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CHEBI:15429 - hydroxylamine
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  | | ChEBI Name | hydroxylamine | | ChEBI ID | CHEBI:15429 | | Definition | The simplest hydroxylamine, consisting of ammonia bearing a hydroxy substituent. It is an intermediate in the biological nitrification by microbes like bacteria. | | Stars |  This entity has been manually annotated by the ChEBI Team. | | Secondary ChEBI IDs | CHEBI:43221, CHEBI:5806, CHEBI:14421, CHEBI:10793, CHEBI:24708 | | Supplier Information | | Download | Molfile XML SDF | | - Find compounds which contain this structure
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| | | Wikipedia | License |  | | Read full article at Wikipedia | | Monoisotopic Mass | 33.02146 | | InChI | InChI=1S/H3NO/c1-2/h2H,1H2 | | InChIKey | AVXURJPOCDRRFD-UHFFFAOYSA-N | |
| Metabolite of Species | Details | | Chlamydomonas reinhardtii (NCBI:txid3055) | See: PubMed | | Roles Classification | | 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. | | 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 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 beta-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). | | nucleophilic reagent A reagent that forms a bond to its reaction partner (the electrophile) by donating both bonding electrons. | View more via ChEBI Ontology | ChEBI Ontology | | Outgoing | hydroxylamine (CHEBI:15429) has parent hydride ammonia (CHEBI:16134) hydroxylamine (CHEBI:15429) has role algal metabolite (CHEBI:84735) hydroxylamine (CHEBI:15429) has role bacterial xenobiotic metabolite (CHEBI:76976) hydroxylamine (CHEBI:15429) has role EC 1.1.3.13 (alcohol oxidase) inhibitor (CHEBI:63156) hydroxylamine (CHEBI:15429) has role EC 4.2.1.22 (cystathionine β-synthase) inhibitor (CHEBI:63157) hydroxylamine (CHEBI:15429) has role EC 4.3.1.10 (serine-sulfate ammonia-lyase) inhibitor (CHEBI:77090) hydroxylamine (CHEBI:15429) has role nitric oxide donor (CHEBI:50566) hydroxylamine (CHEBI:15429) has role nucleophilic reagent (CHEBI:59740) hydroxylamine (CHEBI:15429) is a hydroxylamines (CHEBI:24709) hydroxylamine (CHEBI:15429) is conjugate acid of aminooxidanide (CHEBI:29773) hydroxylamine (CHEBI:15429) is conjugate acid of hydroxyazanide (CHEBI:29772) | | Incoming | 2-acetamidofluorene N-sulfate (CHEBI:35424) has functional parent hydroxylamine (CHEBI:15429) 5-hydroxyamino-3-methylpyrrolidine-2-carboxylic acid (CHEBI:41101) has functional parent hydroxylamine (CHEBI:15429) N-acetoxyarylamine (CHEBI:21494) has functional parent hydroxylamine (CHEBI:15429) N-hydroxy-2-methylpropanamine (CHEBI:131928) has functional parent hydroxylamine (CHEBI:15429) N-hydroxy-4-aminobiphenyl O-sulfate (CHEBI:32701) has functional parent hydroxylamine (CHEBI:15429) N-{3-[(E)-(tert-butoxyimino)methyl]-4-chlorophenyl}-2-methylfuran-3-carbothioamide (CHEBI:47715) has functional parent hydroxylamine (CHEBI:15429) O-phosphonohydroxylamine (CHEBI:28048) has functional parent hydroxylamine (CHEBI:15429) vorinostat (CHEBI:45716) has functional parent hydroxylamine (CHEBI:15429) N-hydroxy-MeIQx (CHEBI:133915) is a hydroxylamine (CHEBI:15429) N-hydroxy-PhIP (CHEBI:133920) is a hydroxylamine (CHEBI:15429) aminooxidanide (CHEBI:29773) is conjugate base of hydroxylamine (CHEBI:15429) hydroxyazanide (CHEBI:29772) is conjugate base of hydroxylamine (CHEBI:15429) aminooxy group (CHEBI:29770) is substituent group from hydroxylamine (CHEBI:15429) hydroxyamino group (CHEBI:29769) is substituent group from hydroxylamine (CHEBI:15429) | | IUPAC Names | | dihydridohydroxidonitrogen | | hydroxylamine | | Synonyms | Sources | | [NH2OH] | IUPAC | | H2NHO | IUPAC | | HYDROXYAMINE | PDBeChem | Hydroxylamin  | ChEBI | | Hydroxylamine | KEGG COMPOUND | | hydroxylamine | UniProt | | oxyammonia | NIST Chemistry WebBook  | | Manual Xrefs | Databases | | C00192 | KEGG COMPOUND | | HMDB0003338 | HMDB | | HOA | PDBeChem | | Hydroxylamine | Wikipedia | | HYDROXYLAMINE | MetaCyc | | View more database links | | Registry Numbers | Types | Sources | | 3587190 | Reaxys Registry Number | Reaxys | | 478 | Gmelin Registry Number | Gmelin | | 7803-49-8 | CAS Registry Number | NIST Chemistry WebBook | | 7803-49-8 | CAS Registry Number | ChemIDplus | | 11053303 | PubMed citation | Europe PMC | | 11160411 | PubMed citation | Europe PMC | | 11226629 | PubMed citation | Europe PMC | | 11750265 | PubMed citation | Europe PMC | | 12962703 | PubMed citation | Europe PMC | | 17385063 | PubMed citation | Europe PMC | | 18399918 | PubMed citation | Europe PMC | | 18515490 | PubMed citation | Europe PMC | | 21185448 | PubMed citation | Europe PMC | | Last Modified | | 20 April 2017 | |
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