caerulomycin G (CHEBI:69226)

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ChEBI Name	caerulomycin G

ChEBI ID	CHEBI:69226

Definition	A pyridine alkaloid that is 2,2ʼ-bipyridine substituted at position 6 by a hydroxymethyl group and at positions 3 and 4 by methoxy groups respectively. 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

C13H14N2O3

Net Charge

Average Mass

246.26190

Monoisotopic Mass

246.10044

InChI

InChI=1S/C13H14N2O3/c1-17-11-7-9(8-16)15-12(13(11)18-2)10-5-3-4-6-14-10/h3-7,16H,8H2,1-2H3

InChIKey

NOWSJBQEOYCSBC-UHFFFAOYSA-N

SMILES

COc1cc(CO)nc(-c2ccccn2)c1OC

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 G (CHEBI:69226) has parent hydride 2,2'-bipyridine (CHEBI:30351) caerulomycin G (CHEBI:69226) has role antineoplastic agent (CHEBI:35610) caerulomycin G (CHEBI:69226) has role bacterial metabolite (CHEBI:76969) caerulomycin G (CHEBI:69226) has role marine metabolite (CHEBI:76507) caerulomycin G (CHEBI:69226) is a aromatic ether (CHEBI:35618) caerulomycin G (CHEBI:69226) is a bipyridines (CHEBI:50511) caerulomycin G (CHEBI:69226) is a monohydroxypyridine (CHEBI:38182) caerulomycin G (CHEBI:69226) is a pyridine alkaloid (CHEBI:26416)

IUPAC Name

(3,4-dimethoxy-2,2ʼ-bipyridin-6-yl)methanol

Registry Number	Type	Source
21856154	Reaxys Registry Number	Reaxys

Citation	Type	Source
21770434	PubMed citation	Europe PMC

Last Modified

02 December 2013