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Myricetin 3-O-beta-D-glucopyranoside

CAS# 19833-12-6

Myricetin 3-O-beta-D-glucopyranoside

Catalog No. BCN8144----Order now to get a substantial discount!

Product Name & Size Price Stock
Myricetin 3-O-beta-D-glucopyranoside:5mg Please Inquire In Stock
Myricetin 3-O-beta-D-glucopyranoside:10mg Please Inquire In Stock
Myricetin 3-O-beta-D-glucopyranoside:20mg Please Inquire In Stock
Myricetin 3-O-beta-D-glucopyranoside:50mg Please Inquire In Stock
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Quality Control of Myricetin 3-O-beta-D-glucopyranoside

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Chemical structure

Myricetin 3-O-beta-D-glucopyranoside

3D structure

Chemical Properties of Myricetin 3-O-beta-D-glucopyranoside

Cas No. 19833-12-6 SDF Download SDF
PubChem ID 5318606 Appearance Powder
Formula C21H20O13 M.Wt 480.4
Type of Compound Flavonoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one
SMILES C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O
Standard InChIKey FOHXFLPXBUAOJM-LIBJPBHASA-N
Standard InChI InChI=1S/C21H20O13/c22-5-12-15(28)17(30)18(31)21(33-12)34-20-16(29)13-8(24)3-7(23)4-11(13)32-19(20)6-1-9(25)14(27)10(26)2-6/h1-4,12,15,17-18,21-28,30-31H,5H2/t12-,15-,17+,18-,21+/m1/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 Myricetin 3-O-beta-D-glucopyranoside

The root bark of Myrica cerifera L.

Biological Activity of Myricetin 3-O-beta-D-glucopyranoside

Description1. Myricetin 3-O-beta-D-glucopyranoside may have antioxidant, and anti-inflammatory activities.
TargetsImmunology & Inflammation related

Myricetin 3-O-beta-D-glucopyranoside Dilution Calculator

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Myricetin 3-O-beta-D-glucopyranoside Molarity Calculator

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Preparing Stock Solutions of Myricetin 3-O-beta-D-glucopyranoside

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.0816 mL 10.408 mL 20.816 mL 41.632 mL 52.04 mL
5 mM 0.4163 mL 2.0816 mL 4.1632 mL 8.3264 mL 10.408 mL
10 mM 0.2082 mL 1.0408 mL 2.0816 mL 4.1632 mL 5.204 mL
50 mM 0.0416 mL 0.2082 mL 0.4163 mL 0.8326 mL 1.0408 mL
100 mM 0.0208 mL 0.1041 mL 0.2082 mL 0.4163 mL 0.5204 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 Myricetin 3-O-beta-D-glucopyranoside

Antioxidant activities and phytochemicals of leaf extracts from 10 native rhododendron species in taiwan.[Pubmed:24987425]

Evid Based Complement Alternat Med. 2014;2014:283938.

Rhododendron, one of the most famous ornamental plants in the world, is traditionally a medicinal plant. However, the potential bioactivities of native Rhododendron in Taiwan have not been completely studied. In this study, the results revealed that Rhododendron pseudochrysanthum exhibited the best antioxidant activities among 10 native Rhododendron species in Taiwan. Furthermore, based on a bioactivity-guided isolation principle, nine specific phytochemicals were isolated and identified as (2R,3S)-catechin (1), (2R,3R)-epicatechin (1'), (2R,3R)-dihydromyricetin 3-O- beta -l-arabinopyranoside (2), (2S,3S)-taxifolin 3-O- beta -l-arabinopyranoside (2'), (2R,3R)-taxifolin 3-O- beta -l-arabinopyranoside (3), myricetin 3-O- beta -d-glucopyranoside (3'), rutin (4), hyperoside (5), and quercitrin (6). Of these compounds, 2 and 3 were found to be major bioactive compounds, and their concentrations in the n-butanol (BuOH) fraction were determined to be 52.0 and 67.3 mg per gram, respectively. These results demonstrated that methanolic extracts of Rhododendron pseudochrysanthum leaves have excellent antioxidant activities and great potential as a source for natural health products.

An extract of Lannea microcarpa: composition, activity and evaluation of cutaneous irritation in cell cultures and reconstituted human epidermis.[Pubmed:16805959]

J Pharm Pharmacol. 2006 Jul;58(7):981-8.

Lannea microcarpa (Anacardiaceae) is a tropical tree used in African folk medicine and commercial dermopharmaceutical formulations. Fractionation and analysis of its polar extract allowed the identification of 4'-methoxy-myricetin 3-O-alpha-L-rhamnopyranoside, myricetin 3-O-alpha-L-rhamnopyranoside, Myricetin 3-O-beta-D-glucopyranoside, vitexin, isovitexin, gallic acid and epi-catechin, as the major constituents. In-vivo assay (the croton oil ear test in mice) showed that the extract had significant anti-inflammatory effect (ID50 = 900 microg cm(-2)) but ten times lower than that of indometacin (ID50 = 93 microg cm(-2)), the non-steroidal anti-inflammatory drug used as reference. Cytotoxicity and cutaneous irritation of the extract and its constituents were investigated. The crude extract and its major components did not affect cell viability in-vitro either in three different cultures (J774. A1, WEHI-164 and HEK-293) of cells grown in monolayers or in the reconstituted human epidermis (RHE, 3D model), nor did they cause release of pro-inflammatory mediators (IL-1alpha) or histomorphological modification of RHE.

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