CHEBI:184373 - cremeomycin

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ChEBI Name cremeomycin
ChEBI ID CHEBI:184373
Definition A diazo compound that is cyclohexa-1,3-diene substituted by carboxy, methoxy, diazo and oxo groups at positions 1, 4, 5, and 6, respectively. It is an natural product isolated from Streptomyces cremeus.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
Download Molfile XML SDF
Formula C8H6N2O4
Net Charge 0
Average Mass 194.146
Monoisotopic Mass 194.03276
InChI InChI=1S/C8H6N2O4/c1-14-5-3-2-4(8(12)13)7(11)6(5)10-9/h2-3H,1H3,(H,12,13)
InChIKey HTCPEWKHGGGJBI-UHFFFAOYSA-N
SMILES COC1=CC=C(C(O)=O)C(=O)C1=[N+]=[N-]
Metabolite of Species Details
Streptomyces cremeus (NCBI:txid66881) See: PubMed
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): antibacterial agent
A substance (or active part thereof) that kills or slows the growth of bacteria.
bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
Application(s): antineoplastic agent
A substance that inhibits or prevents the proliferation of neoplasms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing cremeomycin (CHEBI:184373) has role antibacterial agent (CHEBI:33282)
cremeomycin (CHEBI:184373) has role antineoplastic agent (CHEBI:35610)
cremeomycin (CHEBI:184373) has role bacterial metabolite (CHEBI:76969)
cremeomycin (CHEBI:184373) is a cyclohexadiene (CHEBI:37613)
cremeomycin (CHEBI:184373) is a diazo compound (CHEBI:39444)
cremeomycin (CHEBI:184373) is a ether (CHEBI:25698)
cremeomycin (CHEBI:184373) is a monocarboxylic acid (CHEBI:25384)
cremeomycin (CHEBI:184373) is conjugate acid of cremeomycin(1−) (CHEBI:180678)
Incoming cremeomycin(1−) (CHEBI:180678) is conjugate base of cremeomycin (CHEBI:184373)
IUPAC Name
5-diazo-4-methoxy-6-oxocyclohexa-1,3-diene-1-carboxylic acid
Synonyms Sources
5-diazo-4-methoxy-6-oxo-1,3-cyclohexadiene-1-carboxylic acid ChEBI
antibiotic U 23643 ChEBI
U 23643 ChEBI
U-23,643 ChEBI
U-23643 ChEBI
Manual Xrefs Databases
28285805 ChemSpider
C00016531 KNApSAcK
US3350269 Patent
View more database links
Registry Number Type Source
11050-22-9 CAS Registry Number KNApSAcK
Citations Waiting for Citations Types Sources
26278892 PubMed citation Europe PMC
26689788 PubMed citation Europe PMC
29505698 PubMed citation Europe PMC
29771512 PubMed citation Europe PMC
30120394 PubMed citation Europe PMC
7622439 PubMed citation Europe PMC
Last Modified
24 November 2021