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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:N-trans-cinnamoyltyramine
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Accession:CHEBI:177872 term browser browse the term
Definition:A member of the class of cinnamamides that is tyramine substituted by a (1E)-3-oxo-1-phenylprop-1-en-3-yl group at the nitrogen atom. It is found in rice and exhibits an allelopathic effect to suppress the growth of weeds.
Synonyms:exact_synonym: (2E)-N-[2-(4-hydroxyphenyl)ethyl]-3-phenylprop-2-enamide
 related_synonym: (2E)-N-[2-(4-hydroxyphenyl)ethyl]-3-phenyl-2-propenamide;   (E)-N-[2-(4-hydroxyphenyl)ethyl]-3-phenyl-2-propenamide;   Formula=C17H17NO2;   InChI=1S/C17H17NO2/c19-16-9-6-15(7-10-16)12-13-18-17(20)11-8-14-4-2-1-3-5-14/h1-11,19H,12-13H2,(H,18,20)/b11-8+;   InChIKey=KGOYCHSKGXJDND-DHZHZOJOSA-N;   N-cinnamoyltyramine;   SMILES=OC1=CC=C(CCNC(=O)\\C=C\\C2=CC=CC=C2)C=C1;   cinnamoyltyramine;   trans-cinnamoyl-p-hydroxybenzenethylamine
 xref: CAS:103188-44-9;   Chemspider:4475103;   KNApSAcK:C00027156;   MetaCyc:CPD-8941;   PMID:12579800;   PMID:14643446;   PMID:17319684;   PMID:21128731;   PMID:25212867;   PMID:26132274;   PMID:26690131;   PMID:29424281;   PMID:32495600

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          N-trans-cinnamoyltyramine 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
                                          carbamoyl group 0
                                            carboxamide 0
                                              alpha,beta-unsaturated carboxylic acid amide 0
                                                enamide 0
                                                  cinnamamides 0
                                                    N-trans-cinnamoyltyramine 0
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