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Astragaloside III

CAS# 84687-42-3

Astragaloside III

Catalog No. BCN5963----Order now to get a substantial discount!

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Astragaloside III: 5mg $98 In Stock
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Quality Control of Astragaloside III

Number of papers citing our products

Chemical structure

Astragaloside III

3D structure

Chemical Properties of Astragaloside III

Cas No. 84687-42-3 SDF Download SDF
PubChem ID 441905 Appearance White powder
Formula C41H68O14 M.Wt 784.97
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in methan
SMILES CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)O)C
Standard InChIKey FVFSMBDVZVUETN-BQAOMNQWSA-N
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Astragaloside III

The root of Astragalus membranaceus (Fisch.) Bunge

Biological Activity of Astragaloside III

DescriptionAstragaloside III has anti-gastric ulcer effects, and exhibits strong growth-promoting effects in cultured GES-1 cells. Astragaloside III can effectively reduce cancer cell survival in vitro and inhibit the tumor growth in vivo, the potential mechanism is the induction of cell apoptosis signaling pathways, suggests that it provides a new therapeutic tool to treat breast cancer.
In vitro

Effects of cycloartane saponins from hairy roots of Astragalus membranaceus Bge., on human tumor cell targets.[Pubmed: 20060881]

Fitoterapia. 2010 Jul;81(5):447-51.

For the first time three different natural compounds, isolated from hairy roots of Astragalus membranaceus, cultivated in airlift bioreactor were tested for their cytotoxic potential and apoptosis induction in a panel of human tumor cell lines.
METHODS AND RESULTS:
Root cultures, cultivated in bioreactor gave 18.5 g l(-1) dry wt roots with the highest astragaloside production in vitro up to now - 1.64% (astragaloside I), 1.12% (astragaloside II) and 1.08% (Astragaloside III).
CONCLUSIONS:
In this manner the production in airlift bioreactor can be used as means of reliable supply of cycloartane saponins to extend the research to human clinical studies.

In vivo

Astragaloside III from Astragalus membranaceus antagonizes breast cancer growth[Reference: WebLink]

Afr. J. Tradit. Complem., 2015, 12(3):183-6.

Astragaloside III has been used to treat different cancers; however their effect on breast cancer remains unknown.
METHODS AND RESULTS:
The present study examined the effects of Astragaloside III from Astragalus membranaceus on breast cancer cell lines in vitro as well as xenograft in vivo. The results showed that the Astragaloside III could effectively reduce cancer cell survival in vitro and inhibit the tumor growth in vivo. The potential mechanism is the induction of cell apoptosis signaling pathways.
CONCLUSIONS:
We believe that Astragaloside III provides a new therapeutic tool to treat breast cancer.

Protocol of Astragaloside III

Structure Identification
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Jun 1;960:43-51.

Component analysis and structure identification of active substances for anti-gastric ulcer effects in Radix Astragali by liquid chromatography and tandem mass spectrometry.[Pubmed: 24780704 ]

This study provided a comprehensive component analysis and structure identification of active substances for the anti-gastric ulcer effects of Radix Astragali.
METHODS AND RESULTS:
The data were generated by organically combining the results from in vivo pharmacodynamic experiments, a cell growth-promoting assay, structure identification, content determination, fingerprinting, and correlation analyses. The fingerprints from high-performance liquid chromatography coupled with a diode array detector (HPLC-DAD) and from HPLC coupled with evaporative light scattering detectors (ELSD) from 95% ethanol extracts of Radix Astragali (ERA) were determined using HPLC-DAD-ELSD. The structures of 16 compounds were identified using ultra-pressure liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS). The contents of these 16 compounds were simultaneously determined in a single run using HPLC-DAD-ELSD. The strength of the anti-ulceration effect of each of the 16 compounds was correlated to its content in the HPLC spectrum using gray relation statistics. The sequence of the contribution from each of the 16 compounds to the anti-gastric ulcer effect was determined. The results showed that ononin, astragalosideIII, and astragalosideIV contributed most to the observed anti-gastric ulcer effects and that these three compounds also exhibited strong growth-promoting effects in cultured GES-1 cells.
CONCLUSIONS:
The results of this study can be used to evaluate the quality of Radix Astragali and to provide a theoretical foundation for its further study.

