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Ginsenoside Ra1
Ginsenoside Ra1, a component from ginseng, exhibits significant inhibitory effects on protein tyrosine kinase (PTK) activation induced by hypoxia/reoxygenation (H/R).
Catalog No. TN1096Cas No. 83459-41-0
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Purity:97.44%
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Ginsenoside Ra1
Catalog No. TN1096Cas No. 83459-41-0
Ginsenoside Ra1, a component from ginseng, exhibits significant inhibitory effects on protein tyrosine kinase (PTK) activation induced by hypoxia/reoxygenation (H/R).
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose. | Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $115 | In Stock | |
| 5 mg | $280 | In Stock | |
| 10 mg | Inquiry | In Stock |
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Bioactivity
Chemical Properties
| Description | Ginsenoside Ra1, a component from ginseng, exhibits significant inhibitory effects on protein tyrosine kinase (PTK) activation induced by hypoxia/reoxygenation (H/R). |
| In vitro | Ginsenoside Ra1 showed significant inhibitory effects on protein tyrosine kinase (PTK) activation induced by an in vitro hypoxia/reoxygenation (H/R) model in cultured human umbilical vein endothelial cells (HUVEC)[1]. |
| Molecular Weight | 1211.38 |
| Formula | C58H98O26 |
| Cas No. | 83459-41-0 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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(mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.Preparation method for in vivo formula: Take 50 μL DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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