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Glycyroside

CAS# 125310-04-5

Glycyroside

Catalog No. BCX0656----Order now to get a substantial discount!

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Chemical structure

Glycyroside

Chemical Properties of Glycyroside

Cas No. 125310-04-5 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C27H30O13 M.Wt 562.52
Type of Compound N/A 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.

Glycyroside Dilution Calculator

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Glycyroside Molarity Calculator

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Preparing Stock Solutions of Glycyroside

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.7777 mL 8.8886 mL 17.7771 mL 35.5543 mL 44.4429 mL
5 mM 0.3555 mL 1.7777 mL 3.5554 mL 7.1109 mL 8.8886 mL
10 mM 0.1778 mL 0.8889 mL 1.7777 mL 3.5554 mL 4.4443 mL
50 mM 0.0356 mL 0.1778 mL 0.3555 mL 0.7111 mL 0.8889 mL
100 mM 0.0178 mL 0.0889 mL 0.1778 mL 0.3555 mL 0.4444 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 Glycyroside

Chemical constituents of Spatholobus suberectus.[Pubmed:23302527]

Chin J Nat Med. 2012 Jan;10(1):32-5.

AIM: To investigate chemical constituents of Spatholobus suberectus Dunn. METHODS: Isolation and purification were carried out by column chromatographic methods. Compounds were characterized based on their physical characteristics and spectra data. RESULTS: Seventeen compounds were isolated from ethanol extract of S. suberectus. The structures were elucidated as prestegane B (1), (2R, 3R)-buteaspermanol (2), (+)-medioresinol (3), (2R, 3R)-3,7-dihydroxyflavanone (4), benzeneethanol (5), 4, 7, 2'-trihydroxy-4'-methoxyisoflavanol (6), naringenin (7), blumenol A (8), protocatechuic acid ethyl ester (9), liquiritigenin (10), 7, 4'-dihydroxy-8-methoxy-isoflavone (11), 3, 5, 7, 3', 5'-pentahydroxyflavanone (12), protocatechuic acid (13), Glycyroside (14), 8-methylretusin-7-O-beta-D-glucopyranoside (15), 3, 3', 4', 5, 6, 7, 8-heptahydroxyflavan (16), and dulcisflavan (17). CONCLUSION: All compounds are firstly isolated from the title plant and compounds 1, 3 were isolated from the Spatholobus genus for the first time.

[Studies on chemical constituents of Glycyrrhiza eurycarpa P. C. Li].[Pubmed:2618694]

Yao Xue Xue Bao. 1989;24(7):525-31.

A species of the genus Glycyrrhiza, G. eurycarpa P. C. Li recently reported as a new species growing in Gansu Province and Xinjiang Autonomous Region has not been studied before on its chemical constituents. This paper reports the isolation and chemical elucidation of four flavonoid glycosides from this species collected in Jinta County, Gansu Province. On the basis of physical and chemical constants and spectroscopic data (UV, IR, MS, 1HNMR and 13CNMR), compound I was confirmed as a new isoflavone diglycoside. Its structure was elucidated as formononetin-7-O[-D-apio-beta-D-furanosyl(1----2)]-beta-D-gl ucopyranoside. The new compound was named Glycyroside. The other three components (II-IV) were identified as liquiritin, isoliquiritin and schaftoside, respectively.

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