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Inhibitory Effects of Momordin I Derivatives on the Formation of Fos-Jun-AP-1 DNA Complex

机译:Momordin I衍生物对Fos-Jun-AP-1 DNA复合物形成的抑制作用

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摘要

In our previous studies,we have observed that curcumin and momordin I isolated from Ampelopsis radix inhibit the formation of Fos-Jun-activation protein-1(AP-1)DNA complex.We have screened more effective compounds which have a 5-membered ring framework like momordin I and have modified disaccharide or carboxylic acid portions in momordin I.We synthesized momordin I derivatives according to the published method with slight modification.Synthetic momordin I derivatives showed remarkable inhibitory activities on Fos-Jun-AP-1 DNA complex formation results in in vitro assays.The IC_(50)values of momordin I derivatives were about 4.0 muM in an electrophoretic mobility shift assay(EMSA).This value is about 125 times higher than that of curcumin and about 12 times higher than that for curcumin derivative Cl,and moreover about 30 times higher than that for momordin I.We found momordin I derivatives(a)and(b)are the strongest inhibitory compound for Fos-Jun-AP-1 DNA complex formation.
机译:在我们以前的研究中,我们观察到从安眠草中分离得到的姜黄素和苦瓜素I抑制了Fos-Jun活化蛋白-1(AP-1)DNA复合物的形成。我们筛选了更有效的具有5元环的化合物分子框架如momordin I,并在momordin I中修饰了二糖或羧酸部分。我们根据公开的方法合成了momordin I衍生物,并对其进行了轻微修饰。合成的momordin I衍生物对Fos-Jun-AP-1 DNA复合物的形成结果显示出显着的抑制活性。在体外实验中,在电泳迁移率迁移分析(EMSA)中,momordin I衍生物的IC_(50)值约为4.0μM,比姜黄素高约125倍,比姜黄素衍生物高约12倍Cl,而且比momordin I高约30倍。我们发现momordin I衍生物(a)和(b)是对Fos-Jun-AP-1 DNA复合物形成最强的抑制化合物。

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