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CHEBI:65569 - camellianoside

ChEBI IDCHEBI:65569
ChEBI Namecamellianoside
Stars
DefinitionA quercetin O-glucoside consisting of quercetin having a β-D-xylopyranosyl-(1→3)-6-deoxy-α-L-mannopyranosyl-(1→6)-β-D-glucopyranosyl residue at position 3. It is isolated from the leaves of Camellia japonica and exhibits antioxidant activity.
Last Modified4 December 2012
DownloadsMolfile
FormulaC32H38O20
Net Charge0
Average Mass742.636
Monoisotopic Mass742.19564
SMILES[H][C@@]1(O[C@@H]2[C@@H](O)[C@H](C)O[C@@H](OC[C@H]3O[C@@H](Oc4c(-c5ccc(O)c(O)c5)oc5cc(O)cc(O)c5c4=O)[C@H](O)[C@@H](O)[C@@H]3O)[C@@H]2O)OC[C@@H](O)[C@H](O)[C@H]1O
InChIInChI=1S/C32H38O20/c1-9-19(38)28(51-30-24(43)20(39)15(37)7-46-30)26(45)31(48-9)47-8-17-21(40)23(42)25(44)32(50-17)52-29-22(41)18-14(36)5-11(33)6-16(18)49-27(29)10-2-3-12(34)13(35)4-10/h2-6,9,15,17,19-21,23-26,28,30-40,42-45H,7-8H2,1H3/t9-,15+,17+,19-,20-,21+,23-,24+,25+,26+,28+,30-,31+,32-/m0/s1
InChIKeyGSTBDLJYXUQTFK-FODKTCEYSA-N
Species of MetaboliteComponentSourceComments
Camellia japonica (ncbitaxon:4443) leaf (BTO:0000713) PubMed (16926516) Fresh leaves
Roles Classification
Chemical Role:
radical scavenger  A role played by a substance that can react readily with, and thereby eliminate, radicals.
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)
camellianoside (CHEBI:65569) has role metabolite (CHEBI:25212)
camellianoside (CHEBI:65569) has role radical scavenger (CHEBI:48578)
camellianoside (CHEBI:65569) is a quercetin O-glucoside (CHEBI:64621)
camellianoside (CHEBI:65569) is a trisaccharide derivative (CHEBI:63571)
camellianoside (CHEBI:65569) is a β-D-glucoside (CHEBI:22798)
IUPAC Name 
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl β-D-xylopyranosyl-(1→3)-6-deoxy-α-L-mannopyranosyl-(1→6)-β-D-glucopyranoside
Synonym  Source
quercetin 3-O-β-xylopyranosyl-(1→3)-O-α-L-rhamnopyranosyl-(1→6)-O-β-D-glucopyranosideChEBI
Registry NumbersSources
Reaxys:11115000Reaxys
Citations