1):69-74. doi: 10.1016/j.ijantimicag.2006.02.016. Epub 2006 Jun 19. Int J Antimicrob Agents. 2006. PMID: 16782311

7

In vitro and in vivo activities of HQQ-3, a new triazole antifungal agent.

Zhao JX, Cao YY, Quan H, Liu CM, He QQ, Wu QY, Gao PH, Cao YB, Liu WX, Jiang YY. Zhao JX, et al. Biol Pharm Bull. 2006 Oct;29(10):2031-4. doi: 10.1248/bpb.29.2031. Biol Pharm Bull. 2006. PMID: 17015946 Free article.

8

Synthesis and evaluation of novel 1-(1H-1,2,4-triazol-1-yl)-2-(2,4-difluorophenyl)-3-[(4-substitutedphenyl)-piperazin-1-yl]-propan-2-ols as antifungal agents.

Sun QY, Zhang WN, Xu JM, Cao YB, Wu QY, Zhang DZ, Liu CM, Yu SC, Jiang YY. Sun QY, et al. Eur J Med Chem. 2007 Aug;42(8):1151-7. doi: 10.1016/j.ejmech.2006.11.003. Epub 2006 Nov 24. Eur J Med Chem. 2007. PMID: 17184885

9

Fcr1p inhibits development of fluconazole resistance in Candida albicans by abolishing CDR1 induction.

Shen H, An MM, Wang de J, Xu Z, Zhang JD, Gao PH, Cao YY, Cao YB, Jiang YY. Shen H, et al. Biol Pharm Bull. 2007 Jan;30(1):68-73. doi: 10.1248/bpb.30.68. Biol Pharm Bull. 2007. PMID: 17202662 Free article.

10

Synthesis of novel triazole derivatives as inhibitors of cytochrome P450 14alpha-demethylase (CYP51).

Sun QY, Xu JM, Cao YB, Zhang WN, Wu QY, Zhang DZ, Zhang J, Zhao HQ, Jiang YY. Sun QY, et al. Eur J Med Chem. 2007 Sep;42(9):1226-33. doi: 10.1016/j.ejmech.2007.01.006. Epub 2007 Jan 24. Eur J Med Chem. 2007. PMID: 17335940

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