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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:Leu-Leu-Tyr
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Accession:CHEBI:6415 term browser browse the term
Definition:A tripeptide composed of L-leucine, L-leucine and L-tyrosine joined in sequence by peptide linkages.
Synonyms:exact_synonym: L-leucyl-L-leucyl-L-tyrosine
 related_synonym: (2S)-2-{[(2S)-2-{[(2S)-2-amino-4-methylpentanoyl]amino}-4-methylpentanoyl]amino}-3-(4-hydroxyphenyl)propanoic acid;   Formula=C21H33N3O5;   InChI=1S/C21H33N3O5/c1-12(2)9-16(22)19(26)23-17(10-13(3)4)20(27)24-18(21(28)29)11-14-5-7-15(25)8-6-14/h5-8,12-13,16-18,25H,9-11,22H2,1-4H3,(H,23,26)(H,24,27)(H,28,29)/t16-,17-,18-/m0/s1;   InChIKey=UCNNZELZXFXXJQ-BZSNNMDCSA-N;   L-L-Y;   L-leu-L-leu-L-tyr;   L-tyrosine, N-(N-L-leucyl-L-leucyl)-;   LLY;   SMILES=N(C([C@@H](NC([C@@H](N)CC(C)C)=O)CC(C)C)=O)[C@H](C(=O)O)CC1=CC=C(C=C1)O;   leucyl-leucyl-tyrosine
 xref: CAS:20368-24-5;   KEGG:C11331;   PMID:12526669;   Reaxys:6352510


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  CHEBI ontology 0
    role 0
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        pharmaceutical 0
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              L-tyrosine 0
                Leu-Leu-Tyr 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
                            heteroorganic entity 0
                              organochalcogen compound 0
                                organooxygen compound 0
                                  carbon oxoacid 0
                                    carboxylic acid 0
                                      carboacyl group 0
                                        univalent carboacyl group 0
                                          formyl group 0
                                            aldehyde 0
                                              amino aldehyde 0
                                                L-tyrosinal 0
                                                  L-tyrosine 0
                                                    Leu-Leu-Tyr 0
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