CHEBI:81093 - kurarinol

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name kurarinol
Definition A trihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 7, 2' and 4' , a methoxy group at position 5 and a (2S)-5-hydroxy-5-methyl-2-(prop-1-en-2-yl)hexyl group at position 8 respectively.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C26H32O7
Net Charge 0
Average Mass 456.52810
Monoisotopic Mass 456.21480
InChI InChI=1S/C26H32O7/c1-14(2)15(8-9-26(3,4)31)10-18-20(29)12-23(32-5)24-21(30)13-22(33-25(18)24)17-7-6-16(27)11-19(17)28/h6-7,11-12,15,22,27-29,31H,1,8-10,13H2,2-5H3/t15-,22+/m1/s1
SMILES COc1cc(O)c(C[C@@H](CCC(C)(C)O)C(C)=C)c2O[C@@H](CC(=O)c12)c1ccc(O)cc1O
Metabolite of Species Details
Sophora flavescens (NCBI:txid49840) Found in root (BTO:0001188). See: PubMed
Roles Classification
Chemical Role(s): antioxidant
A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides.
Biological Role(s): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
Application(s): anti-inflammatory agent
Any compound that has anti-inflammatory effects.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing kurarinol (CHEBI:81093) has functional parent (2S)-flavanone (CHEBI:15606)
kurarinol (CHEBI:81093) has role anti-inflammatory agent (CHEBI:67079)
kurarinol (CHEBI:81093) has role antioxidant (CHEBI:22586)
kurarinol (CHEBI:81093) has role plant metabolite (CHEBI:76924)
kurarinol (CHEBI:81093) is a 4'-hydroxyflavanones (CHEBI:140331)
kurarinol (CHEBI:81093) is a monomethoxyflavanone (CHEBI:38738)
kurarinol (CHEBI:81093) is a trihydroxyflavanone (CHEBI:38739)
Manual Xrefs Databases
C00019183 KNApSAcK
View more database links
Registry Numbers Types Sources
19204008 Reaxys Registry Number Reaxys
855746-98-4 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
17951038 PubMed citation Europe PMC
18451517 PubMed citation Europe PMC
24997323 PubMed citation Europe PMC
Last Modified
05 April 2018