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CHEBI:66046 - 6-hydroxyluteolin 7-O-laminaribioside

ChEBI IDCHEBI:66046
ChEBI Name6-hydroxyluteolin 7-O-laminaribioside
Stars
ASCII Name6-hydroxyluteolin 7-O-laminaribioside
DefinitionA glycosyloxyflavone that is 6-hydroxyluteolin attached to a β-D-glucopyranosyl-(1→3)-β-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. Isolated from Globularia cordifolia and Globularia alypum, it exhibits antioxidant activity.
Last Modified26 February 2013
DownloadsMolfile
FormulaC27H30O17
Net Charge0
Average Mass626.520
Monoisotopic Mass626.14830
SMILES[H][C@]1(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@@H](CO)O[C@@H](Oc2cc3oc(-c4ccc(O)c(O)c4)cc(=O)c3c(O)c2O)[C@@H]1O
InChIInChI=1S/C27H30O17/c28-6-15-19(34)22(37)23(38)26(42-15)44-25-20(35)16(7-29)43-27(24(25)39)41-14-5-13-17(21(36)18(14)33)11(32)4-12(40-13)8-1-2-9(30)10(31)3-8/h1-5,15-16,19-20,22-31,33-39H,6-7H2/t15-,16-,19-,20-,22+,23-,24-,25+,26+,27-/m1/s1
InChIKeyYNOSNIYDHUBEBU-HGKFCXGKSA-N
Species of MetaboliteComponentSourceComments
Globularia alypum (IPNI:813050-1) aerial part (BTO:0001658) PubMed (16124783)
Globularia cordifolia (ncbitaxon:69063) leaf (BTO:0000713) PubMed (16124783)
Roles Classification
Chemical Role:
antioxidant  A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role:
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
ChEBI Ontology
Outgoing Relation(s)
6-hydroxyluteolin 7-O-laminaribioside (CHEBI:66046) has functional parent luteolin (CHEBI:15864)
6-hydroxyluteolin 7-O-laminaribioside (CHEBI:66046) has role antioxidant (CHEBI:22586)
6-hydroxyluteolin 7-O-laminaribioside (CHEBI:66046) has role metabolite (CHEBI:25212)
6-hydroxyluteolin 7-O-laminaribioside (CHEBI:66046) is a disaccharide derivative (CHEBI:63353)
6-hydroxyluteolin 7-O-laminaribioside (CHEBI:66046) is a glycosyloxyflavone (CHEBI:50018)
6-hydroxyluteolin 7-O-laminaribioside (CHEBI:66046) is a tetrahydroxyflavone (CHEBI:38684)
IUPAC Name 
2-(3,4-dihydroxyphenyl)-5,6-dihydroxy-4-oxo-4H-chromen-7-yl 3-O-β-D-glucopyranosyl-β-D-glucopyranoside
Synonym  Source
5,6,3',4'-tetrahydroxyflavone-7-O-β-D-glucopyranosyl-(1→3)-β-D-glucopyranosideChEBI
Registry NumbersSources
Reaxys:15769702Reaxys
Citations