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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:mandelamide
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Accession:CHEBI:136824 term browser browse the term
Definition:A monocarboxylic acid amide that is phenylacetamide in which one of the benzylic hydrogens has been replaced by a hydroxy group.
Synonyms:exact_synonym: 2-hydroxy-2-phenylacetamide
 related_synonym: Formula=C8H9NO2;   InChI=1S/C8H9NO2/c9-8(11)7(10)6-4-2-1-3-5-6/h1-5,7,10H,(H2,9,11);   InChIKey=MAGPZHKLEZXLNU-UHFFFAOYSA-N;   SMILES=C(N)(=O)C(O)C1=CC=CC=C1
 xref: CAS:4410-31-5;   Reaxys:2208677

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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      biological role 0
        poison 0
          toxin 0
            phenylacetic acid 0
              mandelamide 0
                (R)-mandelamide 0
                (S)-mandelamide 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
                                                mandelamide 0
                                                  (R)-mandelamide 0
                                                  (S)-mandelamide 0
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