Astragaloside III Dilution Calculator

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Astragaloside III Molarity Calculator

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Preparing Stock Solutions of Astragaloside III

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.2739 mL 6.3697 mL 12.7393 mL 25.4787 mL 31.8484 mL
5 mM 0.2548 mL 1.2739 mL 2.5479 mL 5.0957 mL 6.3697 mL
10 mM 0.1274 mL 0.637 mL 1.2739 mL 2.5479 mL 3.1848 mL
50 mM 0.0255 mL 0.1274 mL 0.2548 mL 0.5096 mL 0.637 mL
100 mM 0.0127 mL 0.0637 mL 0.1274 mL 0.2548 mL 0.3185 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

Organizitions Citing Our Products recently

 
 
 

Calcutta University

University of Minnesota

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The Ohio State University

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Worcester Polytechnic Institute

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The University of Tokyo
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Korea University
Korea University

Background on Astragaloside III

Astragaloside III is a natural product isolated from Astragalus.

References:
[1]. SHI Jing-chao, et al. Determination of Astragaloside Ⅲ and Astragaloside IV in Astragalus with HPLC-ELSD Method. World Journal of Integrated Traditional and Western Medicine, 2014-07

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References on Astragaloside III

Component analysis and structure identification of active substances for anti-gastric ulcer effects in Radix Astragali by liquid chromatography and tandem mass spectrometry.[Pubmed:24780704]

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Jun 1;960:43-51.

This study provided a comprehensive component analysis and structure identification of active substances for the anti-gastric ulcer effects of Radix Astragali. The data were generated by organically combining the results from in vivo pharmacodynamic experiments, a cell growth-promoting assay, structure identification, content determination, fingerprinting, and correlation analyses. The fingerprints from high-performance liquid chromatography coupled with a diode array detector (HPLC-DAD) and from HPLC coupled with evaporative light scattering detectors (ELSD) from 95% ethanol extracts of Radix Astragali (ERA) were determined using HPLC-DAD-ELSD. The structures of 16 compounds were identified using ultra-pressure liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS). The contents of these 16 compounds were simultaneously determined in a single run using HPLC-DAD-ELSD. The strength of the anti-ulceration effect of each of the 16 compounds was correlated to its content in the HPLC spectrum using gray relation statistics. The sequence of the contribution from each of the 16 compounds to the anti-gastric ulcer effect was determined. The results showed that ononin, astragalosideIII, and astragalosideIV contributed most to the observed anti-gastric ulcer effects and that these three compounds also exhibited strong growth-promoting effects in cultured GES-1 cells. The results of this study can be used to evaluate the quality of Radix Astragali and to provide a theoretical foundation for its further study.

Effects of cycloartane saponins from hairy roots of Astragalus membranaceus Bge., on human tumor cell targets.[Pubmed:20060881]

Fitoterapia. 2010 Jul;81(5):447-51.

For the first time three different natural compounds, isolated from hairy roots of Astragalus membranaceus, cultivated in airlift bioreactor were tested for their cytotoxic potential and apoptosis induction in a panel of human tumor cell lines. Root cultures, cultivated in bioreactor gave 18.5 g l(-1) dry wt roots with the highest astragaloside production in vitro up to now - 1.64% (astragaloside I), 1.12% (astragaloside II) and 1.08% (Astragaloside III). In this manner the production in airlift bioreactor can be used as means of reliable supply of cycloartane saponins to extend the research to human clinical studies.

Description

Astragaloside III is a natural product isolated from Astragalus.

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