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Quercetin 3-O-robinobioside

CAS# 52525-35-6

Quercetin 3-O-robinobioside

Catalog No. BCN5676----Order now to get a substantial discount!

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Chemical structure

Quercetin 3-O-robinobioside

3D structure

Chemical Properties of Quercetin 3-O-robinobioside

Cas No. 52525-35-6 SDF Download SDF
PubChem ID 10371536 Appearance Yellow powder
Formula C27H30O16 M.Wt 610.5
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one
SMILES CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O
Standard InChIKey IKGXIBQEEMLURG-IEBISRBZSA-N
Standard InChI InChI=1S/C27H30O16/c1-8-17(32)20(35)22(37)26(40-8)39-7-15-18(33)21(36)23(38)27(42-15)43-25-19(34)16-13(31)5-10(28)6-14(16)41-24(25)9-2-3-11(29)12(30)4-9/h2-6,8,15,17-18,20-23,26-33,35-38H,7H2,1H3/t8-,15+,17-,18-,20+,21-,22+,23+,26+,27-/m0/s1
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 Quercetin 3-O-robinobioside

The herbs of Callicarpa bodinieri Levl.

Biological Activity of Quercetin 3-O-robinobioside

Description1.Quercetin-3-O-robinobioside is a quercetin-derived flavonol, exhibits antioxidant activities. 2.Quercetin-3-O-robinobioside exhibits in-vitro inhibitory activities against leukemia K562 cells.

Quercetin 3-O-robinobioside Dilution Calculator

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Preparing Stock Solutions of Quercetin 3-O-robinobioside

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.638 mL 8.19 mL 16.38 mL 32.76 mL 40.95 mL
5 mM 0.3276 mL 1.638 mL 3.276 mL 6.552 mL 8.19 mL
10 mM 0.1638 mL 0.819 mL 1.638 mL 3.276 mL 4.095 mL
50 mM 0.0328 mL 0.1638 mL 0.3276 mL 0.6552 mL 0.819 mL
100 mM 0.0164 mL 0.0819 mL 0.1638 mL 0.3276 mL 0.4095 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 Quercetin 3-O-robinobioside

[Chemical constituents and antitumor activity on leukemia K562 cell of Leonurus heterophyllus].[Pubmed:19894515]

Zhongguo Zhong Yao Za Zhi. 2009 Jul;34(14):1816-8.

The chemical constituents of Leonurus heterophyllus were separated and purified by repeated column chromatography on silica gel, HPD 100, Sephadex LH-20, and PHPLC. Each compound was characterized by spectroscopic and physical data. Eight compounds have been purified and identified to be Quercetin 3-O-robinobioside (1), rutin (2), isoquerci trin (3), hyperoside (4), quercetin (5), apigenin (6), genkwanin (7), and benzoic acid (8). Among them, compounds 2, 5-7 were isolated from L. heterophyllus for the first time; Compounds 1, 3, 4, 8 were obtained for the first time from the genus Leonurus. The in vitro activities against leukemia K562 Cells of pure components were evaluated by testing their IC50. Compounds 1-6, 8 exhibited in-vitro inhibitory activities against leukemia K562 cells in different extent.

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