Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Jamia Hamdard (Hamdard University), Hamdard Nagar, New Delhi, India.
J Enzyme Inhib Med Chem. 2012 Oct;27(5):658-65. doi: 10.3109/14756366.2011.606543. Epub 2011 Sep 8.
Several 2,5-disubstituted-1,3,4-oxadiazoles (4a-f) and 3,6-disubstituted-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles (7a-f) were synthesized and characterized by elemental analyses and spectral data. These compounds were screened for their anti-inflammatory, analgesic, ulcerogenic and lipid peroxidation activities. Compound 7c showed excellent anti-inflammatory and remarkable analgesic activity with reduced ulcerogenic and lipid peroxidation activity when compared with ibuprofen.
几种 2,5-二取代-1,3,4-噁二唑(4a-f)和 3,6-二取代-1,2,4-三唑并[3,4-b]-1,3,4-噻二唑(7a-f)被合成并通过元素分析和光谱数据进行了表征。这些化合物被筛选其抗炎、镇痛、致溃疡和脂质过氧化活性。与布洛芬相比,化合物 7c 表现出优异的抗炎和显著的镇痛活性,同时降低了致溃疡和脂质过氧化活性。