CHEBI:66541 - laccaridione B

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ChEBI Name laccaridione B
ChEBI ID CHEBI:66541
Definition An organic heterotricyclic compound that is 1H-benzo[g]isochromene-8,9-dione substituted by an ethoxy group at position 1, hydroxy group at position 10, a methoxy group at position 7 and a 4-methylhex-2-en-2-yl group at position 3. Isolated from the stem of the fruiting bodies of the basidiomycete strain Laccaria amethystea, it exhibits inhibitory activity against proteases.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C23H26O6
Net Charge 0
Average Mass 398.44890
Monoisotopic Mass 398.17294
InChI InChI=1S/C23H26O6/c1-6-12(3)8-13(4)16-10-15-9-14-11-17(27-5)20(24)22(26)18(14)21(25)19(15)23(29-16)28-7-2/h8-12,23,25H,6-7H2,1-5H3/b13-8+
InChIKey UMMLLCGZZRNVRG-MDWZMJQESA-N
SMILES CCOC1OC(=Cc2cc3C=C(OC)C(=O)C(=O)c3c(O)c12)\C(C)=C\C(C)CC
Metabolite of Species Details
Laccaria amethystea (NCBI:txid213150) 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.
protease inhibitor
A compound which inhibits or antagonizes the biosynthesis or actions of proteases (endopeptidases).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing laccaridione B (CHEBI:66541) has role metabolite (CHEBI:25212)
laccaridione B (CHEBI:66541) has role protease inhibitor (CHEBI:37670)
laccaridione B (CHEBI:66541) is a cyclic acetal (CHEBI:59770)
laccaridione B (CHEBI:66541) is a enol ether (CHEBI:47985)
laccaridione B (CHEBI:66541) is a isochromenes (CHEBI:38761)
laccaridione B (CHEBI:66541) is a organic heterotricyclic compound (CHEBI:26979)
laccaridione B (CHEBI:66541) is a orthoquinones (CHEBI:25622)
laccaridione B (CHEBI:66541) is a phenols (CHEBI:33853)
IUPAC Name
1-ethoxy-10-hydroxy-7-methoxy-3-[(2E)-4-methylhex-2-en-2-yl]-1H-benzo[g]isochromene-8,9-dione
Manual Xrefs Databases
DE10037982 Patent
DE10349511 Patent
View more database links
Registry Number Type Source
8726721 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
11213295 PubMed citation Europe PMC
18422912 PubMed citation Europe PMC
Last Modified
06 June 2016