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Anemarrhenasaponin I

Catalog No. TQ0036Cas No. 163047-21-0

Anemarrhenasaponin I shows the remarkable inhibiting effect on platelet aggregation.

Anemarrhenasaponin I

Anemarrhenasaponin I

Purity: 99.85%
Catalog No. TQ0036Cas No. 163047-21-0
Anemarrhenasaponin I shows the remarkable inhibiting effect on platelet aggregation.
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5 mg$74In Stock
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Purity:99.85%
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Product Introduction

Bioactivity
Description
Anemarrhenasaponin I shows the remarkable inhibiting effect on platelet aggregation.
Chemical Properties
Molecular Weight758.93
FormulaC39H66O14
Cas No.163047-21-0
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 50 mg/mL (65.88 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.3176 mL6.5882 mL13.1764 mL65.8822 mL
5 mM0.2635 mL1.3176 mL2.6353 mL13.1764 mL
10 mM0.1318 mL0.6588 mL1.3176 mL6.5882 mL
20 mM0.0659 mL0.3294 mL0.6588 mL3.2941 mL
50 mM0.0264 mL0.1318 mL0.2635 mL1.3176 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent 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 DMSOTargetMol | reagent (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 DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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