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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:thioacetamide
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Accession:CHEBI:32497 term browser browse the term
Definition:A thiocarboxamide consiting of acetamide having the oxygen replaced by sulfur.
Synonyms:exact_synonym: ethanethioamide
 related_synonym: Acetothioamide;   Formula=C2H5NS;   InChI=1S/C2H5NS/c1-2(3)4/h1H3,(H2,3,4);   InChIKey=YUKQRDCYNOVPGJ-UHFFFAOYSA-N;   SMILES=CC(N)=S;   TAA;   Thiacetamide;   Thioacetimidic acid;   Thioactamide;   acetic acid thioamide;   methylthioamide
 xref: Beilstein:506006;   CAS:62-55-5;   KEGG:C19302
 xref_mesh: MESH:D013853
 xref: PMID:20138653;   PMID:20534638;   PMID:20931291;   PMID:21182490;   PMID:21455425;   PMID:21489598;   PMID:21647311;   PMID:21699073;   PMID:21733084;   PMID:21733883;   PMID:21749370;   Reaxys:506006;   Wikipedia:Thioacetamide

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Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      biological role 0
        aetiopathogenetic role 0
          hepatotoxic agent 0
            thioacetamide 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
                                              acetamides 0
                                                acetamide 0
                                                  thioacetamide 0
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