CHEBI:16514 - 4',5,7-trihydroxy-3'-methoxyflavone

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name 4',5,7-trihydroxy-3'-methoxyflavone
ChEBI ID CHEBI:16514
Definition The 3'-O-methyl derivative of luteolin.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:12083, CHEBI:2006, CHEBI:20519
Supplier Information
Download Molfile XML SDF
Formulae C16H12O6
C16H12O6
Net Charge 0
Average Mass 300.26290
Monoisotopic Mass 300.063
InChI InChI=1S/C16H12O6/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/h2-7,17-19H,1H3
InChIKey SCZVLDHREVKTSH-UHFFFAOYSA-N
SMILES COc1cc(ccc1O)-c1cc(=O)c2c(O)cc(O)cc2o1
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514) has functional parent luteolin (CHEBI:15864)
4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514) has role antineoplastic agent (CHEBI:35610)
4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514) has role antioxidant (CHEBI:22586)
4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514) has role metabolite (CHEBI:25212)
4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514) is a monomethoxyflavone (CHEBI:25401)
4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514) is a trihydroxyflavone (CHEBI:27116)
4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514) is conjugate acid of 4',5-dihydroxy-3'-methoxyflavon-7-olate(1−) (CHEBI:57799)
Incoming 6-C-(α-L-arabinosyl)-8-C-(β-L-arabinosyl)chrysoeriol (CHEBI:131758) has functional parent 4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514)
7-O-(6-p-coumaroylglucosyl)chrysoeriol (CHEBI:75509) has functional parent 4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514)
7-O-[α-L-rhamnosyl-(1→2)-β-D-glucosyl]chrysoeriol (CHEBI:75523) has functional parent 4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514)
chrysoeriol 7-O-gentiobioside (CHEBI:75398) has functional parent 4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514)
geraldone (CHEBI:5326) has functional parent 4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514)
isoscoparin (CHEBI:18200) has functional parent 4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514)
4',5-dihydroxy-3'-methoxyflavon-7-olate(1−) (CHEBI:57799) is conjugate base of 4',5,7-trihydroxy-3'-methoxyflavone (CHEBI:16514)
IUPAC Name
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-chromen-4-one
Synonyms Sources
3'-Methoxyapigenin ChemIDplus
3'-O-Methylluteolin KEGG COMPOUND
5,7,4'-Trihydroxy-3'-methoxyflavone KEGG COMPOUND
5,7,4'-Trihydroxy-3'-methoxyflavone KEGG COMPOUND
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-benzopyrone ChEBI
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-1-benzopyran-4-one ChEBI
Chryseriol ChemIDplus
Chrysoeriol KEGG COMPOUND
Luteolin 3'-methyl ether ChemIDplus
Manual Xrefs Databases
574-TRIHYDROXY-3-METHOXYFLAVONE MetaCyc
C00001029 KNApSAcK
C04293 KEGG COMPOUND
LMPK12110799 LIPID MAPS
View more database links
Registry Numbers Types Sources
295004 Reaxys Registry Number Reaxys
295004 Beilstein Registry Number Beilstein
491-71-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
22438130 PubMed citation Europe PMC
22577954 PubMed citation Europe PMC
23017389 PubMed citation Europe PMC
23052184 PubMed citation Europe PMC
23122135 PubMed citation Europe PMC
Last Modified
17 November 2016