CHEBI:3421 - carlinoside

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ChEBI Name carlinoside
ChEBI ID CHEBI:3421
Definition A C-glycosyl compound that is luteolin substituted at positions 8 and 6 by α-L-arabinopyranosyl and β-D-glucosyl residues respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C26H28O15
Net Charge 0
Average Mass 580.49150
Monoisotopic Mass 580.14282
InChI InChI=1S/C26H28O15/c27-5-13-18(33)21(36)23(38)26(41-13)15-19(34)14-10(30)4-12(7-1-2-8(28)9(29)3-7)40-24(14)16(20(15)35)25-22(37)17(32)11(31)6-39-25/h1-4,11,13,17-18,21-23,25-29,31-38H,5-6H2/t11-,13+,17-,18+,21-,22+,23+,25-,26-/m0/s1
InChIKey XBGYTZHKGMCEGE-VYUBKLCTSA-N
SMILES OC[C@H]1O[C@H]([C@H](O)[C@@H](O)[C@@H]1O)c1c(O)c([C@@H]2OC[C@H](O)[C@H](O)[C@H]2O)c2oc(cc(=O)c2c1O)-c1ccc(O)c(O)c1
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application(s): anti-inflammatory agent
Any compound that has anti-inflammatory effects.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing carlinoside (CHEBI:3421) has functional parent luteolin (CHEBI:15864)
carlinoside (CHEBI:3421) has role anti-inflammatory agent (CHEBI:67079)
carlinoside (CHEBI:3421) has role antioxidant (CHEBI:22586)
carlinoside (CHEBI:3421) has role metabolite (CHEBI:25212)
carlinoside (CHEBI:3421) is a C-glycosyl compound (CHEBI:20857)
carlinoside (CHEBI:3421) is a tetrahydroxyflavone (CHEBI:38684)
Synonyms Sources
6-C-β-D-glucosyl-8-C-α-L-arabinopyranosylluteolin ChEBI
8-C-α-L-arabinopyranosyl-6-C-β-D-glucosylluteolin ChEBI
luteolin 6-C-β-D-glucopyranoside-8-C-α-L-arabinopyranoside LIPID MAPS
luteolin 6-C-glucoside-8-C-arabinoside ChEBI
Manual Xrefs Databases
C00006184 KNApSAcK
C10026 KEGG COMPOUND
LMPK12110488 LIPID MAPS
View more database links
Registry Numbers Types Sources
59952-97-5 CAS Registry Number KEGG COMPOUND
6563440 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
10820082 PubMed citation Europe PMC
17981413 PubMed citation Europe PMC
21801714 PubMed citation Europe PMC
905416 PubMed citation Europe PMC
Last Modified
28 July 2014