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Roseoside
😃Good
Catalog No. TN4918Cas No. 54835-70-0
Alias Roseoside A, (6S,9R)-roseoside
Roseoside ((6S,9R)-roseoside), a sesquiterpenoid isolated from Catharanthus roseus, has strong antioxidant and proinsulinic activity, inhibits lipid oxidation, enhances insulin release from the β-cell line INS-1, and can be used in cancer research.
Roseoside
😃Good
Catalog No. TN4918Alias Roseoside A, (6S,9R)-roseosideCas No. 54835-70-0
Roseoside ((6S,9R)-roseoside), a sesquiterpenoid isolated from Catharanthus roseus, has strong antioxidant and proinsulinic activity, inhibits lipid oxidation, enhances insulin release from the β-cell line INS-1, and can be used in cancer research.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 5 mg | $1,520 | 7-10 days | |
| 1 mL x 10 mM (in DMSO) | $1,628 | 7-10 days |
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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.Product Introduction
Bioactivity
Chemical Properties
| Description | Roseoside ((6S,9R)-roseoside), a sesquiterpenoid isolated from Catharanthus roseus, has strong antioxidant and proinsulinic activity, inhibits lipid oxidation, enhances insulin release from the β-cell line INS-1, and can be used in cancer research. |
| In vitro | H9C2 cells were stimulated with 300 nM Ang II for 7 hours, with pre-treatment to the cells with NA, telmisartan, ginsenoside, roseoside (Roseoside), icariin E4 (IE4), or a combination of both components (Roseoside and IE4) 1 hour before Ang II stimulation. Pre-treatment with the combination of Roseoside and IE4 (1:1) decreased or increased the expression of all hypertensive-related molecules compared to each single component, revealing the synergistic effect of the two compounds[1]. |
| Alias | Roseoside A, (6S,9R)-roseoside |
| Molecular Weight | 386.44 |
| Formula | C19H30O8 |
| Cas No. | 54835-70-0 |
| Smiles | C(=C/[C@H](O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C)\[C@]2(O)C(C)(C)CC(=O)C=C2C |
| Relative Density. | 1.32 g/cm3 (Predicted) |
Storage & Solubility Information
| Storage | store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO (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.
(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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