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Isosaponarin

Name: Isosaponarin
Brand: TargetMol
SKU: T4430
Price: 280 USD
Availability: InStock
Rating: 5 (10 reviews)

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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

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Purity: 99.12%

Catalog No. T4430Cas No. 19416-87-6

Pack Size	Price	Availability	Quantity
1 mg	$280	In Stock
5 mg	$789	In Stock

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Purity:99.12%

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COA HNMR LCMS

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 Weight	594.52
Formula	C₂₇H₃₀O₁₅
Cas No.	19416-87-6
Smiles	OC1=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

Storage

keep 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

	1mg	5mg	10mg	50mg
1 mM	1.6820 mL	8.4101 mL	16.8203 mL	84.1015 mL
5 mM	0.3364 mL	1.6820 mL	3.3641 mL	16.8203 mL
10 mM	0.1682 mL	0.8410 mL	1.6820 mL	8.4101 mL
20 mM	0.0841 mL	0.4205 mL	0.8410 mL	4.2051 mL
50 mM	0.0336 mL	0.1682 mL	0.3364 mL	1.6820 mL
100 mM	0.0168 mL	0.0841 mL	0.1682 mL	0.8410 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 mother liquor preparation method and in vivo formula preparation method:

For 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% Saline/PBS/ddH₂O. So your working solution concentration is 2 mg/mL。

Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSO TargetMol | 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 DMSO TargetMol | reagent

main solution, add 300 μLPEG300 TargetMol | reagent

mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH₂O TargetMol | reagent

mix well and clarify

For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.

Dose Conversion

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc