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首页> 外文期刊>Medicinal chemistry research: an international journal for rapid communications on design and mechanisms of action of biologically active agents >Synthesis and anti-inflammatory activity evaluation of novel 3-alkyl-6-(4H-1,2,4-triazol-4-yl)-3,4-dihydro-2H-benzo[e][1,3]oxazine derivatives
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Synthesis and anti-inflammatory activity evaluation of novel 3-alkyl-6-(4H-1,2,4-triazol-4-yl)-3,4-dihydro-2H-benzo[e][1,3]oxazine derivatives

机译:新型3-烷基-6-(4H-1,2,4-三唑-4-基)-3,4-二氢-2H-苯并[e] [1,3]恶嗪衍生物的合成及抗炎活性评估

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摘要

To discover new compounds with anti-inflammatory activity, a series of novel 3-alkyl-6-(4H-1,2,4-triazol-4-yl)-3,4-dihydro-2H-benzo[e][1,3]oxazine derivatives were synthesized and their structures were confirmed by spectroscopic techniques. In vivo anti-inflammatory activity of the synthesized compounds was determined using the xylene-induced mouse ear edema model. 3-Heptyl-6-(4H-1,2,4-triazol-4-yl)-3,4-dihydro-2H-benzo[e] [1,3]oxazine and 3-p-tolyl-6-(4H-1,2,4-triazol-4-yl)-3,4-dihydro-2H-benzo[e][1,3]oxazine demonstrated higher anti-inflammatory activity (74.04 % and 64.99 %, respectively) at 0.5 h after intraperitoneal administration than the reference drug ibuprofen (62.65 %). Further, the time of peak effect after oral administration was 4 h for both compounds. Our results identify new compounds with anti-inflammatory activity in vivo that may have improved safety/side effect profiles relative to the currently approved nonsteroidal anti-inflammatory drugs.
机译:为了发现具有抗炎活性的新化合物,一系列新的3-烷基-6-(4H-1,2,4-三唑-4-基)-3,4-二氢-2H-苯并[e] [1]合成了3,3]恶嗪衍生物,并通过光谱技术确定了其结构。使用二甲苯诱导的小鼠耳朵水肿模型确定了合成化合物的体内抗炎活性。 3-庚基-6-(4H-1,2,4-三唑-4-基)-3,4-二氢-2H-苯并[e] [1,3]恶嗪和3-对甲苯基-6-( 4H-1,2,4-三唑-4-基)-3,4-二氢-2H-苯并[e] [1,3]恶嗪在0.5下显示较高的抗炎活性(分别为74.04%和64.99%)腹膜内给药后h比参考药物布洛芬(62.65%)。另外,两种化合物口服给药后的峰值作用时间均为4小时。我们的结果确定了相对于当前批准的非甾体类抗炎药,在体内具有抗炎活性的新化合物,其具有改善的安全性/副作用。

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