目录:MedChemExpress LLC>>生化试剂>> Isosteviol | MCE
CAS | 27975-19-5 | 纯度 | ≥98.0% |
---|---|---|---|
分子量 | 318.45 | 分子式 | C₂₀H₃₀O₃ |
供货周期 | 现货 | 规格 | 5 mg |
货号 | HY-N0872 | 应用领域 | 医疗卫生,化工,生物产业,制药/生物制药 |
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CAS No. : 27975-19-5
产品活性:Isosteviol ((-)-Isosteviol) is a derivative of Stevioside through acid catalyzed hydrolysis of Stevioside. Isosteviol inhibits DNA polymerase and DNA topoisomerase and has antibacterial, anticancer and anti-tuberculosis effects.
研究领域:Immunology/Inflammation | NF-κB | Metabolic Enzyme/Protease | Cell Cycle/DNA Damage
作用靶点:Reactive Oxygen Species | Topoisomerase
结构分类:萜类 | 二萜
来源:植物 | 其他科
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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