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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:benzamidoxime
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Accession:CHEBI:83354 term browser browse the term
Definition:A member of the class of amidoximes obtained by formal condensation of the carbonyl group of benzamide with hydroxylamine.
Synonyms:related_synonym: Formula=C7H8N2O;   InChI=1S/C7H8N2O/c8-7(9-10)6-4-2-1-3-5-6/h1-5,10H,(H2,8,9);   InChIKey=MXOQNVMDKHLYCZ-UHFFFAOYSA-N;   N-Hydroxybenzamidine;   N-hydroxybenzenecarboximidamide;   SMILES=NC(=NO)c1ccccc1;   benzamide oxime;   benzohydroxamamide;   phenylhydroxamidine
 xref: CAS:613-92-3
 xref_mesh: MESH:C053561
 xref: PMID:15788365;   PMID:21203183;   PMID:21450516;   PMID:24035094;   PMID:24423752;   PMID:2783015;   PMID:3045129;   PMID:3630202;   PMID:8267515;   Reaxys:606795

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Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      biological role 0
        aetiopathogenetic role 0
          genotoxin 0
            benzamidoxime 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
                                                arenecarboxamide 0
                                                  benzamides 0
                                                    benzamide 0
                                                      benzamidoxime 0
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