Ketcher 10152009472D 1   1.00000     0.00000     0

  6  5  0     0  0            999 V2000
    5.6617   -7.1754    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.5277   -6.6754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3937   -7.1754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2598   -6.6754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1258   -7.1754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2598   -5.6754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0     0  0
  2  3  1  0     0  0
  3  4  1  0     0  0
  4  5  1  0     0  0
  4  6  2  0     0  0
M  END
> <ID>
CHEBI:40823

> <NAME>
(aminooxy)acetic acid

> <DEFINITION>
A member of the class of hydroxylamines that is acetic acid substituted at postion 2 by an aminooxy group. It is a compound which inhibits aminobutyrate aminotransferase activity in vivo, resulting in increased levels of γ-aminobutyric acid in tissues.

> <STAR>
3

> <SYNONYM>
U-7524; carboxymethoxyamine; AOAA; AOA; aminooxyacetic acid; 2-aminooxyethanoic acid; 2-(aminooxy)acetic acid; (O-carboxymethyl)hydroxylamine; (carboxymethoxy)amine

> <IUPAC_NAME>
(aminooxy)acetic acid

> <FORMULA>
C2H5NO3

> <MASS>
91.066

> <MONOISOTOPIC_MASS>
91.02694

> <CHARGE>
0

> <SMILES>
NOCC(O)=O

> <INCHI>
InChI=1S/C2H5NO3/c3-6-1-2(4)5/h1,3H2,(H,4,5)

> <INCHIKEY>
NQRKYASMKDDGHT-UHFFFAOYSA-N

> <CAS_REGISTRY_NUMBER>
645-88-5

> <REAXYS_REGISTRY_NUMBER>
878238

> <CHEMIDPLUS>
645-88-5

> <DRUGBANK_ACCESSION>
DB02079

> <METACYC_ACCESSION>
CARBOXYMETHOXYLAMINE

> <PDBECHEM_ACCESSION>
AOA

> <WIKIPEDIA_ACCESSION>
Aminooxyacetic_acid

> <PUBMED_CITATION>
12234190; 12899834; 15480681; 15791207; 18687801; 20208150; 22128428; 25462081; 27157912; 27257787; 27639598; 28533892; 30127117; 31032581; 31410589; 31912705; 31930778; 32072910; 32194794; 3251251; 8930249

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