CHEBI:68721 - mollicellin F

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ChEBI Name mollicellin F
ChEBI ID CHEBI:68721
Definition A member of the class of depsidones that is 3,4-dihydro-H,11H-chromeno[6,7-b][1,4]benzodioxepine substituted by a chloro group at position 9, hydroxy groups at positions 8 and 13, methyl groups at positions 2, 2, 5 and 10, oxo groups at positions 4 and 11 and a formyl group at position 7. Isolated from Chaetomium brasiliense, it exhibits cytotoxic activity.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C21H17ClO8
Net Charge 0
Average Mass 432.80800
Monoisotopic Mass 432.06120
InChI InChI=1S/C21H17ClO8/c1-7-12-17(9(6-23)14(25)13(7)22)28-16-8(2)11-10(24)5-21(3,4)30-18(11)15(26)19(16)29-20(12)27/h6,25-26H,5H2,1-4H3
InChIKey BUWVABSQGVRXOI-UHFFFAOYSA-N
SMILES Cc1c(Cl)c(O)c(C=O)c2Oc3c(C)c4C(=O)CC(C)(C)Oc4c(O)c3OC(=O)c12
Metabolite of Species Details
Chaetomium brasiliense (NCBI:txid155871) See: PubMed
Roles Classification
Biological Role(s): Chaetomium metabolite
Any fungal metabolite produced during a metabolic reaction in the mould, Chaetomium.
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via depsidones )
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing mollicellin F (CHEBI:68721) has role Chaetomium metabolite (CHEBI:76960)
mollicellin F (CHEBI:68721) has role antineoplastic agent (CHEBI:35610)
mollicellin F (CHEBI:68721) is a aldehyde (CHEBI:17478)
mollicellin F (CHEBI:68721) is a depsidones (CHEBI:75939)
mollicellin F (CHEBI:68721) is a organic heterotetracyclic compound (CHEBI:38163)
mollicellin F (CHEBI:68721) is a organochlorine compound (CHEBI:36683)
mollicellin F (CHEBI:68721) is a polyphenol (CHEBI:26195)
IUPAC Name
9-chloro-8,13-dihydroxy-2,2,5,10-tetramethyl-4,11-dioxo-3,4-dihydro-2H,11H-chromeno[6,7-b][1,4]benzodioxepine-7-carbaldehyde
Manual Xrefs Databases
134713 ChemSpider
HMDB0033338 HMDB
View more database links
Registry Numbers Types Sources
19895970 Reaxys Registry Number Reaxys
68455-12-9 CAS Registry Number Reaxys
Citation Waiting for Citations Type Source
19663417 PubMed citation Europe PMC
Last Modified
16 October 2013