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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:fenhexamid
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Accession:CHEBI:81853 term browser browse the term
Definition:An aromatic amide resulting from the formal condensation of the carboxy group of 1-methylcyclohexanecarboxylic acid with the amino group of 4-amino-2,3-dichlorophenol.
Synonyms:exact_synonym: N-(2,3-dichloro-4-hydroxyphenyl)-1-methylcyclohexanecarboxamide
 related_synonym: 2',3'-dichloro-4'-hydroxy-1-methylcyclohexanecarboxanilide;   Formula=C14H17Cl2NO2;   InChI=1S/C14H17Cl2NO2/c1-14(7-3-2-4-8-14)13(19)17-9-5-6-10(18)12(16)11(9)15/h5-6,18H,2-4,7-8H2,1H3,(H,17,19);   InChIKey=VDLGAVXLJYLFDH-UHFFFAOYSA-N;   KBR 2738;   N-(2,3-dichloro-4-hydroxyphenyl)-1-methylcyclohexane-1-carboxamide;   SMILES=CC1(CCCCC1)C(=O)Nc1ccc(O)c(Cl)c1Cl;   Teldor;   fenhexamide
 alt_id: MESH:C451426
 xref: AGR:IND500627165;   CAS:126833-17-8;   KEGG:C18593
 xref_mesh: MESH:C451426
 xref: PMID:17390774;   PMID:19285148;   PMID:22045588;   PMID:23052036;   PMID:23139232;   PPDB:298;   Patent:EP339418;   Patent:US5059623;   Pesticides:fenhexamid;   Reaxys:8996658


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Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      biological role 0
        inhibitor 0
          sterol biosynthesis inhibitor 0
            fenhexamid 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
                                                fenhexamid 0
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