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:Pro-Lys-Pro
go back to main search page
Accession:CHEBI:162485 term browser browse the term
Synonyms:exact_synonym: (2R)-1-[(2S)-6-amino-2-[[(2S)-pyrrolidine-2-carbonyl]amino]hexanoyl]pyrrolidine-2-carboxylic acid
 related_synonym: Formula=C16H28N4O4;   InChI=1S/C16H28N4O4/c17-8-2-1-5-12(19-14(21)11-6-3-9-18-11)15(22)20-10-4-7-13(20)16(23)24/h11-13,18H,1-10,17H2,(H,19,21)(H,23,24)/t11-,12-,13+/m0/s1;   InChIKey=ULWBBFKQBDNGOY-RWMBFGLXSA-N;   SMILES=O=C(N1[C@H](CCC1)C(O)=O)[C@@H](NC(=O)[C@H]2NCCC2)CCCCN


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
          amino-acid residue 0
            peptide 0
              Pro-Lys-Pro 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
                                              peptide 0
                                                Pro-Lys-Pro 0
paths to the root