Description
(+)-Catechin 7-O-β-D-xylopyranoside is a glycosylated derivative of catechin, where a β-D-xylopyranose sugar moiety is attached to the 7th position of the (+)-catechin molecule via an O-glycosidic bond. This compound belongs to the flavonoid family and retains the antioxidant properties of catechin, while the glycosylation may enhance its solubility, stability, and bioavailability. It is naturally found in plants such as tea and certain fruits, and its structure consists of the catechin backbone with a xylose unit, contributing to potential health benefits such as antioxidant, anti-inflammatory, and cardioprotective effects.
Synonyms
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-3,5-dihydroxy-2H-1-benzopyran-7-yl β-D-xylopyranoside; β-D-Xylopyranoside, 2-(3,4-dihydroxyphenyl)-3,4-dihydro-3,5-dihydroxy-2H-1-benzopyran-7-yl, (2R-trans)-; (+)-Catechin 7-β-D-xylopyranoside; (+)-Catechol 7-β-D-xylopyranoside; Catechin-7-O-β-D-xylopyranoside; NSC 115491; Catechin 7-O-xyloside
Molecular Formula
C20H22O10
Canonical SMILES
C1[C@@H]([C@H](OC2=CC(=CC(=C21)O)O[C@H]3[C@@H]([C@H]([C@@H](CO3)O)O)O)C4=CC(=C(C=C4)O)O)O
InChI
InChI=1S/C20H22O10/c21-11-2-1-8(3-13(11)23)19-14(24)6-10-12(22)4-9(5-16(10)30-19)29-20-18(27)17(26)15(25)7-28-20/h1-5,14-15,17-27H,6-7H2/t14-,15+,17-,18+,19+,20-/m0/s1
InChIKey
UQKKDJWFQBNZBJ-MLYGIHNMSA-N
Boiling Point
773.7±60.0 °C at 760 mmHg
Solubility
Soluble in Acetone, Chloroform, Dichloromethane, DMSO, Ethyl Acetate