Kaji-ichigoside F1

上海金畔生物科技有限公司提供天然产物萜类及其苷类Terpenoids and Glycosides。

Kaji-ichigoside F1  纯度: ≥98.0%

Kaji-ichigoside F1 是从S. cuneata中分离得到的一种具有溶血性和体外抗病毒活性的化合物。

Kaji-ichigoside F1

Kaji-ichigoside F1 Chemical Structure

CAS No. : 95298-47-8

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生物活性

Kaji-ichigoside F1 is isolated from S. cuneata with hemolytic and in vitro antiviral activity.[1]

分子量

650.84

Formula

C36H58O10

CAS 号

95298-47-8

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

参考文献
  • [1]. Jun Chang, et al.Phenolic glycosides and ionone glycoside from the stem of Sargentodoxa cuneata,Phytochemistry,Phytochemistry. 2005 Dec;66(23):2752-8.

Niga-ichigoside F1(Synonyms: 苦莓苷F1)

天然产物 糖类和糖苷 Saccharides and Glycosides

Niga-ichigoside F1;(Synonyms: 苦莓苷F1)

Niga-ichigoside F1 是一种具有口服活性熊果三萜,具有抗高血脂和抗氧化活性。Niga-ichigoside F1 可以预防高脂肪饮食 (HFD) 诱导的肝脂肪变性。

Niga-ichigoside F1(Synonyms: 苦莓苷F1)

Niga-ichigoside F1 Chemical Structure

CAS No. : 95262-48-9

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5 mg ¥5200 In-stock
10 mg ¥8400 In-stock
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100 mg ; 询价 ;

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Niga-ichigoside F1 相关产品

bull;相关化合物库:

  • Natural Product Library Plus
  • Bioactive Compound Library Plus
  • Natural Product Library
  • Glycoside Compound Library
  • Anti-Cardiovascular Disease Compound Library
  • Terpenoids Library
  • Orally Active Compound Library
  • Traditional Chinese Medicine Monomer Library

生物活性

Niga-ichigoside F1, an orally active ursane triterpenoid, has antihyperlipidemic and antioxidant activities. Niga-ichigoside F1 can prevent high-fat diet (HFD)-induced hepatic steatosis[1].

体外研究
(In Vitro)

Niga-ichigoside F1 (2.5, 5, 10, 20 μM; for 24 hours) inhibits lipid accumu-lation in free fatty acid (FFA)-treated HepG2 cells in a dose-dependent manner. Niga-ichigoside F1 has no effects on cell viability[1].
Both nuclear and cytoplasmic Nrf2 expressions are lowered in Con, Niga-ichigoside F1 (20 μM), FFA (1 mM), and Niga-ichigoside F1 plus FFA treated Nrf2-silenced cells[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Niga-ichigoside F1 (40 mg/kg; oral gavage; for 12 weeks) alleviates hepatic steatosis, possibly by significantly interacting with high-fat diet (HFD) to regulate lipid metabolism genes (including Srebp1c, Acc1, Fasn, Scd1, Cpt1a and Fabp5) in four-week-old male C57BL/6J mice[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

666.84

Formula

C36H58O11

CAS 号

95262-48-9

中文名称

苦莓苷F1

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4deg;C, protect from light

*In solvent : -80deg;C, 6 months; -20deg;C, 1 month (protect from light)

参考文献
  • [1]. Shu-Fang Xia, et al. Niga-ichigoside F1 ameliorates high-fat diet-induced hepatic steatosis in male mice by Nrf2 activation. Food Funct. 2018 Feb 21;9(2):906-916.