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Tangshenoside I
🥰Excellent
Catalog No. TN5094Cas No. 117278-74-7
Tangshenoside I is a natural product isolated from Codonopsis pilosula, which may be related to the its hematopoietic and immune functions and has a weak α-glucosidase inhibitory activity.
Tangshenoside I
🥰Excellent
Catalog No. TN5094Cas No. 117278-74-7
Tangshenoside I is a natural product isolated from Codonopsis pilosula, which may be related to the its hematopoietic and immune functions and has a weak α-glucosidase inhibitory activity.
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Product Introduction
Bioactivity
Chemical Properties
| Description | Tangshenoside I is a natural product isolated from Codonopsis pilosula, which may be related to the its hematopoietic and immune functions and has a weak α-glucosidase inhibitory activity. |
| Molecular Weight | 678.63 |
| Formula | C29H42O18 |
| Cas No. | 117278-74-7 |
| Smiles | O(C1=C(OC)C=C(/C=C/COC(C[C@@](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)(CC(O)=O)C)=O)C=C1OC)[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O |
| Relative Density. | 1.55 g/cm3 (Predicted) |
Storage & Solubility Information
| Storage | 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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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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