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CAS RN: 62025-49-4 | Product Number: G0581
Ginsenoside F2
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Purity: >95.0%(HPLC)
Synonyms:
- (3β,12β)-12-Hydroxydammar-24-ene-3,20-diyl Bis-β-D-glucopyranoside
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
|
|---|---|---|---|---|---|
| 25MG |
₩337,400
|
0 | 0 | Contact Us |
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* The storage conditions are subject to change without notice.
* The storage conditions are subject to change without notice.
| Product Number | G0581 |
Purity / Analysis Method 
|
>95.0%(HPLC) |
| Molecular Formula / Molecular Weight | C__4__2H__7__2O__1__3 = 785.03 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature
|
Refrigerated (0-10°C) |
| Condition to Avoid | Heat Sensitive |
| CAS RN | 62025-49-4 |
| Reaxys Registry Number | 5720814 |
| PubChem Substance ID | 468591948 |
| MDL Number | MFCD06410948 |
Specifications
| Appearance | White to Almost white powder to crystal |
| Purity(HPLC) | min. 95.0 area% |
| Melting point | 183.0 to 187.0 °C |
| Specific rotation | +30.0 to +33.0 deg(C=0.5, methanol) |
| NMR | confirm to structure |
Properties (reference)
| Melting Point | 185 °C |
GHS
Related Laws:
| RTECS# | LZ5901200 |
Transport Information:
| H.S.code* | 2938.90-000 |
Application
Ginsenoside F2: A Ginsenoiside with Diverse Biological Activities
Ginsenoside F2 is a minor ginsenoiside that has been found in Panax ginseng and has diverse biological activities, including anticancer effects.1-4) Ginsenoside F2 is also produced by hydrolysis of ginsenoside Rb1 which is the most predominant ginsenoside in Panax ginseng.5) (The product is for research purpose only.)
References
- 1) Ginsenoside F2 induces apoptosis accompanied by protective autophagy in breast cancer stem cells
- 2) Anti-cancer effect of ginsenoside F2 against glioblastoma multiforme in xenograft model in SD rats
- 3) Ginsenoside F2 possesses anti-obesity activity via binding with PPARγ and inhibiting adipocyte differentiation in the 3T3-L1 cell line
- 4) The inductive effect of ginsenoside F2 on hair growth by altering the WNT signal pathway in telogen mouse skin
- 5) Conversion of Major Ginsenoside Rb1 to Ginsenoside F2 by Caulobacter leidyia
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