CHEBI:68288 - methyl 3,8-dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate

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ChEBI Name methyl 3,8-dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate
ChEBI ID CHEBI:68288
ChEBI ASCII Name methyl 3,8-dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate
Definition A member of the class of xanthones that is 9H-xanthene substituted by a methyl group at position 6, hydroxy groups at positions 3 and 8, an oxo group at position 9 and a methoxy carbonyl at position 1. It has been isolated from Microdiplodia species and Aspergillus sydowii.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C16H12O6
Net Charge 0
Average Mass 300.26290
Monoisotopic Mass 300.06339
InChI InChI=1S/C16H12O6/c1-7-3-10(18)14-11(4-7)22-12-6-8(17)5-9(16(20)21-2)13(12)15(14)19/h3-6,17-18H,1-2H3
InChIKey MJOGVUMPZLEYIH-UHFFFAOYSA-N
SMILES COC(=O)c1cc(O)cc2oc3cc(C)cc(O)c3c(=O)c12
Metabolite of Species Details
Microdiplodia (NCBI:txid371130) EtOAc extract of an endophytic fungi isolated from Lycium intricatum of strain 9907 See: PubMed
Aspergillus sydowii (NCBI:txid75750) Ethyl acetate extract of culture broth, fungus isolated from a sea fan, Annella sp. of strain PSU F154 See: PubMed
Roles Classification
Biological Role(s): Aspergillus metabolite
Any fungal metabolite produced during a metabolic reaction in the mould, Aspergillus .
View more via ChEBI Ontology
ChEBI Ontology
Outgoing methyl 3,8-dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate (CHEBI:68288) has role Aspergillus metabolite (CHEBI:76956)
methyl 3,8-dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate (CHEBI:68288) is a aromatic ester (CHEBI:62732)
methyl 3,8-dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate (CHEBI:68288) is a methyl ester (CHEBI:25248)
methyl 3,8-dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate (CHEBI:68288) is a polyphenol (CHEBI:26195)
methyl 3,8-dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate (CHEBI:68288) is a xanthones (CHEBI:51149)
IUPAC Name
methyl 3,8-dihydroxy-6-methyl-9-oxo-9H-xanthene-1-carboxylate
Registry Number Type Source
304750 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
21244021 PubMed citation Europe PMC
21718031 PubMed citation Europe PMC
Last Modified
13 April 2015