CHEBI:69233 - caerulomycinamide

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ChEBI Name caerulomycinamide
ChEBI ID CHEBI:69233
Definition A pyridine alkaloid that is 2,2ʼ-bipyridine substituted by a methoxy group at position 4 and an aminocarbonyl group at position 6. Isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus, it exhibits antineoplastic activity.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C12H11N3O2
Net Charge 0
Average Mass 229.23460
Monoisotopic Mass 229.08513
InChI InChI=1S/C12H11N3O2/c1-17-8-6-10(9-4-2-3-5-14-9)15-11(7-8)12(13)16/h2-7H,1H3,(H2,13,16)
InChIKey GGOIWQPOOKIKRW-UHFFFAOYSA-N
SMILES COc1cc(nc(c1)-c1ccccn1)C(N)=O
Metabolite of Species Details
Actinoalloteichus cyanogriseus (NCBI:txid65497) Ethyl acetate extract of fermentation broth of strain WH1 2216-6 See: PubMed
Roles Classification
Biological Role(s): bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
marine metabolite
Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
metabolite
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 caerulomycinamide (CHEBI:69233) has parent hydride 2,2'-bipyridine (CHEBI:30351)
caerulomycinamide (CHEBI:69233) has role antineoplastic agent (CHEBI:35610)
caerulomycinamide (CHEBI:69233) has role bacterial metabolite (CHEBI:76969)
caerulomycinamide (CHEBI:69233) has role marine metabolite (CHEBI:76507)
caerulomycinamide (CHEBI:69233) is a aromatic ether (CHEBI:35618)
caerulomycinamide (CHEBI:69233) is a bipyridines (CHEBI:50511)
caerulomycinamide (CHEBI:69233) is a pyridine alkaloid (CHEBI:26416)
caerulomycinamide (CHEBI:69233) is a pyridinecarboxamide (CHEBI:25529)
IUPAC Name
4-methoxy-2,2ʼ-bipyridine-6-carboxamide
Synonym Source
4-methoxy-[2,2ʼ]bipyridinyl-6-carboxylic acid amide ChEBI
Registry Number Type Source
524935 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
21770434 PubMed citation Europe PMC
Last Modified
02 December 2013