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CHEBI:69082 - licoricidin

ChEBI IDCHEBI:69082
ChEBI Namelicoricidin
Stars
DefinitionA member of the class of hydroxyisoflavans that is R-isoflavan with hydroxy groups at positions 7, 2' and 4', a methoxy group at position 5 and prenyl groups at positions 6 and 3'. Isolated from Glycyrrhiza uralensis, it exhibits antibacterial activity.
Last Modified28 July 2014
DownloadsMolfile
FormulaC26H32O5
Net Charge0
Average Mass424.537
Monoisotopic Mass424.22497
SMILES[H][C@@]1(c2ccc(O)c(CC=C(C)C)c2O)COc2cc(O)c(CC=C(C)C)c(OC)c2C1
InChIInChI=1S/C26H32O5/c1-15(2)6-8-19-22(27)11-10-18(25(19)29)17-12-21-24(31-14-17)13-23(28)20(26(21)30-5)9-7-16(3)4/h6-7,10-11,13,17,27-29H,8-9,12,14H2,1-5H3/t17-/m0/s1
InChIKeyGBRZTUJCDFSIHM-KRWDZBQOSA-N
Species of MetaboliteComponentSourceComments
Glycyrrhiza uralensis (ncbitaxon:74613) root (BTO:0001188) PubMed (22074222) Dried and ground roots extracted with supercritical CO2 with 5% EtOH as modifier
Roles Classification
Biological Roles:
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.
ChEBI Ontology
Outgoing Relation(s)
licoricidin (CHEBI:69082) has role antibacterial agent (CHEBI:33282)
licoricidin (CHEBI:69082) has role plant metabolite (CHEBI:76924)
licoricidin (CHEBI:69082) is a aromatic ether (CHEBI:35618)
licoricidin (CHEBI:69082) is a hydroxyisoflavans (CHEBI:76250)
licoricidin (CHEBI:69082) is a methoxyisoflavan (CHEBI:77002)
Incoming Relation(s)
licorisoflavan A (CHEBI:69083) has functional parent licoricidin (CHEBI:69082)
IUPAC Name 
4-[(3R)-7-hydroxy-5-methoxy-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  Source
4-((R)-7-hydroxy-5-methoxy-6-(3-methyl-but-2-enyl)-1-benzopyran-3-yl)-2-((E)-3-methyl-but-2-enyl)-benzene-1,3-diolChemIDplus
2',4',7'-trihydroxy-5-methoxy-3',6-diisopentenyl-isoflavanChEBI
Manual XrefsDatabases
LMPK12080045LIPID MAPS
C16986KEGG COMPOUND
Registry NumbersSources
Reaxys:5362788Reaxys
CAS:30508-27-1ChemIDplus
CAS:30508-27-1KEGG COMPOUND
Citations