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目录:MedChemExpress LLC>>生化试剂>> Isosteviol | MCE

Isosteviol | MCE
  • Isosteviol | MCE
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参考价 1000
具体成交价以合同协议为准
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更新时间:2023-06-08 11:30:39浏览次数:153评价

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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
Isosteviol | MCEIsosteviol ((-)-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<sup>[1]</sup><sup>[2]</sup><sup>[3]</sup><sup>[4]</sup>.

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Isosteviol

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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