A novel series of thiazolyl-pyrazoline derivatives: Synthesis and evaluation of antifungal activity, cytotoxicity and genotoxicity

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Altıntop M. D., Özdemir A., Turan-Zitouni G., Ilgın S., Atli Ö., Demirel R., ...Daha Fazla

European Journal of Medicinal Chemistry, cilt.92, ss.342-352, 2015 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 92
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1016/j.ejmech.2014.12.055
  • Dergi Adı: European Journal of Medicinal Chemistry
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Index Chemicus (IC)
  • Sayfa Sayıları: ss.342-352
  • Anahtar Kelimeler: Thiazole, Pyrazoline, Antifungal activity, Cytotoxicity, Genotoxicity, POTENTIAL ANTICANCER AGENTS, BIOLOGICAL EVALUATION, ANTITUMOR-ACTIVITY, DRUG-RESISTANCE, IN-VITRO, HEPATOCELLULAR-CARCINOMA, ANTIMICROBIAL ACTIVITY, HYDRAZONE DERIVATIVES, MOLECULAR DOCKING, INHIBITORS
  • Anadolu Üniversitesi Adresli: Evet

Özet

In the current work, new thiazolyl-pyrazoline derivatives (1-22) were synthesized and evaluated for their antifungal effects against pathogenic yeasts and molds using a broth microdilution assay. Ames assay was carried out to determine the genotoxicity of the most effective antifungal derivatives. The cytotoxicity of the compounds (1-22) was also investigated against A549 human lung adenocarcinoma and NIH/3T3 mouse embryonic fibroblast cells. Among these derivatives, 2-[5-(4-fluorophenyl)-3-(5-methylthiophen-2-yl)-4,5-dihydro-1H-pyrazol-1-yl]-4-(4-methylsulfonylphenyl)thiazole (18) can be identified as the most promising anticandidal derivative due to its notable inhibitory effect on Candida zeylanoides with a MIC value of 250 μg/mL when compared with ketoconazole (MIC = 250 μg/mL), low cytotoxicity against NIH/3T3 cells and non-mutagenic effect. On the other hand, 2-[5-(4-fluorophenyl)-3-(5-chlorothiophen-2-yl)-4,5-dihydro-1H-pyrazol-1-yl]-4-(4-bromophenyl)thiazole (4) can be considered as the most promising anticancer agent against A549 cancer cells owing to its notable inhibitory effect on A549 cells with an IC50 value of 62.5 μg/mL when compared with cisplatin (IC50 = 45.88 mg/mL) and low cytotoxicity against NIH/3T3 cells.