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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

COC1=CC(=CC=C1O)[C@@H]2CC(=O)C3=C(O2)C=C(O)C=C3O

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
[Studies on the flavonoids from Lignum Dalbergiae Odoriferae (II)].
2010-06
Identification of bisprenylated benzoic acid derivatives from yerba santa (Eriodictyon ssp.) using sensory-guided fractionation.
2010-02-10
Effects of Various Flavonoids on the α-Synuclein Fibrillation Process.
2010-01-28
Characterization of flavor modulating effects in complex mixtures via high temperature liquid chromatography.
2010-01-13
Flavonoids from Bauhinia glauca subsp. pernervosa.
2009-06
[Flavones from flowers of Paulownia fortunei].
2008-11
Lemon Polyphenols Suppress Diet-induced Obesity by Up-Regulation of mRNA Levels of the Enzymes Involved in beta-Oxidation in Mouse White Adipose Tissue.
2008-11
Enantiomeric separation of some flavanones using shinorhizobial linear octasaccharides in CE.
2008-11
Structural analogues of homoeriodictyol as flavor modifiers. Part III: short chain gingerdione derivatives.
2008-08-13
Stereospecific high-performance liquid chromatographic validation of homoeriodictyol in serum and Yerba Santa (Eriodictyon glutinosum).
2008-04-14
Simultaneous determination of homoeriodictyol-7-O-beta-D-Glccopyranoside and its metabolite homoeriodictyol in rat tissues and urine by liquid chromatography-mass spectrometry.
2007-05-09
Enantioseparation of some chiral flavanones using microbial cyclic beta-(1-->3),(1-->6)-glucans as novel chiral additives in capillary electrophoresis.
2007-04-09
New bitter-masking compounds: hydroxylated benzoic acid amides of aromatic amines as structural analogues of homoeriodictyol.
2006-11-01
[Chemical constituents from Viscum nudum and their accelerating PC12 cell differentiation].
2006-08
Stereoisomeric separation of flavanones and flavanone-7-O-glycosides by capillary electrophoresis and determination of interconversion barriers.
2006-05-15
Difference in plasma metabolite concentration after ingestion of lemon flavonoids and their aglycones in humans.
2006-02
Evaluation of bitter masking flavanones from Herba Santa (Eriodictyon californicum (H. and A.) Torr., Hydrophyllaceae).
2005-07-27
Identification and quantification of the conjugated metabolites derived from orally administered hesperidin in rat plasma.
2004-10-20
Effect of the rootstock and interstock grafted in lemon tree (Citrus limon (L.) Burm.) on the flavonoid content of lemon juice.
2004-01-28
Separation of some chiral flavanones by micellar electrokinetic chromatography.
2003-08
O-demethylation and sulfation of 7-methoxylated flavanones by Cunninghamella elegans.
2003-02
Phenolic glycosides from Viscum angulatum.
2002-05
Differential inhibitory effects of various flavonoids on the activities of reverse transcriptase and cellular DNA and RNA polymerases.
1990-07-05
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:17:51 GMT 2025
Edited
by admin
on Mon Mar 31 19:17:51 GMT 2025
Record UNII
EHE7H3705C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HOMOERIODICTYOL [MI]
Preferred 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 Mon Mar 31 19:17:51 GMT 2025 , Edited by admin on Mon Mar 31 19:17:51 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-173-3
Created by admin on Mon Mar 31 19:17:51 GMT 2025 , Edited by admin on Mon Mar 31 19:17:51 GMT 2025
PRIMARY
CHEBI
74960
Created by admin on Mon Mar 31 19:17:51 GMT 2025 , Edited by admin on Mon Mar 31 19:17:51 GMT 2025
PRIMARY
WIKIPEDIA
HOMOERIODICTYOL
Created by admin on Mon Mar 31 19:17:51 GMT 2025 , Edited by admin on Mon Mar 31 19:17:51 GMT 2025
PRIMARY
EPA CompTox
DTXSID30196243
Created by admin on Mon Mar 31 19:17:51 GMT 2025 , Edited by admin on Mon Mar 31 19:17:51 GMT 2025
PRIMARY
PUBCHEM
73635
Created by admin on Mon Mar 31 19:17:51 GMT 2025 , Edited by admin on Mon Mar 31 19:17:51 GMT 2025
PRIMARY
CAS
446-71-9
Created by admin on Mon Mar 31 19:17:51 GMT 2025 , Edited by admin on Mon Mar 31 19:17:51 GMT 2025
PRIMARY
MERCK INDEX
m6044
Created by admin on Mon Mar 31 19:17:51 GMT 2025 , Edited by admin on Mon Mar 31 19:17:51 GMT 2025
PRIMARY Merck Index
FDA UNII
EHE7H3705C
Created by admin on Mon Mar 31 19:17:51 GMT 2025 , Edited by admin on Mon Mar 31 19:17:51 GMT 2025
PRIMARY
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