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Isosaponarin

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Catalog No. T4430Cas No. 19416-87-6

Isosaponarin is a natural product with multiple activities. It inhibits the increase in Ca2+ levels induced by 4-aminopyridine in rat synaptosomes without affecting the membrane potential of synaptosomes, while reducing the phosphorylation of PKC, PKCα, SNAP-25, and MARCKS, thereby inhibiting the release of glutamate from vesicles in synaptosomes.

Isosaponarin

Isosaponarin

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Purity: 99.12%
Catalog No. T4430Cas No. 19416-87-6
Isosaponarin is a natural product with multiple activities. It inhibits the increase in Ca2+ levels induced by 4-aminopyridine in rat synaptosomes without affecting the membrane potential of synaptosomes, while reducing the phosphorylation of PKC, PKCα, SNAP-25, and MARCKS, thereby inhibiting the release of glutamate from vesicles in synaptosomes.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$280-In Stock
5 mg$789-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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.
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Purity:99.12%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
Isosaponarin is a natural product with multiple activities. It inhibits the increase in Ca2+ levels induced by 4-aminopyridine in rat synaptosomes without affecting the membrane potential of synaptosomes, while reducing the phosphorylation of PKC, PKCα, SNAP-25, and MARCKS, thereby inhibiting the release of glutamate from vesicles in synaptosomes.
In vitro
Methods:
Human fibroblasts were treated with Isosaponarin at concentrations of 0.001–0.1 μg/mL for 24 hours to evaluate its effects on collagen synthesis and the expression of related proteins.
Results:
Isosaponarin promoted collagen synthesis, which was closely associated with the upregulation of TβR-II and P4H production. [1]
In vivo
Methods:
A single oral dose of 50 mg/kg Isosaponarin was administered to 6-week-old female ICR mice to investigate its intestinal metabolism as well as absorption and excretion in the body.
Results:
Isosaponarin was metabolized to Isovitexin in the intestine, and most of it was not absorbed but excreted via feces. [2]
Chemical Properties
Molecular Weight594.52
FormulaC27H30O15
Cas No.19416-87-6
SmilesOC1=C2C(OC(=CC2=O)C3=CC=C(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)C=C3)=CC(O)=C1[C@@H]5O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O
Relative Density.1.723g/cm3
Storage & Solubility Information
Storagekeep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 100 mg/mL (168.2 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.6820 mL8.4101 mL16.8203 mL84.1015 mL
5 mM0.3364 mL1.6820 mL3.3641 mL16.8203 mL
10 mM0.1682 mL0.8410 mL1.6820 mL8.4101 mL
20 mM0.0841 mL0.4205 mL0.8410 mL4.2051 mL
50 mM0.0336 mL0.1682 mL0.3364 mL1.6820 mL
100 mM0.0168 mL0.0841 mL0.1682 mL0.8410 mL

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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%
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