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CHEBI:16400 - gossypetin

ChEBI IDCHEBI:16400
ChEBI Namegossypetin
Stars
DefinitionA hexahydroxyflavone having the hydroxy groups placed at the 3-, 3'-, 4'-, 5- 7- and 8-positions.
Secondary ChEBI IDsCHEBI:1362, CHEBI:11682, CHEBI:19860, CHEBI:38341
Last Modified26 February 2016
SubmitterMarcus Ennis
DownloadsMolfile
FormulaC15H10O8
Net Charge0
Average Mass318.237
Monoisotopic Mass318.03757
SMILESO=c1c(O)c(-c2ccc(O)c(O)c2)oc2c(O)c(O)cc(O)c12
InChIInChI=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
InChIKeyYRRAGUMVDQQZIY-UHFFFAOYSA-N
Wikipedia
Roles Classification
Biological Role:
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
ChEBI Ontology
Outgoing Relation(s)
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-3-olate (CHEBI:57759)
gossypetin (CHEBI:16400) is conjugate acid of gossypetin(1−) (CHEBI:77862)
Incoming Relation(s)
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-3-olate (CHEBI:57759) is conjugate base of gossypetin (CHEBI:16400)
gossypetin(1−) (CHEBI:77862) is conjugate base of gossypetin (CHEBI:16400)
IUPAC Name 
2-(3,4-dihydroxyphenyl)-3,5,7,8-tetrahydroxy-4H-chromen-4-one
Synonyms  Source
3,3',4',5,7,8-HexahydroxyflavoneKEGG COMPOUND
ArticulatidinChemIDplus
EquisporolChEBI
GossypetinKEGG COMPOUND
Manual XrefsDatabases
C04109KEGG COMPOUND
GossypetinWikipedia
334578-HEXAHYDROXYFLAVONEMetaCyc
LMPK12113231LIPID MAPS
WO0103681Patent
JP55054883Patent
C00004721KNApSAcK
LSM-36971LINCS
Registry NumbersSources
Reaxys:332194Reaxys
CAS:489-35-0ChemIDplus
Citations