CHEBI:69086 - glycyrin

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ChEBI Name glycyrin
Definition A member of the class of coumarins that is coumarin substituted by methoxy groups at positions 5 and 7, a prenyl group at position 6 and a 2,4-dihydroxyphenyl group at position 3. Isolated from Glycyrrhiza uralensis, it exhibits antibacterial activity.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C22H22O6
Net Charge 0
Average Mass 382.40650
Monoisotopic Mass 382.14164
InChI InChI=1S/C22H22O6/c1-12(2)5-7-15-19(26-3)11-20-17(21(15)27-4)10-16(22(25)28-20)14-8-6-13(23)9-18(14)24/h5-6,8-11,23-24H,7H2,1-4H3
SMILES COc1cc2oc(=O)c(cc2c(OC)c1CC=C(C)C)-c1ccc(O)cc1O
Metabolite of Species Details
Glycyrrhiza uralensis (NCBI:txid74613) Found in root (BTO:0001188). Dried and ground roots extracted with supercritical CO2 with 5% EtOH as modifier See: PubMed
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing glycyrin (CHEBI:69086) has role antibacterial agent (CHEBI:33282)
glycyrin (CHEBI:69086) has role metabolite (CHEBI:25212)
glycyrin (CHEBI:69086) has role plant metabolite (CHEBI:76924)
glycyrin (CHEBI:69086) is a aromatic ether (CHEBI:35618)
glycyrin (CHEBI:69086) is a coumarins (CHEBI:23403)
glycyrin (CHEBI:69086) is a hydroxyisoflavans (CHEBI:76250)
Synonyms Sources
3-(2ʼ,4ʼ-dihydroxyphenyl)-5,7-dimethoxy-2-isopentenylcoumarin ChEBI
3-(2,4-dihydroxyphenyl)-5,7-dimethoxy-6-(3-methyl-but-2-enyl)-1-benzopyran-2-one ChemIDplus
3-(2,4-dihydroxyphenyl)-5,7-dimethoxy-6-prenylcoumarin LIPID MAPS
Manual Xrefs Databases
HMDB0033712 HMDB
WO2004064830 Patent
View more database links
Registry Numbers Types Sources
1667250 Reaxys Registry Number Reaxys
66056-18-6 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
11575586 PubMed citation Europe PMC
12127165 PubMed citation Europe PMC
14608046 PubMed citation Europe PMC
14643306 PubMed citation Europe PMC
22074222 PubMed citation Europe PMC
Last Modified
13 November 2013