Design and One-Pot and Microwave-Assisted Synthesis of 2-Amino/5-Aryl-1,3,4-oxadiazoles Bearing a Benzimidazole Moiety as Antioxidants
ARCHIV DER PHARMAZIE, cilt.345, sa.7, ss.549-556, 2012 (SCI-Expanded, Scopus)
- Yayın Türü: Makale / Tam Makale
- Cilt numarası: 345 Sayı: 7
- Basım Tarihi: 2012
- Doi Numarası: 10.1002/ardp.201100440
- Dergi Adı: ARCHIV DER PHARMAZIE
- Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Index Chemicus (IC)
- Sayfa Sayıları: ss.549-556
- Anahtar Kelimeler: Antioxidant activity, Benzimidazoles, Oxadiazoles, X-ray, LIPID PEROXIDE FORMATION, 1,3,4-OXADIAZOLE DERIVATIVES, FREE-RADICALS, ANTIBACTERIAL, ANTIFUNGAL, ACID
- Ondokuz Mayıs Üniversitesi Adresli: Evet
Özet
In this study, two new series of 2-amino-1,3,4-oxadiazoles and 5-aryl-1,3,4-oxadiazoles carrying a benzimidazole moiety were synthesized. The antioxidant properties of these compounds were investigated in vitro by the determination of the microsomal NADPH-dependent inhibition of lipid peroxidation levels (LP), the microsomal ethoxyresorufin O-deethylase activity (EROD), and DPPH radical scavenger effects. Among the tested compounds, 2-[(2-(4-chlorophenyl)-1H-benzo[d]imidazole-1-yl)methyl]-5-(4-fluorophenyl)-1,3,4-oxadiazole (9) was found to be the most active compound in all three in vitro systems.