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.
rat metabolite  Any mammalian metabolite produced during a metabolic reaction in rat (Rattus norvegicus).
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.
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.
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.
bacterial xenobiotic metabolite  Any bacterial metabolite produced by metabolism of a xenobiotic compound in bacteria.
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).
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).
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).
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.
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