Discovery of benzylthio analogs of fluconazole as potent antifungal agents

被引:22
|
作者
Motahari, Kamran [1 ]
Badali, Hamid [2 ]
Hashemi, Seyedeh Mahdieh [3 ,4 ]
Fakhim, Hamed [5 ]
Mirzaei, Hassan [6 ]
Vaezi, Afsane [7 ]
Shokrzadeh, Mohammad [8 ]
Emami, Saeed [3 ,4 ]
机构
[1] Mazandaran Univ Med Sci, Student Res Comm, Fac Pharm, Sari, Iran
[2] Mazandaran Univ Med Sci, Dept Med Mycol & Parasitol, Fac Med, IFRC, Sari, Iran
[3] Mazandaran Univ Med Sci, Fac Pharm, Dept Med Chem, Sari, Iran
[4] Mazandaran Univ Med Sci, Fac Pharm, Pharmaceut Sci Res Ctr, Sari, Iran
[5] Urmia Univ Med Sci, Dept Med Parasitol & Mycol, Cellular & Mol Res Ctr, Orumiyeh, Iran
[6] Mazandaran Univ Med Sci, Pharmaceut Sci Res Ctr, Student Res Comm, Fac Pharm, Sari, Iran
[7] Mazandaran Univ Med Sci, Sch Med, Student Res Comm, Sari, Iran
[8] Mazandaran Univ Med Sci, Fac Pharm, Dept Toxicol & Pharmacol, Sari, Iran
关键词
antifungal activity; azole antifungals; fluconazole; lanosterol; 14; alpha-demethylase; triazole; CANDIDA-ALBICANS; DERIVATIVES; DESIGN; SCAFFOLD;
D O I
10.4155/fmc-2017-0295
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Aim: A new series of triazole alcohol antifungals 8a-j were designed by introducing benzylthio functionality on one triazole ring of fluconazole. Results: The antifungal activity evaluation of target compounds against 16 Candida isolates indicated that all compounds with MIC values of 0.063-1 mu g/ml had better profile of activity in respect to fluconazole (MICs = 0.5-4 mu g/ml) against fluconazole-susceptible isolates. In particular, the representative compounds 8b and 8e were also active against fluconazole-resistant isolates of Candida albicans and Candida parapsilosis (MICs = 0.063-16 mu g/ml). Cytotoxicity assay against Hep-G2 and NIH-3T3 cell lines revealed that these compounds can display potent antifungal activity at noncytotoxic concentrations. Conclusion: The prototype compound 8b could be considered as a new lead for design and development of potent antifungal agents. [GRAPHICS] .
引用
收藏
页码:987 / 1002
页数:16
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