CHEBI:155891 - dihydrogeodin

ChEBI IDCHEBI:155891
ChEBI Namedihydrogeodin
Stars
DefinitionA member of the class of benzophenones that is sulochrin in which the hydrogens at positions 3 and 5 are substituted by chloro groups. It is isolated from several Aspergillus species.
Last Modified18 June 2020
SubmitterAdnan
DownloadsMolfile
FormulaC17H14Cl2O7
Net Charge0
Average Mass401.198
Monoisotopic Mass400.01166
SMILESCOC(=O)c1cc(O)cc(OC)c1C(=O)c1c(O)c(Cl)c(C)c(Cl)c1O
InChIInChI=1S/C17H14Cl2O7/c1-6-12(18)15(22)11(16(23)13(6)19)14(21)10-8(17(24)26-3)4-7(20)5-9(10)25-2/h4-5,20,22-23H,1-3H3
InChIKeyAXIPUIQLQUNOCF-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Aspergillus terreus (ncbitaxon:33178)
- PubMed (29388436) Strain: TM8
- PubMed (27844127) Strain: QT122
Aspergillus flavipes (ncbitaxon:41900) - PubMed (27933892) Strain: HN4-13
Trewia nudiflora (ncbitaxon:300977) - PubMed (19140073)
Roles Classification
Biological Role:
Aspergillus metabolite  Any fungal metabolite produced during a metabolic reaction in the mould, Aspergillus .
ChEBI Ontology
Outgoing Relation(s)
dihydrogeodin (CHEBI:155891) has functional parent sulochrin (CHEBI:16159)
dihydrogeodin (CHEBI:155891) has role Aspergillus metabolite (CHEBI:76956)
dihydrogeodin (CHEBI:155891) is a aromatic ether (CHEBI:35618)
dihydrogeodin (CHEBI:155891) is a benzophenones (CHEBI:22726)
dihydrogeodin (CHEBI:155891) is a dichlorobenzene (CHEBI:23697)
dihydrogeodin (CHEBI:155891) is a methyl ester (CHEBI:25248)
dihydrogeodin (CHEBI:155891) is a phenols (CHEBI:33853)
dihydrogeodin (CHEBI:155891) is conjugate acid of dihydrogeodin(2−) (CHEBI:150012)
Incoming Relation(s)
dihydrogeodin(2−) (CHEBI:150012) is conjugate base of dihydrogeodin (CHEBI:155891)
IUPAC Name 
methyl 2-(3,5-dichloro-2,6-dihydroxy-4-methylbenzoyl)-5-hydroxy-3-methoxybenzoate
Synonyms  Source
2-[2,6-dihydroxy-3,5-dichloro-4-methylbenzoyl]-3-methoxy-5-hydroxybenzoic acid methyl esterChEBI
2-(3,5-dichloro-2,6-dihydroxy-4-methylbenzoyl)-5-hydroxy-3-methoxybenzoic acid methyl esterChEBI
Manual XrefsDatabases
C00000573KNApSAcK
Registry NumbersSources
CAS:2151-16-8ChemIDplus
Citations