CHEBI:7602 - nobiletin

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ChEBI Name nobiletin
ChEBI ID CHEBI:7602
Definition A methoxyflavone that is flavone substituted by methoxy groups at positions 5, 6, 7, 8, 3' and 4' respectively.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C21H22O8
Net Charge 0
Average Mass 402.39460
Monoisotopic Mass 402.13147
InChI InChI=1S/C21H22O8/c1-23-13-8-7-11(9-15(13)24-2)14-10-12(22)16-17(25-3)19(26-4)21(28-6)20(27-5)18(16)29-14/h7-10H,1-6H3
InChIKey MRIAQLRQZPPODS-UHFFFAOYSA-N
SMILES COc1ccc(cc1OC)-c1cc(=O)c2c(OC)c(OC)c(OC)c(OC)c2o1
Roles Classification
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
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ChEBI Ontology
Outgoing nobiletin (CHEBI:7602) has functional parent flavone (CHEBI:42491)
nobiletin (CHEBI:7602) has role antineoplastic agent (CHEBI:35610)
nobiletin (CHEBI:7602) has role plant metabolite (CHEBI:76924)
nobiletin (CHEBI:7602) is a methoxyflavone (CHEBI:25241)
IUPAC Name
2-(3,4-dimethoxyphenyl)-5,6,7,8-tetramethoxy-4H-1-benzopyran-4-one
Synonyms Sources
5,6,7,8,3',4'-Hexamethoxyflavone KEGG COMPOUND
Hexamethoxyflavone KEGG COMPOUND
Manual Xrefs Databases
C00001076 KNApSAcK
C10112 KEGG COMPOUND
HMDB0029540 HMDB
LMPK12111468 LIPID MAPS
LSM-2130 LINCS
Nobiletin Wikipedia
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Registry Numbers Types Sources
360887 Reaxys Registry Number Reaxys
478-01-3 CAS Registry Number ChemIDplus
478-01-3 CAS Registry Number NIST Chemistry WebBook
Citations Waiting for Citations Types Sources
25488359 PubMed citation Europe PMC
25845666 PubMed citation Europe PMC
Last Modified
24 February 2016