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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 of HYPEROSIDE

SMILES

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

PubMed

TitleDatePubMed
Estrogenic/antiestrogenic activities of a Epimedium koreanum extract and its major components: in vitro and in vivo studies.
2012-08
Discovery of flavonoid derivatives as anti-HCV agents via pharmacophore search combining molecular docking strategy.
2012-06
Antiplasmodial activity of flavonol quercetin and its analogues in Plasmodium falciparum: evidence from clinical isolates in Bangladesh and standardized parasite clones.
2012-06
Phenolic compounds in leaves of Alchornea triplinervia: anatomical localization, mutagenicity, and antibacterial activity.
2010-08
[Chemical constituents of Laggera pterodonta].
2010-03
Antioxidant and enzyme inhibition activities and chemical profiles of Polygonum sachalinensis F.Schmidt ex Maxim (Polygonaceae).
2010-03
Effect of flavonoids from Exellodendron coriaceum (Chrysobalanaceae) on glucose-6-phosphatase.
2009-12
DOSY NMR applied to analysis of flavonoid glycosides from Bidens sulphurea.
2009-12
The constituents and their bioactivities of Houttuynia cordata.
2009-11
A new dihydrodibenzodioxinone from Hypericum x 'Hidcote'.
2009-06
Phytochemicals of apple peels: isolation, structure elucidation, and their antiproliferative and antioxidant activities.
2008-11-12
[Studies on chemical constituents from Davidia involucrata var. vilmoriniana].
2008-04
Deconjugation and degradation of flavonol glycosides by pig cecal microbiota characterized by Fluorescence in situ hybridization (FISH).
2008-03-26
The mechanism of hyperoside protection of ECV-304 cells against tert-butyl hydroperoxide-induced injury.
2008
[Studies on chemical constituentsfrom leaves of Acer truncatum].
2007-08
Mutagenic evaluation and chemical investigation of Byrsonima intermedia A. Juss. leaf extracts.
2007-06-13
Constituents and antiulcer effect of Alchornea glandulosa: activation of cell proliferation in gastric mucosa during the healing process.
2007-03
In silico prediction of pregnane X receptor activators by machine learning approaches.
2007-01
Binding interaction of quercetin-3-beta-galactoside and its synthetic derivatives with SARS-CoV 3CL(pro): structure-activity relationship studies reveal salient pharmacophore features.
2006-12-15
Constituents from the leaves of Phellodendron amurense and their antioxidant activity.
2006-09
Mutagenic activity promoted by amentoflavone and methanolic extract of Byrsonima crassa Niedenzu.
2006-08-01
3-O-beta-D-Galactopyranoside of quercetin as an active principle from high altitude Podophyllum hexandrum and evaluation of its radioprotective properties.
2005-12-03
Flavonoids and antiulcerogenic activity from Byrsonima crassa leaves extracts.
2005-02-10
Antioxidant activity of anthraquinones and flavonoids from flower of Reynoutria sachalinensis.
2005-01
Anti-HIV protease activity from rosa family plant extracts and rosamultin from Rosa rugosa.
2005
The protozoan Tetrahymena as a bioindicator to screen bioactive substances.
2004-11
Application of preparative high-speed counter-current chromatography for the separation of flavonoids from the leaves of Byrsonima crassa Niedenzu (IK).
2004-04-30
Depsides from the petals of Papaver rhoeas.
2004-04
[HPLC investigation of antioxidant components in Solidago herba].
2004
Herbal remedies of Solidago--correlation of phytochemical characteristics and antioxidative properties.
2003-08-08
Isolation and characterization of antioxidant phenolic compounds from the aerial parts of Hypericum hyssopifolium L. by activity-guided fractionation.
2003-07
Study on the inhibitory effects of Korean medicinal plants and their main compounds on the 1,1-diphenyl-2-picrylhydrazyl radical.
2003
St. John's wort induces hepatic drug metabolism through activation of the pregnane X receptor.
2000-06-20
A search for anti-viral properties in Panamanian medicinal plants. The effects on HIV and its essential enzymes.
1999-01
A new flavonol glycoside gallate ester from Acer okamotoanum and its inhibitory activity against human immunodeficiency virus-1 (HIV-1) integrase.
1998-01
Inhibition of HIV infection by flavanoids.
1993-10
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 20:13:38 GMT 2025
Edited
by admin
on Mon Mar 31 20:13:38 GMT 2025
Record UNII
8O1CR18L82
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-407304
Preferred Name English
HYPEROSIDE
USP-RS  
Common Name 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)
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
DSLD 4101 (Number of products:1)
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
Code System Code Type Description
FDA UNII
8O1CR18L82
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
PRIMARY
RS_ITEM_NUM
1335202
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
PRIMARY
PUBCHEM
5281643
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-580-6
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
PRIMARY
EPA CompTox
DTXSID501028789
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
PRIMARY
CAS
482-36-0
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
PRIMARY
CHEBI
67486
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
PRIMARY
NSC
407304
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
PRIMARY
MESH
C021304
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
PRIMARY
WIKIPEDIA
HYPEROSIDE
Created by admin on Mon Mar 31 20:13:38 GMT 2025 , Edited by admin on Mon Mar 31 20:13:38 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
Secondary metabolite detected in developing cacao seeds.