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首页> 外文期刊>Journal of Medicinal Chemistry >Discovery and Biological Evaluation of the Novel Naturally Occurring Diterpene Pepluanone as Antiinflammatory Agent
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Discovery and Biological Evaluation of the Novel Naturally Occurring Diterpene Pepluanone as Antiinflammatory Agent

机译:新型天然存在的二萜哌啶酮作为抗炎剂的发现及生物学评价

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摘要

From the whole plant of Euphorbia peplus L.,a new diterpene based on a rare pepluane skeleton,named pepluanone(1),was isolated together with a known pepluane diterpene(2).The stereostructure of pepluanone was determined on the basis of an extensive NMR study,MS data,and chemical reaction.The ability of these compounds to act as antiinflammatory agents has been evaluated for the first time by in vivo tests on carrageenin-induced rat paw edema,an experimental model of acute inflammation.Comparison of the bioactivity of pepluanone and compound 2 in terms of chemical structure,evidenced the high efficiency of pepluanone and the absence of appreciable activity for compound 2,thus giving a first insight into the structure-activity relationship.Further in vitro experiments performed on pepluanone let us hypothesize that its activity could be explained in reducing the production of nitric oxide,prostaglandin E_2,and TNF-alpha by inhibiting the expression of inducible nitric oxide synthase,cyclooxygenase-2,and TNF-alpha mRNA through the down-regulation of NF-kappaB binding activity.
机译:从大戟peplus L.的整个植物中,分离出一种新的基于稀有七环烷骨架的二萜,命名为pepluanone(1)和已知的pepluane diterpene(2)。在广泛的基础上确定了pepluanone的立体结构。 NMR研究,质谱数据和化学反应。首次通过角叉菜胶诱导的大鼠爪水肿的体内试验首次评估了这些化合物作为抗炎药的能力。 pepluanone和化合物2的化学结构方面的数据,证明了pepluanone的高效性和化合物2缺乏明显的活性,因此首次了解了结构活性关系。对pepluanone进行的进一步体外实验让我们假设其活性可以通过抑制诱导型一氧化氮合酶,环的表达来减少一氧化氮,前列腺素E_2和TNF-α的产生。通过下调NF-kappaB结合活性来确定氧合酶2和TNF-αmRNA的表达。

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