Synthesis and Activity Evaluation of New Benzofuran-1,3,4-Oxadiazole Hybrids Against Wood-Degrading Fungi

被引:3
|
作者
Hosseinihashemi, Seyyed Khalil [1 ]
Toolabi, Mahsa [2 ]
Abedinifar, Fahimeh [3 ]
Moghimi, Setareh [3 ]
Jalaligoldeh, Abbas [4 ]
Paknejad, Farzad [5 ]
Arabahmadi, Shahrbanoo [6 ]
Foroumadi, Alireza [2 ,3 ]
机构
[1] Islamic Azad Univ, Karaj Branch, Dept Wood Sci & Paper Technol, Karaj, Iran
[2] Univ Tehran Med Sci, Fac Pharm, Dept Med Chem, Tehran, Iran
[3] Univ Tehran Med Sci, Inst Pharmaceut Sci TIPS, Drug Design & Dev Res Ctr, Tehran, Iran
[4] Islamic Azad Univ, Karaj Branch, Dept Hort Sci, Karaj, Iran
[5] Islamic Azad Univ, Karaj Branch, Dept Agron & Plant Breeding, Karaj, Iran
[6] Univ Mazandaran, Dept Chem, POB 47416-95447, Babol Sar, Iran
关键词
Oxadiazole; Synthesis; Antifungal activity; Wood-degrading fungi; HYDROXYL RADICAL GENERATION; MOLECULAR-WEIGHT SUBSTANCE; PHENOL OXIDASE ACTIVITY; BIOLOGICAL EVALUATION; WHITE-ROT; ANTIMICROBIAL ACTIVITY; SULFONE DERIVATIVES; ANTIFUNGAL ACTIVITY; 1,3,4-OXADIAZOLE; DEGRADATION;
D O I
10.15376/biores.15.1.1085-1097
中图分类号
TB3 [工程材料学]; TS [轻工业、手工业、生活服务业];
学科分类号
0805 ; 080502 ; 0822 ;
摘要
A series of novel benzofuran-1,3,4-oxadiazole hybrids were synthesized and evaluated as antifungal agents. The synthetic pathway was started from salicylaldehyde, which afforded 5-(substituted benzylthio)-1,3,4-oxadiazole derivatives in moderate to good yields. The compounds were investigated for their antifungal potential against white-rot, Trametes versicolor and brown-rot, Poria placenta and Coniophora puteana fungi at different concentrations (500, 1000 ppm). The obtaining results demonstrated that most of the compounds at 500 ppm concentration did not exhibit acceptable antifungal effects but they had better antifungal activity at 1000 ppm concentration. Compounds 5a, 5c, and 5i showed inhibition percentages of 14.6%, 23.0%, and 14.7%, against the growth of P. placenta and C. puteana, respectively. Among the compounds, the 2-(benzofuran-2-yl)-5-((2,6-difluorobenzyl)thio)-1,3,4-oxadiazole (5h) hybrid was the most active one.
引用
收藏
页码:1085 / 1097
页数:13
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