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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:linuron
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Accession:CHEBI:6482 term browser browse the term
Definition:A member of the class of phenylureas that is N-methyl urea substituted by a methoxy group at position 1 and a 3,4-dichlorophenyl group at position 3.
Synonyms:related_synonym: 1-Methoxy-1-methyl-3-(3,4-dichlorophenyl)urea;   3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea;   Formula=C9H10Cl2N2O2;   InChI=1S/C9H10Cl2N2O2/c1-13(15-2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14);   InChIKey=XKJMBINCVNINCA-UHFFFAOYSA-N;   N'-(3,4-dichlorophenyl)-N-methoxy-N-methyl Urea;   SMILES=CON(C)C(=O)Nc1ccc(Cl)c(Cl)c1
 xref: CAS:330-55-2;   KEGG:C11007
 xref_mesh: MESH:D008044
 xref: PMID:23586778;   PMID:24410802;   PMID:25238184;   PPDB:419;   Pesticides:linuron;   Reaxys:2128725


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Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    role 0
      application 0
        agrochemical 0
          linuron 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
                                                urea 0
                                                  ureas 0
                                                    phenylureas 0
                                                      linuron 0
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