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WU Maocheng, LI Xiang, WU Qiuye. Synthesis and antifungal activities of novel triazole derivatives[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 186-190. doi: 10.3969/j.issn.1006-0111.2014.03.006
Citation: WU Maocheng, LI Xiang, WU Qiuye. Synthesis and antifungal activities of novel triazole derivatives[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 186-190. doi: 10.3969/j.issn.1006-0111.2014.03.006

Synthesis and antifungal activities of novel triazole derivatives

doi: 10.3969/j.issn.1006-0111.2014.03.006
  • Received Date: 2014-04-16
  • Rev Recd Date: 2014-04-29
  • Objective To synthesize a new series of triazole compounds with naphthalene benzyl as side chain and evaluate the antifungal activity. Methods Nine title compounds were synthesized and determined by the 1H NMR and MS spectra. According to the method recommended by the national committee for clinical laboratory standards(NCCLS), the RPMI-1640 test medium was used,the antifungal activities of all the compounds were evaluated against eight human pathogenic fungi in vitro. Results The title compounds exhibited potent antifungal activities. Compound 1c showed high activities against 7 funguses except Aspergillus fumigatus with the MIC80 values less than 0.125 μg/ml, which was 16 times higher than that of Voriconazole. Conclusion The title compounds with naphthalene and alkyl substituent showed potent antifungal activities.
  • [1] Zou Y, Yu S, Li R, et al. Synthesis, antifungal activities and molecular docking studies of novel 2-(2,4-difluorophenyl)-2-hydroxy-3-(1H-1,2,4-triazol-1-yl)propyl dithiocarbamates[J].Eur J Med Chem, 2014,74(3):366-374.
    [2] Tang H, Zheng CH, Ren XH, et al. Synthesis and biological evaluation of novel triazole derivatives as antifungal agents[J].Chin Chem Lett, 2013,24(3): 219-222.
    [3] Wang S, Jin G, Wang W, et al.synthesis and structure-activity relationships of new triazole derivatives containing N-substituted phenoxypropylamino side chains[J]. Eur J Med Chem, 2012,53(4): 292-299.
    [4] Zou Y, Zhao Q, Liao J, et al. New triazole derivatives as antifungal agents: synthesis via click reaction, in vitro evaluation and molecular docking studies[J].Bioorg Med Chem Lett, 2012,22(8):2959-2962.
    [5] Jiang Y, Zhang J, Cao Y,et al. Synthesis, in vitro evaluation and molecular docking studies of new triazole derivatives as antifungal agents[J]. Bioorg Med Chem Lett,2011, 21(15): 4471-4475.
    [6] Chai X, Zhang J, Cao Y,et al. Design, synthesis and molecular docking studies of novel triazole as antifungal agent[J]. Eur J Med Chem, 2011, 46(7): 3167-3176.
    [7] National Committee for Clinical Laboratory Standards.Reference method for broth dilution antifungal susceptibility testing of yeasts approved standard[S]. Document M27-A2, Wayne, PA, 2002.
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Synthesis and antifungal activities of novel triazole derivatives

doi: 10.3969/j.issn.1006-0111.2014.03.006

Abstract: Objective To synthesize a new series of triazole compounds with naphthalene benzyl as side chain and evaluate the antifungal activity. Methods Nine title compounds were synthesized and determined by the 1H NMR and MS spectra. According to the method recommended by the national committee for clinical laboratory standards(NCCLS), the RPMI-1640 test medium was used,the antifungal activities of all the compounds were evaluated against eight human pathogenic fungi in vitro. Results The title compounds exhibited potent antifungal activities. Compound 1c showed high activities against 7 funguses except Aspergillus fumigatus with the MIC80 values less than 0.125 μg/ml, which was 16 times higher than that of Voriconazole. Conclusion The title compounds with naphthalene and alkyl substituent showed potent antifungal activities.

WU Maocheng, LI Xiang, WU Qiuye. Synthesis and antifungal activities of novel triazole derivatives[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 186-190. doi: 10.3969/j.issn.1006-0111.2014.03.006
Citation: WU Maocheng, LI Xiang, WU Qiuye. Synthesis and antifungal activities of novel triazole derivatives[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 186-190. doi: 10.3969/j.issn.1006-0111.2014.03.006
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