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Glyurallin B

CAS# 199331-53-8

Glyurallin B

2D Structure

Catalog No. BCX0963----Order now to get a substantial discount!

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3D structure

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Glyurallin B

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Chemical Properties of Glyurallin B

Cas No. 199331-53-8 SDF Download SDF
PubChem ID 15818599.0 Appearance Powder
Formula C25H26O6 M.Wt 422.17
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 3-[3,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-8-(3-methylbut-2-enyl)chromen-4-one
SMILES CC(=CCC1=C(C(=CC(=C1)C2=COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)O)O)C
Standard InChIKey DPLWUTYEBRKBLI-UHFFFAOYSA-N
Standard InChI InChI=1S/C25H26O6/c1-13(2)5-7-15-9-16(10-21(28)23(15)29)18-12-31-25-17(8-6-14(3)4)19(26)11-20(27)22(25)24(18)30/h5-6,9-12,26-29H,7-8H2,1-4H3
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.

Glyurallin B Dilution Calculator

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Glyurallin B Molarity Calculator

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Preparing Stock Solutions of Glyurallin B

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.3687 mL 11.8436 mL 23.6871 mL 47.3743 mL 59.2179 mL
5 mM 0.4737 mL 2.3687 mL 4.7374 mL 9.4749 mL 11.8436 mL
10 mM 0.2369 mL 1.1844 mL 2.3687 mL 4.7374 mL 5.9218 mL
50 mM 0.0474 mL 0.2369 mL 0.4737 mL 0.9475 mL 1.1844 mL
100 mM 0.0237 mL 0.1184 mL 0.2369 mL 0.4737 mL 0.5922 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 Glyurallin B

Antioxidant and anti-inflammatory activities of six flavonoids separated from licorice.[Pubmed:23790887]

Food Chem. 2013 Nov 15;141(2):1063-71.

Licorice, the roots and rhizomes of several Glycyrrhiza species (Leguminosae), is an important natural sweetening agent and a widely used herbal medicine. In this work, six flavonoids, 5-(1,1-dimethylallyl)-3,4,4'-trihydroxy-2-methoxychalcone (1), licochalcone B (2), licochalcone A (3), echinatin (4), glycycoumarin (5) and Glyurallin B (6), were isolated from the extracts of licorice (Glycyrrhiza inflata and Glycyrrhiza uralensis). Their structures were elucidated using various spectroscopic methods. To our knowledge, compound 1 was isolated from natural plants for the first time. All the isolates were tested by antioxidant and anti-inflammatory assays. Compounds 2, 4 and 5 showed strong scavenging activity toward the ABTS(+) radical, and compounds 1, 2, 3, 5 and 6 exhibited potent inhibition of lipid peroxidation in rat liver microsomes compared with the reference controls. Compounds 1-4 dose-dependently inhibited LPS induced reactive oxygen species (ROS) production in RAW 264.7 cells. Furthermore, compounds 1-5 were demonstrated to inhibit the production of nitric oxide (NO), interleukin-6 (IL-6) and prostaglandin E2 (PGE2) in LPS-induced macrophage cells. Moreover, the contents of the six compounds, in different Glycyrrhiza species, were quantified by HPLC-MS.

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