CHEBI:192287 - chaetocyclinone B

ChEBI IDCHEBI:192287
ChEBI Namechaetocyclinone B
Stars
DefinitionAn organic heterotricyclic compound that is 1H,10H-pyrano[4,3-b]chromene substituted by methyl, hydroxy, methoxy, methoxycarbonyl, and oxo groups at positions 3, 6, 7, 9 and 10, respectively. It is produced by cultures of Chaetomium sp. Gö 100/2, which was isolated from marine algae.
Last Modified6 June 2022
SubmitterAdnan
DownloadsMolfile
FormulaC16H14O7
Net Charge0
Average Mass318.281
Monoisotopic Mass318.07395
SMILESCOC(=O)c1cc(OC)c(O)c2oc3c(c(=O)c12)COC(C)=C3
InChIInChI=1S/C16H14O7/c1-7-4-10-9(6-22-7)13(17)12-8(16(19)21-3)5-11(20-2)14(18)15(12)23-10/h4-5,18H,6H2,1-3H3
InChIKeyTURYTCNCTQTGRQ-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Ascomycota sp. Ind19F07 (ncbitaxon:1583058) - PubMed (25537370)
Chaetomium sp. (ncbitaxon:1769349) - DOI (10.1002/ejoc.200601020) Strain: Gö 100/2
Phomopsis sp. HNY29-2B (ncbitaxon:1418122) - DOI (10.1002/cjoc.201700375)
Roles Classification
Biological Roles:
fungal metabolite  Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
marine metabolite  Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
ChEBI Ontology
Outgoing Relation(s)
chaetocyclinone B (CHEBI:192287) has role fungal metabolite (CHEBI:76946)
chaetocyclinone B (CHEBI:192287) has role marine metabolite (CHEBI:76507)
chaetocyclinone B (CHEBI:192287) is a aromatic ether (CHEBI:35618)
chaetocyclinone B (CHEBI:192287) is a cyclic ether (CHEBI:37407)
chaetocyclinone B (CHEBI:192287) is a cyclic ketone (CHEBI:3992)
chaetocyclinone B (CHEBI:192287) is a methyl ester (CHEBI:25248)
chaetocyclinone B (CHEBI:192287) is a organic heterotricyclic compound (CHEBI:26979)
chaetocyclinone B (CHEBI:192287) is a phenols (CHEBI:33853)
chaetocyclinone B (CHEBI:192287) is a polyketide (CHEBI:26188)
IUPAC Name 
methyl 6-hydroxy-7-methoxy-3-methyl-10-oxo-1H,10H-pyrano[4,3-b]chromene-9-carboxylate
Synonym  Source
methyl 6-hydroxy-7-methoxy-3-methyl-10-oxo-1H,10H-pyrano[4,3-b][1]benzopyran-9-carboxylateIUPAC
Citations