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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:pipercallosidine
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Accession:CHEBI:69688 term browser browse the term
Definition:An enamide that is (2E)-N-isobutylhept-2-enamide which is substituted at position 7 by a 3,4-methylenedioxyphenyl group. A natural product found in Piper sarmentosum.
Synonyms:exact_synonym: (2E)-7-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)hept-2-enamide
 related_synonym: Formula=C18H25NO3;   InChI=1S/C18H25NO3/c1-14(2)12-19-18(20)8-6-4-3-5-7-15-9-10-16-17(11-15)22-13-21-16/h6,8-11,14H,3-5,7,12-13H2,1-2H3,(H,19,20)/b8-6+;   InChIKey=PWLZXPUSJOUTMB-SOFGYWHQSA-N;   SMILES=C(/C=C/CCCCC=1C=C2C(=CC1)OCO2)(NCC(C)C)=O
 xref: PMID:21158422;   PMID:21973101;   Reaxys:5587742


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Path 1
Term Annotations click to browse term
  CHEBI ontology 5163
    role 5130
      biological role 5130
        biochemical role 5053
          metabolite 5041
            pipercallosidine 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 5163
    subatomic particle 5154
      composite particle 5154
        hadron 5154
          baryon 5154
            nucleon 5154
              atomic nucleus 5154
                atom 5154
                  main group element atom 5126
                    p-block element atom 5123
                      carbon group element atom 5041
                        carbon atom 5040
                          organic molecular entity 5040
                            heteroorganic entity 4884
                              organochalcogen compound 4838
                                organooxygen compound 4802
                                  carbon oxoacid 393
                                    carboxylic acid 389
                                      carboacyl group 211
                                        univalent carboacyl group 211
                                          carbamoyl group 208
                                            carboxamide 208
                                              alpha,beta-unsaturated carboxylic acid amide 15
                                                enamide 15
                                                  pipercallosidine 0
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