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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H14O6
Molecular Weight 302.2788
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HOMOERIODICTYOL

SMILES

[H][C@]1(CC(=O)C2=C(O1)C=C(O)C=C2O)C3=CC=C(O)C(OC)=C3

InChI

InChIKey=FTODBIPDTXRIGS-ZDUSSCGKSA-N
InChI=1S/C16H14O6/c1-21-14-4-8(2-3-10(14)18)13-7-12(20)16-11(19)5-9(17)6-15(16)22-13/h2-6,13,17-19H,7H2,1H3/t13-/m0/s1

HIDE SMILES / InChI

Molecular Formula C16H14O6
Molecular Weight 302.2788
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Differential inhibitory effects of various flavonoids on the activities of reverse transcriptase and cellular DNA and RNA polymerases.
1990 Jul 5
Phenolic glycosides from Viscum angulatum.
2002 May
Separation of some chiral flavanones by micellar electrokinetic chromatography.
2003 Aug
Evaluation of bitter masking flavanones from Herba Santa (Eriodictyon californicum (H. and A.) Torr., Hydrophyllaceae).
2005 Jul 27
[Chemical constituents from Viscum nudum and their accelerating PC12 cell differentiation].
2006 Aug
Difference in plasma metabolite concentration after ingestion of lemon flavonoids and their aglycones in humans.
2006 Feb
Stereoisomeric separation of flavanones and flavanone-7-O-glycosides by capillary electrophoresis and determination of interconversion barriers.
2006 May 15
New bitter-masking compounds: hydroxylated benzoic acid amides of aromatic amines as structural analogues of homoeriodictyol.
2006 Nov 1
Enantioseparation of some chiral flavanones using microbial cyclic beta-(1-->3),(1-->6)-glucans as novel chiral additives in capillary electrophoresis.
2007 Apr 9
Simultaneous determination of homoeriodictyol-7-O-beta-D-Glccopyranoside and its metabolite homoeriodictyol in rat tissues and urine by liquid chromatography-mass spectrometry.
2007 May 9
Stereospecific high-performance liquid chromatographic validation of homoeriodictyol in serum and Yerba Santa (Eriodictyon glutinosum).
2008 Apr 14
Structural analogues of homoeriodictyol as flavor modifiers. Part III: short chain gingerdione derivatives.
2008 Aug 13
[Flavones from flowers of Paulownia fortunei].
2008 Nov
Lemon Polyphenols Suppress Diet-induced Obesity by Up-Regulation of mRNA Levels of the Enzymes Involved in beta-Oxidation in Mouse White Adipose Tissue.
2008 Nov
Enantiomeric separation of some flavanones using shinorhizobial linear octasaccharides in CE.
2008 Nov
Flavonoids from Bauhinia glauca subsp. pernervosa.
2009 Jun
Identification of bisprenylated benzoic acid derivatives from yerba santa (Eriodictyon ssp.) using sensory-guided fractionation.
2010 Feb 10
Characterization of flavor modulating effects in complex mixtures via high temperature liquid chromatography.
2010 Jan 13
Effects of Various Flavonoids on the α-Synuclein Fibrillation Process.
2010 Jan 28
[Studies on the flavonoids from Lignum Dalbergiae Odoriferae (II)].
2010 Jun
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:38:41 GMT 2023
Edited
by admin
on Fri Dec 15 18:38:41 GMT 2023
Record UNII
EHE7H3705C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HOMOERIODICTYOL
MI  
Common Name English
HOMOERIODICTYOL [MI]
Common Name English
(-)-HOMOERIODICTYOL
Common Name English
ERIODICTYONONE
Common Name English
(S)-2,3-DIHYDRO-5,7-DIHYDROXY-2-(4-HYDROXY-3-METHOXYPHENYL)-4-BENZOPYRONE
Systematic Name English
5,7,4'-TRIHYDROXY-3'-METHOXYFLAVANONE
Systematic Name English
Code System Code Type Description
MESH
C503231
Created by admin on Fri Dec 15 18:38:41 GMT 2023 , Edited by admin on Fri Dec 15 18:38:41 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-173-3
Created by admin on Fri Dec 15 18:38:41 GMT 2023 , Edited by admin on Fri Dec 15 18:38:41 GMT 2023
PRIMARY
CHEBI
74960
Created by admin on Fri Dec 15 18:38:41 GMT 2023 , Edited by admin on Fri Dec 15 18:38:41 GMT 2023
PRIMARY
WIKIPEDIA
HOMOERIODICTYOL
Created by admin on Fri Dec 15 18:38:41 GMT 2023 , Edited by admin on Fri Dec 15 18:38:41 GMT 2023
PRIMARY
EPA CompTox
DTXSID30196243
Created by admin on Fri Dec 15 18:38:41 GMT 2023 , Edited by admin on Fri Dec 15 18:38:41 GMT 2023
PRIMARY
PUBCHEM
73635
Created by admin on Fri Dec 15 18:38:41 GMT 2023 , Edited by admin on Fri Dec 15 18:38:41 GMT 2023
PRIMARY
CAS
446-71-9
Created by admin on Fri Dec 15 18:38:41 GMT 2023 , Edited by admin on Fri Dec 15 18:38:41 GMT 2023
PRIMARY
MERCK INDEX
m6044
Created by admin on Fri Dec 15 18:38:41 GMT 2023 , Edited by admin on Fri Dec 15 18:38:41 GMT 2023
PRIMARY Merck Index
FDA UNII
EHE7H3705C
Created by admin on Fri Dec 15 18:38:41 GMT 2023 , Edited by admin on Fri Dec 15 18:38:41 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY