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CHEBI ONTOLOGY - ANNOTATIONS

The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at http://www.ebi.ac.uk/chebi/. The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/). For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.
Term:L-3-oxoalanine
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Accession:CHEBI:37012 term browser browse the term
Definition:The L-enantiomer of 3-oxoalanine.
Synonyms:exact_synonym: (2S)-2-amino-3-oxopropanoic acid;   3-oxo-L-alanine
 related_synonym: 2-Aminomalonate semialdehyde;   2-Ammoniomalonate semialdehyde;   Formula=C3H5NO3;   InChI=1S/C3H5NO3/c4-2(1-5)3(6)7/h1-2H,4H2,(H,6,7)/t2-/m0/s1;   InChIKey=XMTCKNXTTXDPJX-REOHCLBHSA-N;   L-alpha-formylglycine;   SMILES=[H]C(=O)[C@H](N)C(O)=O
 alt_id: CHEBI:1020;   CHEBI:21210
 xref: KEGG:C11822
 cyclic_relationship: is_conjugate_acid_of CHEBI:58671;   is_tautomer_of CHEBI:77662


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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      application 0
        fuel 0
          methanol 0
            hydroxymethyl group 0
              serine 0
                L-serine 0
                  L-3-oxoalanine 0
                    L-3-oxoalanine residue 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 0
    subatomic particle 0
      composite particle 0
        hadron 0
          baryon 0
            nucleon 0
              atomic nucleus 0
                atom 0
                  main group element atom 0
                    p-block element atom 0
                      carbon group element atom 0
                        carbon atom 0
                          organic molecular entity 0
                            heteroorganic entity 0
                              organochalcogen compound 0
                                organooxygen compound 0
                                  carbon oxoacid 0
                                    carboxylic acid 0
                                      monocarboxylic acid 0
                                        fatty acid 0
                                          saturated fatty acid 0
                                            propionic acid 0
                                              alanine 0
                                                alanine derivative 0
                                                  3-oxoalanine 0
                                                    L-3-oxoalanine 0
                                                      L-3-oxoalanine residue 0
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