CHEBI:69083 - licorisoflavan A

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ChEBI Name licorisoflavan A
ChEBI ID CHEBI:69083
Definition A member of the class of hydroxyisoflavans that is the 7-O-methyl derivative of licoricidin. 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 C27H34O5
Net Charge 0
Average Mass 438.55590
Monoisotopic Mass 438.24062
InChI InChI=1S/C27H34O5/c1-16(2)7-9-20-23(28)12-11-19(26(20)29)18-13-22-25(32-15-18)14-24(30-5)21(27(22)31-6)10-8-17(3)4/h7-8,11-12,14,18,28-29H,9-10,13,15H2,1-6H3/t18-/m0/s1
InChIKey GDAAEAXMNLVRCZ-SFHVURJKSA-N
SMILES COc1cc2OC[C@H](Cc2c(OC)c1CC=C(C)C)c1ccc(O)c(CC=C(C)C)c1O
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): 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 licorisoflavan A (CHEBI:69083) has functional parent licoricidin (CHEBI:69082)
licorisoflavan A (CHEBI:69083) has role antibacterial agent (CHEBI:33282)
licorisoflavan A (CHEBI:69083) has role plant metabolite (CHEBI:76924)
licorisoflavan A (CHEBI:69083) is a aromatic ether (CHEBI:35618)
licorisoflavan A (CHEBI:69083) is a hydroxyisoflavans (CHEBI:76250)
licorisoflavan A (CHEBI:69083) is a methoxyisoflavan (CHEBI:77002)
IUPAC Name
4-[(3R)-5,7-dimethoxy-6-(3-methylbut-2-en-1-yl)-3,4-dihydro-2H-chromen-3-yl]-2-(3-methylbut-2-en-1-yl)benzene-1,3-diol
Synonyms Sources
(+)-2ʼ,4ʼ-dihydroxy-5,7-dimethoxy-6,3ʼ-diprenylisoflavan LIPID MAPS
5-O-methyllicoricidin ChemIDplus
7-O-methyllicoricidin ChEBI
Manual Xrefs Databases
HMDB0034184 HMDB
LMPK12080046 LIPID MAPS
View more database links
Registry Numbers Types Sources
129314-37-0 CAS Registry Number ChemIDplus
5461708 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
22074222 PubMed citation Europe PMC
Last Modified
16 January 2014