QUERCITRIN

For Research Use Only.
Category
Flavonoids
Cat.No.
NP1828
CAS
522-12-3
Product Name
QUERCITRIN
Structure

Product Details

Description
Quercitrin isolated from the herb of Apocynum venetum L. Quercitrin and taxifolin promote osteoblast differentiation in MC3T3-E1 cells and also inhibit osteoclastogenesis in RAW264.7 cells, showing a positive effect of these flavonoids on bone metabolism.
Synonyms
Quercitrin; 3-[(-6-Deoxy-a-L-mannopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-1-benzopyran-4-one
IUPAC Name
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
Molecular Weight
448.38
Molecular Formula
C21H20O11
Canonical SMILES
CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O
InChI
1S/C21H20O11/c1-7-15(26)17(28)18(29)21(30-7)32-20-16(27)14-12(25)5-9(22)6-13(14)31-19(20)8-2-3-10(23)11(24)4-8/h2-7,15,17-18,21-26,28-29H,1H3/t7-,15-,17+,18+,21-/m0/s1
InChIKey
OXGUCUVFOIWWQJ-HQBVPOQASA-N
Boiling Point
477.14°C (rough estimate)
Melting Point
175-178 °C
Purity
0.99
Density
1.79g/cm3
Solubility
Soluble in DMSO
Appearance
Yellow powder
Application
antiviral; antispasmodic; diuretic; vasopressor; anti-inflammatory; antiproliferative and apoptotic effects; antibacterial
Shelf Life
As supplied, 2 years from the QC date provided on the Certificate of Analysis, when stored properly
Storage
Store at -20 °C
BRN
68135
Color
Yellow
Definition
ChEBI: A quercetin O-glycoside that is quercetin substituted by a alpha-L-rhamnosyl moiety at position 3 via a glycosidic linkage.
EINECS
208-322-5
F
10-23
Form
Powder
HS Code
29389090
Merck
8125
pKa
6.17±0.40(Predicted)
Refractive Index
1.5376 (estimate)
RTECS
UZ5950000
Safety Statements
24/25
Stability
Hygroscopic
WGK Germany
3
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