HYPEROSIDE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C21H20O12
Molecular Weight	464.3763
Optical Activity	UNSPECIFIED
Defined Stereocenters	5 / 5
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

OC[C@H]1O[C@@H](OC2=C(OC3=C(C2=O)C(O)=CC(O)=C3)C4=CC=C(O)C(O)=C4)[C@H](O)[C@@H](O)[C@H]1O

InChI

InChIKey=OVSQVDMCBVZWGM-DTGCRPNFSA-N

InChI=1S/C21H20O12/c22-6-13-15(27)17(29)18(30)21(32-13)33-20-16(28)14-11(26)4-8(23)5-12(14)31-19(20)7-1-2-9(24)10(25)3-7/h1-5,13,15,17-18,21-27,29-30H,6H2/t13-,15+,17+,18-,21+/m1/s1

HIDE SMILES / InChI

Molecular Formula	C21H20O12
Molecular Weight	464.3763
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	5 / 5
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
A new flavonol glycoside gallate ester from Acer okamotoanum and its inhibitory activity against human immunodeficiency virus-1 (HIV-1) integrase.	1998 Jan	9461665
[HPLC investigation of antioxidant components in Solidago herba].	2004	16316050
Flavonoids and antiulcerogenic activity from Byrsonima crassa leaves extracts.	2005 Feb 10	15652267
Binding interaction of quercetin-3-beta-galactoside and its synthetic derivatives with SARS-CoV 3CL(pro): structure-activity relationship studies reveal salient pharmacophore features.	2006 Dec 15	17046271
[Studies on chemical constituentsfrom leaves of Acer truncatum].	2007 Aug	17972585
Constituents and antiulcer effect of Alchornea glandulosa: activation of cell proliferation in gastric mucosa during the healing process.	2007 Mar	17329837
The mechanism of hyperoside protection of ECV-304 cells against tert-butyl hydroperoxide-induced injury.	2008	18552516
[Studies on chemical constituents from Davidia involucrata var. vilmoriniana].	2008 Apr	18589778
Deconjugation and degradation of flavonol glycosides by pig cecal microbiota characterized by Fluorescence in situ hybridization (FISH).	2008 Mar 26	18303842
Phytochemicals of apple peels: isolation, structure elucidation, and their antiproliferative and antioxidant activities.	2008 Nov 12	18828600
Antioxidant and enzyme inhibition activities and chemical profiles of Polygonum sachalinensis F.Schmidt ex Maxim (Polygonaceae).	2010 Mar	19698767
Discovery of flavonoid derivatives as anti-HCV agents via pharmacophore search combining molecular docking strategy.	2012 Jun	22445328
Antiplasmodial activity of flavonol quercetin and its analogues in Plasmodium falciparum: evidence from clinical isolates in Bangladesh and standardized parasite clones.	2012 Jun	22215188

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 20:40:32 UTC 2023` Edited by `admin` on `Fri Dec 15 20:40:32 UTC 2023`
Record UNII	8O1CR18L82
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

HYPEROSIDE

Common Name

English

NSC-407304

Code

English

HYPEROSIDE [USP-RS]

Common Name

English

QUERCETIN 3-.BETA.-D-GALACTOPYRANOSIDE

Common Name

English

QUERCETIN-3-O-GALACTOSIDE

Common Name

English

HYPEROSID

Common Name

English

QUERCETIN 3-O-.BETA.-D-GALACTOSIDE

Systematic Name

English

HYPERIN

Common Name

English

HYPEROSIDE (CONSTITUENT OF HAWTHORN LEAF WITH FLOWER) [DSC]

Common Name

English

HYPEROSIDE (CONSTITUENT OF ST. JOHN'S WORT) [DSC]

Common Name

English

2-(3,4-DIHYDROXYPHENYL)-3-(.BETA.-D-GALACTOPYRANOSYLOXY)-5,7-DIHYDROXY-4H-1-BENZOPYRAN-4-ONE

Common Name

English

Classification Tree Code System Code

DSLD

1394 (Number of products:104)