CHEBI:67617 - 4ʼ-epichaetoviridin F

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ChEBI Name 4ʼ-epichaetoviridin F
ChEBI ID CHEBI:67617
ChEBI ASCII Name 4'-epichaetoviridin F
Definition An azaphilone that is 6H-furo[2,3-h]isochromene-6,8(6aH)-dione substituted by a chloro group at position 5, a methyl group at position 6a, a 2-methylbutanoyl group at position 9 and a 3-methylpent-1-en-1-yl group at position 3. It has been isolated from Chaetomium globosum.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C23H25ClO5
Net Charge 0
Average Mass 416.89500
Monoisotopic Mass 416.13905
InChI InChI=1S/C23H25ClO5/c1-6-12(3)8-9-14-10-15-16(11-28-14)18-17(20(25)13(4)7-2)22(27)29-23(18,5)21(26)19(15)24/h8-13H,6-7H2,1-5H3/b9-8+/t12-,13+,23-/m0/s1
InChIKey SPBQVEOEFQCPDM-YMWLQJPLSA-N
SMILES CC[C@H](C)\C=C\C1=CC2=C(Cl)C(=O)[C@@]3(C)OC(=O)C(C(=O)[C@H](C)CC)=C3C2=CO1
Metabolite of Species Details
Chaetomium globosum (NCBI:txid38033) Found in mycelium (BTO:0001436). Endophytic fungus in leaves of Viguiera robusta, EtOAc extract of culture broth and mycelium See: PubMed
Chaetomium globosum (NCBI:txid38033) See: PubMed
Roles Classification
Biological Role(s): fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
(via azaphilone )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 4ʼ-epichaetoviridin F (CHEBI:67617) is a γ-lactone (CHEBI:37581)
4ʼ-epichaetoviridin F (CHEBI:67617) is a azaphilone (CHEBI:50941)
4ʼ-epichaetoviridin F (CHEBI:67617) is a enone (CHEBI:51689)
4ʼ-epichaetoviridin F (CHEBI:67617) is a organic heterotricyclic compound (CHEBI:26979)
4ʼ-epichaetoviridin F (CHEBI:67617) is a organochlorine compound (CHEBI:36683)
IUPAC Name
(6aS)-5-chloro-6a-methyl-9-[(2R)-2-methylbutanoyl]-3-[(1E,3S)-3-methylpent-1-en-1-yl]-6H-furo[2,3-h]isochromene-6,8(6aH)-dione
Registry Number Type Source
21577523 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
21548578 PubMed citation Europe PMC
Last Modified
15 October 2013