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 ChemicalBook:CB4480952, eMolecules:1935781, ZINC000000519621
Download Molfile XML SDF
Formulae C16H12O6
C16H12O6
Net Charge 0
Average Mass 300.26290
Monoisotopic Mass 300.06339
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)
velutin (CHEBI:177047) 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
491-71-4 CAS Registry Number ChemIDplus
Citations
Last Modified
19 July 2022