CHEBI:75164 - patuletin

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name patuletin
ChEBI ID CHEBI:75164
Definition A trimethoxyflavone that is quercetagetin methylated at position 6.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Anonymous
Secondary ChEBI IDs CHEBI:7942
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Formula C16H12O8
Net Charge 0
Average Mass 332.26170
Monoisotopic Mass 332.053
InChI InChI=1S/C16H12O8/c1-23-16-9(19)5-10-11(13(16)21)12(20)14(22)15(24-10)6-2-3-7(17)8(18)4-6/h2-5,17-19,21-22H,1H3
InChIKey JMIFIYIEXODVTO-UHFFFAOYSA-N
SMILES COc1c(O)cc2oc(-c3ccc(O)c(O)c3)c(O)c(=O)c2c1O
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): analgesic
An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
EC 1.1.1.21 (aldehyde reductase) inhibitor
An EC 1.1.1.* (oxidoreductase acting on donor CH-OH group, NAD+ or NADP+ acceptor) inhibitor that interferes with the action of aldehyde reductase (EC 1.1.1.21).
lipoxygenase inhibitor
A compound or agent that combines with lipoxygenase and thereby prevents its substrate-enzyme combination with arachidonic acid and the formation of the icosanoid products hydroxyicosatetraenoic acid and various leukotrienes.
Application(s): analgesic
An agent capable of relieving pain without the loss of consciousness or without producing anaesthesia. In addition, analgesic is a role played by a compound which is exhibited by a capability to cause a reduction of pain symptoms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing patuletin (CHEBI:75164) has functional parent quercetagetin (CHEBI:8695)
patuletin (CHEBI:75164) has role analgesic (CHEBI:35480)
patuletin (CHEBI:75164) has role antioxidant (CHEBI:22586)
patuletin (CHEBI:75164) has role EC 1.1.1.21 (aldehyde reductase) inhibitor (CHEBI:48550)
patuletin (CHEBI:75164) has role lipoxygenase inhibitor (CHEBI:35856)
patuletin (CHEBI:75164) has role metabolite (CHEBI:25212)
patuletin (CHEBI:75164) is a flavonols (CHEBI:28802)
patuletin (CHEBI:75164) is a monomethoxyflavone (CHEBI:25401)
patuletin (CHEBI:75164) is a pentahydroxyflavone (CHEBI:25883)
IUPAC Name
2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-methoxy-4H-chromen-4-one
Synonyms Sources
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-6-methoxy-4-benzopyrone ChemIDplus
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-6-methoxy-4H-1-benzopyran-4-one HMDB
3',4',5,7-Tetrahydroxy-6-methoxyflavonol HMDB
3,5,7,3',4'-Pentahydroxy-6-methoxyflavone LIPID MAPS
6-Methoxyquercetin LIPID MAPS
6-O-Methylquercetagetin HMDB
Quercetagetin 6-methyl ether KEGG COMPOUND
Manual Xrefs Databases
C00004680 KNApSAcK
C10118 KEGG COMPOUND
CPD-14907 MetaCyc
HMDB0030802 HMDB
LMPK12112986 LIPID MAPS
Patuletin Wikipedia
US5858371 Patent
View more database links
Registry Numbers Types Sources
335897 Reaxys Registry Number Reaxys
519-96-0 CAS Registry Number KEGG COMPOUND
519-96-0 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10650074 PubMed citation Europe PMC
11909694 PubMed citation Europe PMC
1843126 PubMed citation Europe PMC
18998399 PubMed citation Europe PMC
21284510 PubMed citation Europe PMC
21500799 PubMed citation Europe PMC
23196154 PubMed citation Europe PMC
Last Modified
28 July 2014