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CHEBI:28436 - delphinidin

Default Structure
ChEBI IDCHEBI:28436
ChEBI Namedelphinidin
Stars
DefinitionAn anthocyanidin cation consisting of benzopyrylium with hydroxy substituents at the 3-, 5- and 7-positions and a 3,4,5-trihydroxyphenyl group at the 2-position. It is a plant pigment responsible for the colours of the plants of the genera Viola and Delphinium.
Secondary ChEBI IDsCHEBI:4382, CHEBI:23600
Last Modified16 December 2019
DownloadsMolfile
FormulaC15H11O7
Net Charge+1
Average Mass303.246
Monoisotopic Mass303.04993
SMILESOc1cc(O)c2cc(O)c(-c3cc(O)c(O)c(O)c3)[o+]c2c1
InChIInChI=1S/C15H10O7/c16-7-3-9(17)8-5-12(20)15(22-13(8)4-7)6-1-10(18)14(21)11(19)2-6/h1-5H,(H5-,16,17,18,19,20,21)/p+1
InChIKeyJKHRCGUTYDNCLE-UHFFFAOYSA-O
Wikipedia
Roles Classification
Biological Roles:
biological pigment  An endogenous molecular entity that results in a colour of an organism as the consequence of the selective absorption of light.
plant metabolite  Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application:
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
ChEBI Ontology
Outgoing Relation(s)
delphinidin (CHEBI:28436) has role antineoplastic agent (CHEBI:35610)
delphinidin (CHEBI:28436) has role biological pigment (CHEBI:26130)
delphinidin (CHEBI:28436) has role plant metabolite (CHEBI:76924)
delphinidin (CHEBI:28436) is a 5-hydroxyanthocyanidin (CHEBI:140277)
delphinidin (CHEBI:28436) is conjugate acid of delphinidin(1−) (CHEBI:144775)
Incoming Relation(s)
delphinidin 3-O-(6-O-(E)-4-coumaroyl-β-D-glucoside) (CHEBI:75677) has functional parent delphinidin (CHEBI:28436)
delphinidin 3-O-(6-O-(Z)-4-coumaroyl-β-D-glucoside) (CHEBI:75675) has functional parent delphinidin (CHEBI:28436)
delphinidin 3-O-(6-O-acetyl-β-D-glucoside) (CHEBI:75678) has functional parent delphinidin (CHEBI:28436)
delphinidin 3-O-(6''-O-malonyl)-β-D-glucoside (CHEBI:55334) has functional parent delphinidin (CHEBI:28436)
delphinidin 3-O-(6''-O-malonyl)-β-D-glucoside-3'-O-β-D-glucoside (CHEBI:55336) has functional parent delphinidin (CHEBI:28436)
delphinidin 3-O-rutinoside-7-O-β-D-glucoside (CHEBI:145693) has functional parent delphinidin (CHEBI:28436)
delphinidin 3-O-β-D-glucoside (CHEBI:31463) has functional parent delphinidin (CHEBI:28436)
delphinidin 3-O-β-D-glucoside-5-O-β-D-glucoside (CHEBI:55455) has functional parent delphinidin (CHEBI:28436)
delphinidin 3-O-β-D-sambubioside (CHEBI:74810) has functional parent delphinidin (CHEBI:28436)
delphinidin 3,3',5-tri-O-glucoside (CHEBI:55456) has functional parent delphinidin (CHEBI:28436)
malvidin (CHEBI:6674) has functional parent delphinidin (CHEBI:28436)
ternatin C5 (CHEBI:55335) has functional parent delphinidin (CHEBI:28436)
delphinidin chloride (CHEBI:38701) has part delphinidin (CHEBI:28436)
delphinidin(1−) (CHEBI:144775) is conjugate base of delphinidin (CHEBI:28436)
IUPAC Name 
3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromenium
Synonym  Source
3,3',4',5,5',7-HexahydroxyflavyliumChemIDplus
Manual XrefsDatabases
C00020091KNApSAcK
C05908KEGG COMPOUND
DelphinidinWikipedia
LMPK12010001LIPID MAPS
Registry NumbersSources
Reaxys:1691007Reaxys
CAS:13270-61-6ChemIDplus
Citations