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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H20O12
Molecular Weight 464.3771
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HYPEROSIDE

SMILES

c1cc(c(cc1-c2c(c(=O)c3c(cc(cc3o2)O)O)O[C@@]4([H])[C@@]([H])([C@]([H])([C@]([H])([C@@]([H])(CO)O4)O)O)O)O)O

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 464.3771
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
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
[Studies on chemical constituentsfrom leaves of Acer truncatum].
2007 Aug
In silico prediction of pregnane X receptor activators by machine learning approaches.
2007 Jan
[Studies on chemical constituents from Davidia involucrata var. vilmoriniana].
2008 Apr
Effect of flavonoids from Exellodendron coriaceum (Chrysobalanaceae) on glucose-6-phosphatase.
2009 Dec
The constituents and their bioactivities of Houttuynia cordata.
2009 Nov
Phenolic compounds in leaves of Alchornea triplinervia: anatomical localization, mutagenicity, and antibacterial activity.
2010 Aug
[Chemical constituents of Laggera pterodonta].
2010 Mar
Discovery of flavonoid derivatives as anti-HCV agents via pharmacophore search combining molecular docking strategy.
2012 Jun
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Jun 26 06:16:23 UTC 2021
Edited
by admin
on Sat Jun 26 06:16:23 UTC 2021
Record UNII
8O1CR18L82
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HYPEROSIDE
USP-RS  
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)
Created by admin on Sat Jun 26 06:16:23 UTC 2021 , Edited by admin on Sat Jun 26 06:16:23 UTC 2021
DSLD 4101 (Number of products:1)
Created by admin on Sat Jun 26 06:16:23 UTC 2021 , Edited by admin on Sat Jun 26 06:16:23 UTC 2021
Code System Code Type Description
USP_CATALOG
1335202
Created by admin on Sat Jun 26 06:16:23 UTC 2021 , Edited by admin on Sat Jun 26 06:16:23 UTC 2021
PRIMARY USP-RS
FDA UNII
8O1CR18L82
Created by admin on Sat Jun 26 06:16:23 UTC 2021 , Edited by admin on Sat Jun 26 06:16:23 UTC 2021
PRIMARY
PUBCHEM
5281643
Created by admin on Sat Jun 26 06:16:23 UTC 2021 , Edited by admin on Sat Jun 26 06:16:23 UTC 2021
PRIMARY
ECHA (EC/EINECS)
207-580-6
Created by admin on Sat Jun 26 06:16:23 UTC 2021 , Edited by admin on Sat Jun 26 06:16:23 UTC 2021
PRIMARY
CAS
482-36-0
Created by admin on Sat Jun 26 06:16:23 UTC 2021 , Edited by admin on Sat Jun 26 06:16:23 UTC 2021
PRIMARY
MESH
C021304
Created by admin on Sat Jun 26 06:16:23 UTC 2021 , Edited by admin on Sat Jun 26 06:16:23 UTC 2021
PRIMARY
WIKIPEDIA
HYPEROSIDE
Created by admin on Sat Jun 26 06:16:23 UTC 2021 , Edited by admin on Sat Jun 26 06:16:23 UTC 2021
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
USP
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
PARENT -> CONSTITUENT ALWAYS PRESENT
Secondary metabolite detected in developing cacao seeds.