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  3. Notoginsenoside Fe

Notoginsenoside Fe  (Synonyms: Notoginseng triterpenes; Ginsenoside Mb)

Cat. No.: HY-N0046 Purity: 99.99%
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Notoginsenoside Fe (Notoginseng triterpenes; Ginsenoside Mb) is a saponin with anti-obesity and anti-neuroblastoma activities. Notoginsenoside Fe can be isolated from leaves of Panax notoginseng. Notoginsenoside Fe specifically activates paraventricular nucleus neurons in the hypothalamus, effectively reducing body weight, improving fasting blood glucose and protecting liver function by decreasing food intake, increasing resting metabolic rate and enhancing energy expenditure. Notoginsenoside Fe also inhibits the c-Src signaling pathway, blocks the proliferation and viability of human neuroblastoma cells, while improving mitochondrial dysfunction and alleviating apoptosis. Notoginsenoside Fe can be used in studies related to diet-induced obesity and neuroblastoma.

For research use only. We do not sell to patients.

Notoginsenoside Fe

Notoginsenoside Fe Chemical Structure

CAS No. : 88105-29-7

Size Price Stock Quantity
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in Water
ready for reconstitution
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10 mM * 1 mL in Water In-stock
Solid
5 mg In-stock
10 mg In-stock
25 mg In-stock
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Description

Notoginsenoside Fe (Notoginseng triterpenes; Ginsenoside Mb) is a saponin with anti-obesity and anti-neuroblastoma activities. Notoginsenoside Fe can be isolated from leaves of Panax notoginseng. Notoginsenoside Fe specifically activates paraventricular nucleus neurons in the hypothalamus, effectively reducing body weight, improving fasting blood glucose and protecting liver function by decreasing food intake, increasing resting metabolic rate and enhancing energy expenditure. Notoginsenoside Fe also inhibits the c-Src signaling pathway, blocks the proliferation and viability of human neuroblastoma cells, while improving mitochondrial dysfunction and alleviating apoptosis. Notoginsenoside Fe can be used in studies related to diet-induced obesity and neuroblastoma[1][2][3].

In Vitro

Notoginsenoside Fe (50 μM; 24 h) significantly reduces cell viability of human neuroblastoma SH-SY5Y cells, with a weaker inhibitory effect than notoginsenoside Ft1 (HY-N0910)[3].

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

Cell Viability Assay[3]

Cell Line: human neuroblastoma SH-SY5Y cells
Concentration: 50 μM
Incubation Time: 24 h
Result: Significantly inhibited the viability of SH-SY5Y cells, though its inhibitory effect was weaker than that of notoginsenoside Ft1.
In Vivo

Notoginsenoside Fe (10 mg/kg; i.p.; daily; 14 days) reduces diet-induced obesity in male C57BL/6 mice by decreasing body weight by 12%, reducing food intake, improving glucose tolerance, ameliorating hepatic steatosis, reducing fat mass, increasing energy expenditure, and inhibiting lipogenesis gene expression[1].
Notoginsenoside Fe (5 mM in 2 μl per mouse; i.c.v.; single dose) reduces food intake in diet-induced obese male C57BL/6 mice and specifically activates paraventricular nucleus neurons[1].
Notoginsenoside Fe (10 mg/kg; i.p.; daily; 6 days) has no effect on body weight, food intake, or hypothalamic neuron activation in healthy lean male C57BL/6 mice[1].

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

Animal Model: C57BL/6 mice with Obesity (male, 6 weeks old, diet-induced obesity model)[1]
Dosage: 10 mg/kg
Administration: i.p.; daily; 14 days
Result: Reduced body weight by 12% compared to untreated diet-induced obese mice.
Significantly decreased daily food intake.
Lowered fasting blood glucose.
Improved glucose tolerance, with reduced blood glucose levels at 60, 90, and 120 minutes following glucose injection.
Ameliorated hepatic steatosis, reduced hepatic triglyceride levels, and lowered serum alanine transaminase (ALT) levels compared to untreated obese mice.
Reduced adipose tissue adipocyte size and fat mass percentage, while increasing lean mass percentage relative to body weight.
Reduced mRNA expression levels of lipogenesis-related genes FAS, CD36, SREBP-1c, and MCP-1 in white adipose tissue.
Significantly increased oxygen consumption (VO2) and carbon dioxide production (VCO2) in both light and dark cycles, with no change in respiratory exchange ratio (RER).
Animal Model: C57BL/6 mice wiht Obesity (male, 6 weeks old, diet-induced obesity model, stereotaxic guide cannula implantation)[1]
Dosage: 5 mM in 2 μl per mouse
Administration: i.c.v.; single dose
Result: Significantly reduced food intake within 6 hours post-injection compared to saline-treated mice.
Induced a marked increase in C-Fos-positive neuron counts in the hypothalamic paraventricular nucleus (PVH), with no change in C-Fos expression in the arcuate nucleus (ARC).
Molecular Weight

917.13

Formula

C47H80O17

CAS No.
Appearance

Solid

Color

Light yellow to yellow

SMILES

C[C@]12[C@@](C)([C@]3([H])C[C@@H](O)[C@]1([H])[C@@]([H])([C@](C)(CC/C=C(C)/C)O[C@@H]4O[C@H](CO[C@@H]5O[C@@H](CO)[C@H](O)[C@H]5O)[C@@H](O)[C@H](O)[C@H]4O)CC2)CC[C@@]([C@]3(C)CC6)([H])C(C)(C)[C@H]6O[C@@]7([H])[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O7

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
Solvent & Solubility
In Vitro: 

H2O : 50 mg/mL (54.52 mM; Need ultrasonic)

DMSO : < 1 mg/mL (insoluble or slightly soluble)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 1.0904 mL 5.4518 mL 10.9036 mL
5 mM 0.2181 mL 1.0904 mL 2.1807 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

  • Molarity Calculator

  • Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only.If necessary, please contact MedChemExpress (MCE).
Purity & Documentation

Purity: 99.99%

References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
H2O 1 mM 1.0904 mL 5.4518 mL 10.9036 mL 27.2589 mL
5 mM 0.2181 mL 1.0904 mL 2.1807 mL 5.4518 mL
10 mM 0.1090 mL 0.5452 mL 1.0904 mL 2.7259 mL
15 mM 0.0727 mL 0.3635 mL 0.7269 mL 1.8173 mL
20 mM 0.0545 mL 0.2726 mL 0.5452 mL 1.3629 mL
25 mM 0.0436 mL 0.2181 mL 0.4361 mL 1.0904 mL
30 mM 0.0363 mL 0.1817 mL 0.3635 mL 0.9086 mL
40 mM 0.0273 mL 0.1363 mL 0.2726 mL 0.6815 mL
50 mM 0.0218 mL 0.1090 mL 0.2181 mL 0.5452 mL

* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Notoginsenoside Fe
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