CHEBI:133915 - N-hydroxy-MeIQx

ChEBI IDCHEBI:133915
ChEBI NameN-hydroxy-MeIQx
Stars
ASCII NameN-hydroxy-MeIQx
DefinitionAn imidazoquinoxaline that is 3H-imidazo[4,5-f]quinoxaline substituted at positions 3 and 8 by methyl groups and at position 2 by a hydroxyamino group. The active metabolite of the dietary carcinogen MeIQx.
Last Modified20 April 2017
SubmitterKeeva
DownloadsMolfile
FormulaC11H11N5O
Net Charge0
Average Mass229.243
Monoisotopic Mass229.09636
SMILESCc1cnc2ccc3c(nc(NO)n3C)c2n1
InChIInChI=1S/C11H11N5O/c1-6-5-12-7-3-4-8-10(9(7)13-6)14-11(15-17)16(8)2/h3-5,17H,1-2H3,(H,14,15)
InChIKeyFVNCCTJGBOTWTM-UHFFFAOYSA-N
Species of MetaboliteComponentSourceComments
Apis cerana (ncbitaxon:7461) - MetaboLights (MTBLS379)
Homo Sapiens (ncbitaxon:9606) urine (BTO:0001419) PubMed (10503894)
Rattus norvegicus (ncbitaxon:10116) - PubMed (11453738)
Roles Classification
Chemical Roles:
nitric oxide donor  An agent, with unique chemical structure and biochemical requirements, which generates nitric oxide.
nucleophilic reagent  A reagent that forms a bond to its reaction partner (the electrophile) by donating both bonding electrons.
Biological Roles:
mutagen  An agent that increases the frequency of mutations above the normal background level, usually by interacting directly with DNA and causing it damage, including base substitution.
carcinogenic agent  A role played by a chemical compound which is known to induce a process of carcinogenesis by corrupting normal cellular pathways, leading to the acquistion of tumoral capabilities.
human xenobiotic metabolite  Any human metabolite produced by metabolism of a xenobiotic compound in humans.
human urinary metabolite  Any metabolite (endogenous or exogenous) found in human urine samples.
genotoxin  A role played by a chemical compound to induce direct or indirect DNA damage. Such damage can potentially lead to the formation of a malignant tumour, but DNA damage does not lead inevitably to the creation of cancerous cells.
rat metabolite  Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
EC 1.1.3.13 (alcohol oxidase) inhibitor  An EC 1.1.3.* (oxidoreductase acting on donor CH-OH group, oxygen as acceptor) inhibitor that interferes with the action of alcohol oxidase (EC 1.1.3.13).
bacterial xenobiotic metabolite  Any bacterial metabolite produced by metabolism of a xenobiotic compound in bacteria.
algal metabolite  Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae.
EC 4.2.1.22 (cystathionine beta-synthase) inhibitor  An EC 4.2.1.* (hydro-lyases) inhibitor that interferes with the action of cystathionine β-synthase (EC 4.2.1.22).
EC 4.3.1.10 (serine-sulfate ammonia-lyase) inhibitor  An EC 4.3.1.* (ammonia-lyase) inhibitor that interferes with the action of serine-sulfate ammonia-lyase (EC 4.3.1.10).
Application:
nucleophilic reagent  A reagent that forms a bond to its reaction partner (the electrophile) by donating both bonding electrons.
ChEBI Ontology
Outgoing Relation(s)
N-hydroxy-MeIQx (CHEBI:133915) has functional parent MeIQx (CHEBI:76604)
N-hydroxy-MeIQx (CHEBI:133915) has role carcinogenic agent (CHEBI:50903)
N-hydroxy-MeIQx (CHEBI:133915) has role genotoxin (CHEBI:50902)
N-hydroxy-MeIQx (CHEBI:133915) has role human urinary metabolite (CHEBI:84087)
N-hydroxy-MeIQx (CHEBI:133915) has role human xenobiotic metabolite (CHEBI:76967)
N-hydroxy-MeIQx (CHEBI:133915) has role mutagen (CHEBI:25435)
N-hydroxy-MeIQx (CHEBI:133915) has role rat metabolite (CHEBI:86264)
N-hydroxy-MeIQx (CHEBI:133915) is a hydroxylamine (CHEBI:15429)
N-hydroxy-MeIQx (CHEBI:133915) is a imidazoquinoxaline (CHEBI:76605)
IUPAC Name 
N-(3,8-dimethyl-1,3-dihydro-2H-imidazo[4,5-f]quinoxalin-2-ylidene)hydroxylamine
Synonyms  Source
2-hydroxyamino-3,8-dimethylimidazo[4,5-f]quinoxalineChEBI
3,8-dimethyl-1,3-dihydro-2H-imidazo(4,5-f)quinoxalin-2-one oximeChemIDplus
N-hydroxy-methyl-IQXChemIDplus
N-OH-MeIQxChEBI
Manual XrefsDatabases
C20291KEGG COMPOUND
Registry NumbersSources
Reaxys:8146608Reaxys
CAS:115044-41-2ChemIDplus
CAS:115044-41-2KEGG COMPOUND
Citations