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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:dihydroorotic acid
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Accession:CHEBI:30865 term browser browse the term
Definition:A pyrimidinemonocarboxylic acid that results from the base-catalysed cyclisation of N(alpha)-carbethoxyasparagine.
Synonyms:exact_synonym: 2,6-dioxohexahydropyrimidine-4-carboxylic acid
 related_synonym: 4,5-dihydroorotic acid;   5,6-dihydro-orotic acid;   DL-dihydroortotic acid;   Formula=C5H6N2O4;   Hydroorotic acid;   InChI=1S/C5H6N2O4/c8-3-1-2(4(9)10)6-5(11)7-3/h2H,1H2,(H,9,10)(H2,6,7,8,11);   InChIKey=UFIVEPVSAGBUSI-UHFFFAOYSA-N;   SMILES=OC(=O)C1CC(=O)NC(=O)N1
 xref: Beilstein:155267;   Beilstein:83959;   CAS:155-54-4;   DrugBank:DB02129
 xref_mesh: MESH:C004768
 xref: Patent:US2773872;   Reaxys:83959;   Wikipedia:4\,5-Dihydroorotic_acid
 cyclic_relationship: is_conjugate_acid_of CHEBI:30867

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Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            orotic acid 0
              dihydroorotic acid 0
                (R)-dihydroorotic acid 0
                (S)-dihydroorotic acid 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
                                      carboacyl group 0
                                        univalent carboacyl group 0
                                          carbamoyl group 0
                                            carboxamide 0
                                              monocarboxylic acid amide 0
                                                urea 0
                                                  ureas 0
                                                    N-acylurea 0
                                                      dihydroorotic acid 0
                                                        (R)-dihydroorotic acid 0
                                                        (S)-dihydroorotic acid 0
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