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CHEBI:65746 - 5-deoxyglyasperin F

Default Structure
ChEBI IDCHEBI:65746
ChEBI Name5-deoxyglyasperin F
Stars
DefinitionA hydroxyisoflavanone that is 2,3-dihydro-2'H,4H-3,8'-bichromen-4-one substituted by hydroxy groups at positions 5' and 7 and geminal methyl groups at position 2'. Isolated from the roots of Erythrina lysistemon, it exhibits anti-HIV activity.
Last Modified12 March 2013
DownloadsMolfile
FormulaC20H18O5
Net Charge0
Average Mass338.359
Monoisotopic Mass338.11542
SMILESCC1(C)C=Cc2c(O)ccc(C3COc4cc(O)ccc4C3=O)c2O1
InChIInChI=1S/C20H18O5/c1-20(2)8-7-13-16(22)6-5-12(19(13)25-20)15-10-24-17-9-11(21)3-4-14(17)18(15)23/h3-9,15,21-22H,10H2,1-2H3
InChIKeyNUHWTADXTBESTA-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Erythrina lysistemon (ncbitaxon:347910) root (BTO:0001188) PubMed (9170286)
Roles Classification
Biological Roles:
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
anti-HIV agent  An antiviral agent that destroys or inhibits the replication of the human immunodeficiency virus.
ChEBI Ontology
Outgoing Relation(s)
5-deoxyglyasperin F (CHEBI:65746) has role anti-HIV agent (CHEBI:64946)
5-deoxyglyasperin F (CHEBI:65746) has role metabolite (CHEBI:25212)
5-deoxyglyasperin F (CHEBI:65746) is a hydroxyisoflavanone (CHEBI:72739)
5-deoxyglyasperin F (CHEBI:65746) is a polyphenol (CHEBI:26195)
IUPAC Name 
5',7-dihydroxy-2',2'-dimethyl-2,3-dihydro-2'H,4H-3,8'-bichromen-4-one
Citations