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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:imidocarb
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Accession:CHEBI:51804 term browser browse the term
Definition:An urea that has formula C19H20N6O.
Synonyms:exact_synonym: 1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea
 related_synonym: 1,3-Bis(3-(2-imidazolin-2-yl)phenyl)harnstoff;   1,3-bis(3-(2-imidazolin-2-yl)phenyl)urea;   Formula=C19H20N6O;   InChI=1S/C19H20N6O/c26-19(24-15-5-1-3-13(11-15)17-20-7-8-21-17)25-16-6-2-4-14(12-16)18-22-9-10-23-18/h1-6,11-12H,7-10H2,(H,20,21)(H,22,23)(H2,24,25,26);   InChIKey=SCEVFJUWLLRELN-UHFFFAOYSA-N;   N,N'-bis(3-(4,5-dihydro-1H-imidazol-2-yl)phenyl)urea;   SMILES=O=C(Nc1cccc(c1)C1=NCCN1)Nc1cccc(c1)C1=NCCN1;   imidocarbe;   imidocarbo;   imidocarbum
 xref: Beilstein:964732;   CAS:27885-92-3;   Patent:GB1007334;   Patent:US3338917


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  CHEBI ontology 0
    role 0
      biological role 0
        antimicrobial agent 0
          antimicrobial drug 0
            antiprotozoal drug 0
              imidocarb 0
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  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
                            organic group 0
                              organic divalent group 0
                                organodiyl group 0
                                  carbonyl group 0
                                    carbonyl compound 0
                                      carboxylic acid 0
                                        carboacyl group 0
                                          univalent carboacyl group 0
                                            carbamoyl group 0
                                              carboxamide 0
                                                monocarboxylic acid amide 0
                                                  urea 0
                                                    ureas 0
                                                      imidocarb 0
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