型号:
产品价格:电议      采购度:1613      原产地:美洲
发布时间:2021/7/21 14:07:25 所属地区:上海 上海市
简要描述:
Isosteviol ((-)-Isosteviol) 是一种甜菊糖苷衍生物,是甜菊糖苷通过酸催化水解产生的。Isosteviol 抑制 DNA 聚合酶和 DNA 拓扑异构酶,并具有抗菌,抗癌和抗结核作用。
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CAS No. : 27975-19-5
MCE 站:Isosteviol
产品活性:Isosteviol ((-)-Isosteviol) 是一种甜菊糖苷衍生物,是甜菊糖苷通过酸催化水解产生的。Isosteviol 抑制 DNA 聚合酶和 DNA 拓扑异构酶,并具有抗菌,抗癌和抗结核作用。
研究领域:Immunology/Inflammation | NF-κB | Metabolic Enzyme/Protease | Cell Cycle/DNA Damage
作用靶点:Reactive Oxygen Species | Topoisomerase
In Vitro: Isosteviol ((-)-Isosteviol) dose-dependently relaxed the vasopressin (10-8 M)-induced vasoconstriction in isolated aortic rings with or without endothelium. However, in the presence of potassium chloride (3×10-2 M), the vasodilator effect of isosteviol on arterial strips disappeared. Only the inhibitors specific for the ATP-sensitive potassium (KATP) channel or small conductance calcium-activated potassium (SKCa) channel inhibited the vasodilator effect of isosteviol in isolated aortic rings contracted with 10-8 M vasopressin.
The attenuation by isosteviol of the vasopressin- and phenylephrine-induced increase in [Ca2+]i was inhibited by glibenclamide, apamin and 4-aminopyridine but not by charybdotoxin. Furthermore, the inhibitory action of isosteviol on [Ca 2+]i was blocked when A7r5 cells co-treated with glibenclamide and apamin in conjunction with 4-aminopyridine were present.
Isosteviol (1-100 micromol/l) inhibits angiotensin-II-induced DNA synthesis and endothelin-1 secretion. Measurements of 2'7'-dichlorofluorescin diacetate, a redox-sensitive fluorescent dye, showed an isosteviol-mediated inhibition of intracellular reactive oxygen species generated by the effects of angiotensin II.
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更新时间:2024/1/2 10:14:03
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