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The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at The data is made available under the Creative Commons License (CC 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.

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Accession:CHEBI:9611 term browser browse the term
Definition:A monocarboxylic acid amide in which 2,6-dimethylphenylaniline and isobutyric acid have combined to form the amide bond; used as a local anaesthetic.
Synonyms:exact_synonym: N-(2,6-dimethylphenyl)alaninamide
 related_synonym: 2-Amino-2',6'-propionoxylidide;   2-Amino-N-(2,6-dimethylphenyl)propionamid;   2-amino-N-(2,6-dimethylphenyl)propanamide;   Alanyl-2,6-xylidide;   Formula=C11H16N2O;   InChI=1S/C11H16N2O/c1-7-5-4-6-8(2)10(7)13-11(14)9(3)12/h4-6,9H,12H2,1-3H3,(H,13,14);   InChIKey=BUJAGSGYPOAWEI-UHFFFAOYSA-N;   SMILES=CC(N)C(=O)Nc1c(C)cccc1C;   tocainida;   tocainidum
 alt_id: CHEBI:106722
 xref: Beilstein:2416564;   CAS:41708-72-9;   DrugBank:DB01056;   Drug_Central:2686;   KEGG:C07142;   KEGG:D06172;   LINCS:LSM-1909;   PMID:12543515;   PMID:9989796;   Reaxys:2416564;   Wikipedia:Tocainide

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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      application 0
        pharmaceutical 0
          drug 0
            anaesthetic 0
              local anaesthetic 0
                tocainide 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
                            organic group 0
                              organic divalent group 0
                                organodiyl group 0
                                  carbonyl group 0
                                    carbonyl compound 0
                                      carboxylic acid 0
                                        carboacyl group 0
                                          univalent carboacyl group 0
                                            carbamoyl group 0
                                              carboxamide 0
                                                monocarboxylic acid amide 0
                                                  tocainide 0
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