首页> 外文OA文献 >New e:b-Friedo-Hopane Type Triterpenoids from Euphorbia peplus with Simiarendiol Possessing Significant Cytostatic Activity against HeLa Cells by Induction of Apoptosis and S/G2 Cell Cycle Arrest
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New e:b-Friedo-Hopane Type Triterpenoids from Euphorbia peplus with Simiarendiol Possessing Significant Cytostatic Activity against HeLa Cells by Induction of Apoptosis and S/G2 Cell Cycle Arrest

机译:新E:B-Friedo-Hopane类型来自大戟属Peplus的三萜类化合物,Simiarendiol通过诱导细胞凋亡和S / G2细胞循环捕获来对Hela细胞具有显着的细胞抑制活性

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摘要

Seven rare e:b-friedo-hopane-type triterpenoids including four new (1−4) and three known (5−7) ones with 5 being first reported as a natural product, together with five other known triterpenoids (8−12), were isolated from the nonpolar fractions of the ethanolic extract of Euphorbia peplus. Structural assignments for these compounds were based on spectroscopic analyses and quantum chemical computation method. The structural variations for the C-21 isopropyl group, including dehydrogenation (1 and 3) and hydroxylation at C-22 (simiarendiol, 2), were the first cases among e:b-friedo-hopane-type triterpenoids. Simiarendiol (2) bearing a 22-OH showed significant cytostatic activity against HeLa and A549 human tumor cell lines with IC50 values of 3.93 ± 0.10 and 7.90 ± 0.31 μM, respectively. The DAPI staining and flow cytometric analysis revealed that simiarendiol (2) effectively induced cell apoptosis and arrested cell cycle at the S/G2 phases in a dose-dependent manner in HeLa cells.
机译:七个罕见的e:b-弗里非多血液型三萜类化合物,包括四个新(1-4)和三个已知(5-7)型,其中5个,其中5名是一种首先作为天然产物报告,与其他5个其他已知的三萜(8-12)一起报告从大戟属peplus的乙醇提取物的非极性分数中分离出来。这些化合物的结构分配基于光谱分析和量子化学计算方法。 C-21异丙基的结构变化包括脱氢(1和3)和C-22(Simiarendiol,2)的羟基化,是E:B-弗里非酚型三萜类化合物中的第一种情况。 Simiarendiol(2)轴承22-OH分别显示出对Hela和A549人肿瘤细胞系的显着细胞抑制活性,IC50值分别为3.93±0.10和7.90±0.31μm。 DAPI染色和流式细胞术分析表明,Simiarendiol(2)在HeLa细胞中以剂量依赖性方式有效地诱导了S / G2相位的细胞凋亡和阻止细胞周期。

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