CHEBI:69235 - (Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime

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ChEBI Name (Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime
ChEBI ASCII Name (Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime
Definition A pyridine alkaloid that is 2,2ʼ-bipyridine substituted by a methoxy group at position 4 and a (Z)-(hydroxyimino)methyl group at position 6. It has been isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C12H11N3O2
Net Charge 0
Average Mass 229.23460
Monoisotopic Mass 229.08513
InChI InChI=1S/C12H11N3O2/c1-17-10-6-9(8-14-16)15-12(7-10)11-4-2-3-5-13-11/h2-8,16H,1H3/b14-8-
SMILES COc1cc(\C=N/O)nc(c1)-c1ccccn1
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.
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
(via alkaloid )
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ChEBI Ontology
Outgoing (Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime (CHEBI:69235) has parent hydride 2,2'-bipyridine (CHEBI:30351)
(Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime (CHEBI:69235) has role bacterial metabolite (CHEBI:76969)
(Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime (CHEBI:69235) has role marine metabolite (CHEBI:76507)
(Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime (CHEBI:69235) is a aldoxime (CHEBI:22307)
(Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime (CHEBI:69235) is a aromatic ether (CHEBI:35618)
(Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime (CHEBI:69235) is a bipyridines (CHEBI:50511)
(Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime (CHEBI:69235) is a pyridine alkaloid (CHEBI:26416)
Manual Xref Database
10401558 ChemSpider
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Registry Number Type Source
5744144 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
21770434 PubMed citation Europe PMC
Last Modified
28 April 2014