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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:piperlactam S
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Accession:CHEBI:132657 term browser browse the term
Definition:An organic heterotetracyclic compound that is dibenzo[cd,f]indol-4(5H)-one carrying two methoxy substituents at positions 1 and 5 as well as a hydroxy substituent at position 2.
Synonyms:exact_synonym: 2-hydroxy-1,5-dimethoxydibenzo[cd,f]indol-4(5H)-one
 related_synonym: Formula=C17H13NO4;   InChI=1S/C17H13NO4/c1-21-16-13(19)8-11-14-12(18(22-2)17(11)20)7-9-5-3-4-6-10(9)15(14)16/h3-8,19H,1-2H3;   InChIKey=LHSDJNRAZBFFLF-UHFFFAOYSA-N;   SMILES=O(C=1C2=C3C(=CC=4C2=CC=CC4)N(C(C3=CC1O)=O)OC)C
 xref: PMID:11040054;   PMID:12498929;   PMID:12567271;   PMID:12567272;   PMID:16724856;   Reaxys:7651039


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  CHEBI ontology 0
    role 0
      chemical role 0
        antioxidant 0
          piperlactam S 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
                                              lactam 0
                                                gamma-lactam 0
                                                  piperlactam S 0
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