CHEBI:184373 - cremeomycin

ChEBI IDCHEBI:184373
ChEBI Namecremeomycin
Stars
DefinitionA 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.
Last Modified24 November 2021
SubmitterAdnan
DownloadsMolfile
FormulaC8H6N2O4
Net Charge0
Average Mass194.146
Monoisotopic Mass194.03276
SMILESCOC1=CC=C(C(=O)O)C(=O)C1=[N+]=[N-]
InChIInChI=1S/C8H6N2O4/c1-14-5-3-2-4(8(12)13)7(11)6(5)10-9/h2-3H,1H3,(H,12,13)
InChIKeyHTCPEWKHGGGJBI-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Streptomyces cremeus (ncbitaxon:66881) - PubMed (7622439)
Roles Classification
Chemical Role:
Bronsted acid  A molecular entity capable of donating a hydron to an acceptor (Brønsted base).
Biological Roles:
bacterial metabolite  Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
antibacterial agent  A substance (or active part thereof) that kills or slows the growth of bacteria.
Application:
antineoplastic agent  A substance that inhibits or prevents the proliferation of neoplasms.
ChEBI Ontology
Outgoing Relation(s)
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 Relation(s)
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  Source
5-diazo-4-methoxy-6-oxo-1,3-cyclohexadiene-1-carboxylic acidChEBI
U 23643ChEBI
antibiotic U 23643ChEBI
U-23,643ChEBI
U-23643ChEBI
Manual XrefsDatabases
C00016531KNApSAcK
US3350269Patent
28285805ChemSpider
Registry NumbersSources
CAS:11050-22-9KNApSAcK
Citations