Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

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:carbamoyl group
go back to main search page
Accession:CHEBI:23004 term browser browse the term
Definition:The univalent carboacyl group formed by loss of -OH from the carboxy group of carbamic acid.
Synonyms:exact_synonym: carbamoyl
 related_synonym: -C(O)NH2;   -CONH2;   Formula=CH2NO;   SMILES=*C(N)=O;   aminocarbonyl;   carbamyl;   carbamyl group;   carboxamide
 xref: PMID:24168430


GViewer not supported for the selected species.

show annotations for term's descendants           Sort by:

Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    chemical entity 0
      group 0
        organic group 0
          acyl group 0
            carboacyl group 0
              univalent carboacyl group 0
                carbamoyl group 0
                  N-methylcarbamoyl group 0
                  carboxamide + 0
                  carnitinamide + 0
                  oxcarbazepine 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
                                            N-methylcarbamoyl group 0
                                            carboxamide + 0
                                            carnitinamide + 0
                                            oxcarbazepine 0
paths to the root