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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:tebutam
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Accession:CHEBI:82043 term browser browse the term
Definition:A monocarboxylic acid amide that is propanamide substituted by a benzyl and an isopropyl group at the nitrogen atom and two methyl groups at position 2. It is an agrochemical used as a herbicide.
Synonyms:exact_synonym: N-benzyl-2,2-dimethyl-N-(propan-2-yl)propanamide
 related_synonym: Butam;   Formula=C15H23NO;   InChI=1S/C15H23NO/c1-12(2)16(14(17)15(3,4)5)11-13-9-7-6-8-10-13/h6-10,12H,11H2,1-5H3;   InChIKey=RJKCKKDSSSRYCB-UHFFFAOYSA-N;   N-Benzyl-N-isopropyltrimethylacetamide;   N-benzyl-N-isopropylpivalamide;   SMILES=CC(C)N(Cc1ccccc1)C(=O)C(C)(C)C
 xref: AGR:IND86014658;   CAS:35256-85-0;   KEGG:C18896;   PPDB:613;   Patent:EP0110660;   Patent:US4456472;   Pesticides:tebutam

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Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      application 0
        agrochemical 0
          tebutam 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
                                                tebutam 0
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