CHEBI:67402 - 3ʼʼ-deoxy-6ʼ-O-desmethylcandidusin B

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ChEBI Name 3ʼʼ-deoxy-6ʼ-O-desmethylcandidusin B
ChEBI ASCII Name 3''-deoxy-6'-O-desmethylcandidusin B
Definition A member of the class of dibenzofurans that is dibenzo[b,d]furan substituted by a 4-hydroxyphenyl group at position 3, hydroxy groups at positions 1, 7 and 8 and a methoxy group at position 4. It has been isolated from the culture of the mangrove endophytic fungus Penicillium chermesinum.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C19H14O6
Net Charge 0
Average Mass 338.31090
Monoisotopic Mass 338.07904
InChI InChI=1S/C19H14O6/c1-24-18-11(9-2-4-10(20)5-3-9)6-15(23)17-12-7-13(21)14(22)8-16(12)25-19(17)18/h2-8,20-23H,1H3
SMILES COc1c(cc(O)c2c3cc(O)c(O)cc3oc12)-c1ccc(O)cc1
Metabolite of Species Details
Penicillium chermesinum (NCBI:txid63820) Ethylacetate extract of endophytic fungus isolated from stem of the mangrove plant Kandelia candel of strain ZH4 E2 See: PubMed
Roles Classification
Biological Role(s): EC (acetylcholinesterase) inhibitor
An EC 3.1.1.* (carboxylic ester hydrolase) inhibitor that interferes with the action of enzyme acetylcholinesterase (EC, which helps breaking down of acetylcholine into choline and acetic acid.
Penicillium metabolite
Any fungal metabolite produced during a metabolic reaction in Penicillium.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 3ʼʼ-deoxy-6ʼ-O-desmethylcandidusin B (CHEBI:67402) has role Penicillium metabolite (CHEBI:76964)
3ʼʼ-deoxy-6ʼ-O-desmethylcandidusin B (CHEBI:67402) has role EC (acetylcholinesterase) inhibitor (CHEBI:38462)
3ʼʼ-deoxy-6ʼ-O-desmethylcandidusin B (CHEBI:67402) is a aromatic ether (CHEBI:35618)
3ʼʼ-deoxy-6ʼ-O-desmethylcandidusin B (CHEBI:67402) is a dibenzofurans (CHEBI:38922)
3ʼʼ-deoxy-6ʼ-O-desmethylcandidusin B (CHEBI:67402) is a polyphenol (CHEBI:26195)
Registry Number Type Source
21548623 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
21510637 PubMed citation Europe PMC
Last Modified
13 January 2014