CHEBI:69227 - caerulomycin H

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ChEBI Name caerulomycin H
ChEBI ID CHEBI:69227
Definition A pyridine alkaloid that is 2,2ʼ-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.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C11H9N3O2
Net Charge 0
Average Mass 215.20810
Monoisotopic Mass 215.06948
InChI InChI=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+
InChIKey XLFYSDMKBLTHTJ-NTUHNPAUSA-N
SMILES O\N=C\c1cc(O)cc(n1)-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.
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 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]-2,2ʼ-bipyridin-4-ol
Synonym Source
(E)-4-hydroxy-2,2ʼ-bipyridine-6-carbaldehyde oxime ChEBI
Registry Number Type Source
21856153 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
21770434 PubMed citation Europe PMC
Last Modified
02 December 2013