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CHEBI:65803 - dorsilurin F

Default Structure
ChEBI IDCHEBI:65803
ChEBI Namedorsilurin F
Stars
DefinitionA 7-hydroxyflavonol substituted by additional hydroxy groups at positions 5 and 3' and prenyl groups at positions 6, 8 and 4'. Isolated from the roots of Dorstenia psilurus, it exhibits α-glucosidase inhibitory activity.
Last Modified15 January 2013
DownloadsMolfile
FormulaC30H34O6
Net Charge0
Average Mass490.596
Monoisotopic Mass490.23554
SMILESCC(C)=CCc1ccc(-c2oc3c(CC=C(C)C)c(O)c(CC=C(C)C)c(O)c3c(=O)c2O)cc1O
InChIInChI=1S/C30H34O6/c1-16(2)7-10-19-11-12-20(15-23(19)31)29-28(35)27(34)24-26(33)21(13-8-17(3)4)25(32)22(30(24)36-29)14-9-18(5)6/h7-9,11-12,15,31-33,35H,10,13-14H2,1-6H3
InChIKeyBHIMYJSCHPQEQT-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Dorstenia psilurus (ncbitaxon:106723) root (BTO:0001188) PubMed (19061390)
Roles Classification
Biological Roles:
EC 3.2.1.20 (alpha-glucosidase) inhibitor  An EC 3.2.1.* (glycosidase) inhibitor that interferes with the action of α-glucosidase (EC 3.2.1.20).
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
ChEBI Ontology
Outgoing Relation(s)
dorsilurin F (CHEBI:65803) has role EC 3.2.1.20 (α-glucosidase) inhibitor (CHEBI:67239)
dorsilurin F (CHEBI:65803) has role metabolite (CHEBI:25212)
dorsilurin F (CHEBI:65803) is a 7-hydroxyflavonol (CHEBI:52267)
IUPAC Name 
3,5,7-trihydroxy-2-[3-hydroxy-4-(3-methylbut-2-en-1-yl)phenyl]-6,8-bis(3-methylbut-2-en-1-yl)-4H-chromen-4-one
Synonym  Source
6,8,4'-triprenyl-5,7,3'-trihydroxyflavonolChEBI
Registry NumbersSources
Reaxys:19384763Reaxys
Citations