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> Main
CHEBI:29608 - isoformononetin
Main
ChEBI Ontology
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ChEBI Name
isoformononetin
ChEBI ID
CHEBI:29608
Definition
A methoxyisoflavone that is isoflavone substituted at positions 4' and 7 by hydroxy and methoxy groups respectively.
Stars
This entity has been manually annotated by the ChEBI Team.
Submitter
Anonymous
Secondary ChEBI IDs
CHEBI:74940
Supplier Information
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Formula
C16H12O4
Net Charge
0
Average Mass
268.26410
Monoisotopic Mass
268.07356
InChI
InChI=1S/C16H12O4/c1-19-12-6-7-13-15(8-12)20-9-14(16(13)18)10-2-4-11(17)5-3-10/h2-9,17H,1H3
InChIKey
LNIQZRIHAMVRJA-UHFFFAOYSA-N
SMILES
COc1ccc2c(c1)occ(-c1ccc(O)cc1)c2=O
Roles Classification
Biological Role
(s):
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
apoptosis inhibitor
Any substance that inhibits the process of apoptosis (programmed cell death) in multi-celled organisms.
Application
(s):
bone density conservation agent
An agent that inhibits bone resorption and/or favor bone mineralization and bone regeneration. Used to heal bone fractures and to treat bone diseases such as osteopenia and osteoporosis.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
isoformononetin (
CHEBI:29608
)
has functional parent
daidzein (
CHEBI:28197
)
isoformononetin (
CHEBI:29608
)
has role
apoptosis inhibitor (
CHEBI:68494
)
isoformononetin (
CHEBI:29608
)
has role
bone density conservation agent (
CHEBI:50646
)
isoformononetin (
CHEBI:29608
)
has role
metabolite (
CHEBI:25212
)
isoformononetin (
CHEBI:29608
)
is a
7-methoxyisoflavones (
CHEBI:140356
)
isoformononetin (
CHEBI:29608
)
is a
hydroxyisoflavone (
CHEBI:38755
)
IUPAC Name
3-(4-hydroxyphenyl)-7-methoxy-4
H
-chromen-4-one
Synonyms
Sources
4'-Hydroxy-7-methoxyisoflavone
HMDB
4'-Hydroxy-7-methoxyisoflavone
KEGG COMPOUND
7-
O
-methyldaidzein
ChEBI
Manual Xrefs
Databases
C00009382
KNApSAcK
C12125
KEGG COMPOUND
CPD-3343
MetaCyc
DB04202
DrugBank
HMDB0033994
HMDB
HMO
PDBeChem
LMPK12050039
LIPID MAPS
View more database links
Registry Numbers
Types
Sources
251318
Reaxys Registry Number
Reaxys
486-63-5
CAS Registry Number
HMDB
Citations
Types
Sources
11006341
PubMed citation
Europe PMC
11129614
PubMed citation
Europe PMC
15896369
PubMed citation
Europe PMC
17707445
PubMed citation
Europe PMC
19598169
PubMed citation
Europe PMC
20395887
PubMed citation
Europe PMC
23395215
PubMed citation
Europe PMC
Last Modified
02 April 2018