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CHEBI:69227 - caerulomycin H

ChEBI IDCHEBI:69227
ChEBI Namecaerulomycin H
Stars
DefinitionA pyridine alkaloid that is 2,2'-bipyridine substituted by a hydroxy 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.
Last Modified2 December 2013
DownloadsMolfile
FormulaC11H9N3O2
Net Charge0
Average Mass215.212
Monoisotopic Mass215.06948
SMILESO/N=C/c1cc(O)cc(-c2ccccn2)n1
InChIInChI=1S/C11H9N3O2/c15-9-5-8(7-13-16)14-11(6-9)10-3-1-2-4-12-10/h1-7,16H,(H,14,15)/b13-7+
InChIKeyXLFYSDMKBLTHTJ-NTUHNPAUSA-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 H (CHEBI:69227) has parent hydride 2,2'-bipyridine (CHEBI:30351)
caerulomycin H (CHEBI:69227) has role antineoplastic agent (CHEBI:35610)
caerulomycin H (CHEBI:69227) has role bacterial metabolite (CHEBI:76969)
caerulomycin H (CHEBI:69227) has role marine metabolite (CHEBI:76507)
caerulomycin H (CHEBI:69227) is a aldoxime (CHEBI:22307)
caerulomycin H (CHEBI:69227) is a bipyridines (CHEBI:50511)
caerulomycin H (CHEBI:69227) is a monohydroxypyridine (CHEBI:38182)
caerulomycin H (CHEBI:69227) is a pyridine alkaloid (CHEBI:26416)
IUPAC Name 
6-[(E)-(hydroxyimino)methyl]-2,2'-bipyridin-4-ol
Synonym  Source
(E)-4-hydroxy-2,2'-bipyridine-6-carbaldehyde oximeChEBI
Registry NumbersSources
Reaxys:21856153Reaxys
Citations