CHEBI:65413 - antimycin A9

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ChEBI Name antimycin A9
ChEBI ID CHEBI:65413
Definition A benzamide obtained by formal condensation of the carboxy group of 3-formamido-2-hydroxybenzoic acid with the amino group of 3-amino-8-butyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl phenylacetate. It is a microbial metabolite isolated from Streptomyces.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C29H34N2O9
Net Charge 0
Average Mass 554.58830
Monoisotopic Mass 554.22643
InChI InChI=1S/C29H34N2O9/c1-4-5-12-21-26(40-23(33)15-19-10-7-6-8-11-19)18(3)39-29(37)24(17(2)38-28(21)36)31-27(35)20-13-9-14-22(25(20)34)30-16-32/h6-11,13-14,16-18,21,24,26,34H,4-5,12,15H2,1-3H3,(H,30,32)(H,31,35)
InChIKey NAEDADOYRYAJDM-UHFFFAOYSA-N
SMILES [H]C(=O)Nc1cccc(C(=O)NC2C(C)OC(=O)C(CCCC)C(OC(=O)Cc3ccccc3)C(C)OC2=O)c1O
Metabolite of Species Details
Streptomyces sp. (NCBI:txid1931) of strain K01-0031 See: PubMed
Roles Classification
Biological Role(s): metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
antimicrobial agent
A substance that kills or slows the growth of microorganisms, including bacteria, viruses, fungi and protozoans.
Application(s): nematicide
A substance used to destroy pests of the phylum Nematoda (roundworms).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing antimycin A9 (CHEBI:65413) has functional parent phenylacetic acid (CHEBI:30745)
antimycin A9 (CHEBI:65413) has role antimicrobial agent (CHEBI:33281)
antimycin A9 (CHEBI:65413) has role metabolite (CHEBI:25212)
antimycin A9 (CHEBI:65413) has role nematicide (CHEBI:25491)
antimycin A9 (CHEBI:65413) is a benzamides (CHEBI:22702)
antimycin A9 (CHEBI:65413) is a formamides (CHEBI:24079)
antimycin A9 (CHEBI:65413) is a macrodiolide (CHEBI:145556)
antimycin A9 (CHEBI:65413) is a phenols (CHEBI:33853)
IUPAC Name
8-butyl-3-{[3-formamido-2-hydroxybenzoyl]amino}-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl phenylacetate
Registry Number Type Source
21457547 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
15813185 PubMed citation Europe PMC
Last Modified
02 December 2019