CHEBI:16400 - gossypetin

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ChEBI Name gossypetin
ChEBI ID CHEBI:16400
Definition A hexahydroxyflavone having the hydroxy groups placed at the 3-, 3'-, 4'-, 5- 7- and 8-positions.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:38341, CHEBI:19860, CHEBI:11682, CHEBI:1362
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Formulae C15H10O8
C15H10O8
Net Charge 0
Average Mass 318.23510
Monoisotopic Mass 318.03757
InChI InChI=1S/C15H10O8/c16-6-2-1-5(3-7(6)17)14-13(22)12(21)10-8(18)4-9(19)11(20)15(10)23-14/h1-4,16-20,22H
InChIKey YRRAGUMVDQQZIY-UHFFFAOYSA-N
SMILES Oc1ccc(cc1O)-c1oc2c(O)c(O)cc(O)c2c(=O)c1O
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.
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ChEBI Ontology
Outgoing gossypetin (CHEBI:16400) has role plant metabolite (CHEBI:76924)
gossypetin (CHEBI:16400) is a 7-hydroxyflavonol (CHEBI:52267)
gossypetin (CHEBI:16400) is a hexahydroxyflavone (CHEBI:24561)
gossypetin (CHEBI:16400) is conjugate acid of gossypetin(1−) (CHEBI:77862)
gossypetin (CHEBI:16400) is conjugate acid of gossypetin-3-olate (CHEBI:57759)
Incoming 2,3-dihydrogossypetin (CHEBI:16965) has functional parent gossypetin (CHEBI:16400)
3,3',4',5,7-pentahydroxy-8-methoxyflavone (CHEBI:28018) has functional parent gossypetin (CHEBI:16400)
gossypetin 8-rhamnoside (CHEBI:28086) has functional parent gossypetin (CHEBI:16400)
gossypin (CHEBI:5525) has functional parent gossypetin (CHEBI:16400)
gossypetin(1−) (CHEBI:77862) is conjugate base of gossypetin (CHEBI:16400)
gossypetin-3-olate (CHEBI:57759) is conjugate base of gossypetin (CHEBI:16400)
IUPAC Name
2-(3,4-dihydroxyphenyl)-3,5,7,8-tetrahydroxy-4H-chromen-4-one
Synonyms Sources
3,3',4',5,7,8-Hexahydroxyflavone KEGG COMPOUND
Articulatidin ChemIDplus
Equisporol ChEBI
Gossypetin KEGG COMPOUND
Manual Xrefs Databases
334578-HEXAHYDROXYFLAVONE MetaCyc
C00004721 KNApSAcK
C04109 KEGG COMPOUND
Gossypetin Wikipedia
JP55054883 Patent
LMPK12113231 LIPID MAPS
LSM-36971 LINCS
WO0103681 Patent
View more database links
Registry Numbers Types Sources
332194 Reaxys Registry Number Reaxys
332194 Beilstein Registry Number Beilstein
489-35-0 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
19895818 PubMed citation Europe PMC
22953867 PubMed citation Europe PMC
2676226 PubMed citation Europe PMC
8424824 PubMed citation Europe PMC
Last Modified
26 February 2016