CHEBI:69232 - caerulomycin C

ChEBI IDCHEBI:69232
ChEBI Namecaerulomycin C
Stars
DefinitionA pyridine alkaloid that is 2,2'-bipyridine substituted by methoxy groups at positions 3 and 4 and a (E)-(hydroxyimino)methyl group at position 6. Isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus, it exhibits antineoplastic activity.
Last Modified28 April 2014
DownloadsMolfile
FormulaC13H13N3O3
Net Charge0
Average Mass259.265
Monoisotopic Mass259.09569
SMILESCOc1cc(/C=N/O)nc(-c2ccccn2)c1OC
InChIInChI=1S/C13H13N3O3/c1-18-11-7-9(8-15-17)16-12(13(11)19-2)10-5-3-4-6-14-10/h3-8,17H,1-2H3/b15-8+
InChIKeyWZBOHQZLZFLYKP-OVCLIPMQSA-N
Species of MetaboliteComponentSourceComments
Actinoalloteichus cyanogriseus (ncbitaxon:65497) - PubMed (21770434) Ethyl acetate extract of fermentation broth Strain: WH1 2216-6
Roles Classification
Biological Roles:
marine metabolite  Any metabolite produced during a metabolic reaction in marine macro- and microorganisms.
bacterial metabolite  Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
metabolite  Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
Application:
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
ChEBI Ontology
Outgoing Relation(s)
caerulomycin C (CHEBI:69232) has parent hydride 2,2'-bipyridine (CHEBI:30351)
caerulomycin C (CHEBI:69232) has role antineoplastic agent (CHEBI:35610)
caerulomycin C (CHEBI:69232) has role bacterial metabolite (CHEBI:76969)
caerulomycin C (CHEBI:69232) has role marine metabolite (CHEBI:76507)
caerulomycin C (CHEBI:69232) is a aldoxime (CHEBI:22307)
caerulomycin C (CHEBI:69232) is a aromatic ether (CHEBI:35618)
caerulomycin C (CHEBI:69232) is a bipyridines (CHEBI:50511)
caerulomycin C (CHEBI:69232) is a pyridine alkaloid (CHEBI:26416)
IUPAC Name 
(E)-1-(3,4-dimethoxy-2,2'-bipyridin-6-yl)-N-hydroxymethanimine
Manual XrefsDatabases
26618626ChemSpider
Registry NumbersSources
Reaxys:7485593Reaxys
Citations