CHEBI:68807 - chaetoglobosin D

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ChEBI Name chaetoglobosin D
Definition A cytochalasan alkaloid found in Chaetomium globosum and Chaetomium brasiliense.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C32H36N2O5
Net Charge 0
Average Mass 528.63860
Monoisotopic Mass 528.262
InChI InChI=1S/C32H36N2O5/c1-17-8-7-10-23-30(38)20(4)19(3)28-25(15-21-16-33-24-11-6-5-9-22(21)24)34-31(39)32(23,28)27(36)13-12-26(35)29(37)18(2)14-17/h5-7,9-14,16-17,19,23,25,28-30,33,37-38H,4,8,15H2,1-3H3,(H,34,39)/b10-7+,13-12+,18-14+/t17-,19+,23-,25-,28-,29+,30+,32+/m0/s1
SMILES C[C@H]1[C@H]2[C@H](Cc3c[nH]c4ccccc34)NC(=O)[C@@]22[C@@H](\C=C\C[C@H](C)\C=C(C)\[C@@H](O)C(=O)\C=C\C2=O)[C@H](O)C1=C
Metabolite of Species Details
Chaetomium brasiliense (NCBI:txid155871) See: CiteXplore
Chaetomium globosum (NCBI:txid38033) See: PubMed
Roles Classification
Biological Role(s): Chaetomium metabolite
Any fungal metabolite produced during a metabolic reaction in the mould, Chaetomium.
fungal metabolite
Any eukaryotic metabolite produced during a metabolic reaction in fungi, the kingdom that includes microorganisms such as the yeasts and moulds.
(via cytochalasan alkaloid )
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing chaetoglobosin D (CHEBI:68807) has role Chaetomium metabolite (CHEBI:76960)
chaetoglobosin D (CHEBI:68807) has role antineoplastic agent (CHEBI:35610)
chaetoglobosin D (CHEBI:68807) is a cytochalasan alkaloid (CHEBI:75946)
chaetoglobosin D (CHEBI:68807) is a indoles (CHEBI:24828)
chaetoglobosin D (CHEBI:68807) is a macrocycle (CHEBI:51026)
chaetoglobosin D (CHEBI:68807) is a secondary α-hydroxy ketone (CHEBI:2468)
Database Link Database
4944492 Chemspider accession
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Registry Numbers Types Sources
55945-73-8 CAS Registry Number ChemIDplus
5786695 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
7116505 PubMed citation Europe PMC
Last Modified
06 February 2018