caerulomycin K (CHEBI:69230)

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ChEBI Name	caerulomycin K

ChEBI ID	CHEBI:69230

Definition	A pyridine alkaloid that is 2-phenylpyridine substituted by a methoxy group at position 4 and a (E)-(hydroxyimino)methyl 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

C13H12N2O2

Net Charge

Average Mass

228.24660

Monoisotopic Mass

228.08988

InChI

InChI=1S/C13H12N2O2/c1-17-12-7-11(9-14-16)15-13(8-12)10-5-3-2-4-6-10/h2-9,16H,1H3/b14-9+

InChIKey

PXFUULIZLQXHKZ-NTEUORMPSA-N

SMILES

COc1cc(\C=N\O)nc(c1)-c1ccccc1

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.

ChEBI Ontology
Outgoing	caerulomycin K (CHEBI:69230) has role antineoplastic agent (CHEBI:35610) caerulomycin K (CHEBI:69230) has role bacterial metabolite (CHEBI:76969) caerulomycin K (CHEBI:69230) has role marine metabolite (CHEBI:76507) caerulomycin K (CHEBI:69230) is a aldoxime (CHEBI:22307) caerulomycin K (CHEBI:69230) is a aromatic ether (CHEBI:35618) caerulomycin K (CHEBI:69230) is a pyridine alkaloid (CHEBI:26416)

IUPAC Name

(E)-N-hydroxy-1-(4-methoxy-6-phenylpyridin-2-yl)methanimine

Synonym	Source
(E)-4-methoxy-2-phenylpyridine-6-carbaldehyde oxime	ChEBI

Registry Number	Type	Source
21856152	Reaxys Registry Number	Reaxys

Citation	Type	Source
21770434	PubMed citation	Europe PMC

Last Modified

02 December 2013