首页> 外文期刊>Journal of Medicinal Chemistry >Quantitative Structure-Activity Relationship of Sesquiterpene Lactones as Inhibitors of the Transcription Factor NF-kappaB.
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Quantitative Structure-Activity Relationship of Sesquiterpene Lactones as Inhibitors of the Transcription Factor NF-kappaB.

机译:倍半萜内酯作为转录因子NF-κB抑制剂的定量构效关系。

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摘要

Sesquiterpene lactones (SLs) are the active compounds of a variety of tradionally used medicinal plants from the Asteraceae family. They are known to possess a considerable antiinflammatory activity in different inflammation models. They inhibit the transcription factor NF-kappaB probably by alkylating cysteine38 in the DNA binding domain of the p65 subunit. Here we investigate a set of 103 different sesquiterpene lactones representing 6 structural groups (44 germacranolides, 16 heliangolides, 22 guaianolides, 9 pseudoguaianolides, 2 hypocretenolides, 10 eudesmanolides) for their NF-kappaB inhibiting properties and the resulting IC(100)-values were submitted to a QSAR study. Properties important for the inhibition potency are discussed for the whole data set and for subsets of the different structural classes.
机译:倍半萜内酯(SLs)是菊科(Asteraceae)的许多传统使用的药用植物的活性化合物。已知它们在不同的炎症模型中具有相当大的抗炎活性。它们可能通过使p65亚基的DNA结合域中的半胱氨酸38烷基化来抑制转录因子NF-κB。在这里,我们研究了一组103个不同的倍半萜烯内酯,它们分别代表6个结构组(44个germ草内酯,16个七聚内酯,22个瓜香内酯,9个拟愈创木酚内酯,2个降ides烯内酯,10个正十二烯内酯),它们具有NF-κB抑制特性,其IC(100)值为提交给QSAR研究。对于整个数据集和不同结构类别的子集,讨论了对抑制效能重要的属性。

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