Achyranthoside C

CAS# 168009-90-3

Achyranthoside C

Catalog No. BCN8988----Order now to get a substantial discount!

Product Name & Size Price Stock
Achyranthoside C: 5mg $339 In Stock
Achyranthoside C: 10mg Please Inquire In Stock
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Quality Control of Achyranthoside C

Number of papers citing our products

Chemical structure

Achyranthoside C

Chemical Properties of Achyranthoside C

Cas No. 168009-90-3 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C47H72O20 M.Wt 957.1
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
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 Achyranthoside C

The roots of Achyranthes bidentata Blume.

Achyranthoside C Dilution Calculator

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Achyranthoside C Molarity Calculator

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Preparing Stock Solutions of Achyranthoside C

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.0448 mL 5.2241 mL 10.4482 mL 20.8965 mL 26.1206 mL
5 mM 0.209 mL 1.0448 mL 2.0896 mL 4.1793 mL 5.2241 mL
10 mM 0.1045 mL 0.5224 mL 1.0448 mL 2.0896 mL 2.6121 mL
50 mM 0.0209 mL 0.1045 mL 0.209 mL 0.4179 mL 0.5224 mL
100 mM 0.0104 mL 0.0522 mL 0.1045 mL 0.209 mL 0.2612 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.

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References on Achyranthoside C

Inhibitory effects of three oleanolic acid glycosides from Achyranthes japonica on the complement classical pathway.[Pubmed:21770839]

Immunopharmacol Immunotoxicol. 2012 Apr;34(2):213-5.

The present study evaluated the anticomplement effects of isolated compounds from Achyranthes japonica in the classical pathway of the complement system. Using column chromatography, three compounds: Achyranthoside C dimethyl ester, Achyranthoside C butyl dimethyl ester, and achyranthoside E dimethyl ester were isolated and evaluated for in vitro anticomplement activity. Achyranthoside C dimethyl ester showed the most potent inhibitory activity against the complement system, with 50% inhibitory concentrations (IC(50)) values of 26.2 mug/mL. This is the first report of anticomplement activity of isolated compounds from A. japonica.

Five new oleanolic acid glycosides from Achyranthes bidentata with inhibitory activity on osteoclast formation.[Pubmed:16041655]

Planta Med. 2005 Jul;71(7):673-9.

Bioassay-directed fractionation of a butanol-soluble fraction of methanol extract of the root of Achyranthes bidentata resulted in the isolation of 5 new oleanolic acid glycosides 1-5, namely, 18-(beta-D-glucopyranosyloxy)-28-oxoolean-12-en-3beta-yl 3-O-(beta-D-glucopyranosyl)-beta-D-glucopyranosiduronic acid methyl ester (1), Achyranthoside C dimethyl ester (2), Achyranthoside C butyl dimethyl ester (3), achyranthoside E dimethyl ester (4), and achyranthoside E butyl methyl ester (5), together with 10 known compounds. Their structures were established on the basis of spectroscopic interpretation and chemical methods. All the oleanolic acid glycosides inhibited the formation of osteoclast-like multinucleated cells (OCLs) induced by 1alpha,25(OH)2D3 in a co-culture assay system.

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