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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:melophlin R
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Accession:CHEBI:66693 term browser browse the term
Definition:A member of the class of pyrrolidin-2-ones that is 1,5-dimethylpyrrolidine-2,4-dione substituted by a 1-hydroxy-12-methyltetradecylidene moiety at position 3. Isolated from the marine sponge Melophlus sarasinorum and other species of genus Melophlus, it exhibits cytotoxicity against murine leukemia cell line.
Synonyms:exact_synonym: (3Z)-3-(1-hydroxy-12-methyltetradecylidene)-1,5-dimethylpyrrolidine-2,4-dione
 related_synonym: Formula=C21H37NO3;   InChI=1S/C21H37NO3/c1-5-16(2)14-12-10-8-6-7-9-11-13-15-18(23)19-20(24)17(3)22(4)21(19)25/h16-17,23H,5-15H2,1-4H3/b19-18-;   InChIKey=QDDWPSIPKTZOEU-HNENSFHCSA-N;   SMILES=CCC(C)CCCCCCCCCC\\C(O)=C1/C(=O)C(C)N(C)C1=O
 xref: Chemspider:24715723;   PMID:16755057;   Reaxys:10382681

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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            melophlin R 0
Path 2
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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
                                              lactam 0
                                                gamma-lactam 0
                                                  pyrrolidin-2-ones 0
                                                    melophlin R 0
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