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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:Scorpioidin
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Accession:CHEBI:9060 term browser browse the term
Definition:A germacranolide that has formula C16H20O4.
Synonyms:related_synonym: Formula=C16H20O4;   InChI=1S/C16H20O4/c1-10-5-4-6-12(16(18)19-3)7-8-13-11(2)15(17)20-14(13)9-10/h5,7,13-14H,2,4,6,8-9H2,1,3H3/b10-5+,12-7-/t13-,14+/m1/s1;   InChIKey=OXZSJXCNOUZXAQ-SOVPUBKQSA-N;   SMILES=COC(=O)C1=C\\C[C@H]2[C@H](C\\C(C)=C\\CC\\1)OC(=O)C2=C
 xref: CAS:76045-40-4;   KEGG:C09548;   KNApSAcK:C00003367


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Term Annotations click to browse term
  CHEBI ontology 0
    chemical entity 0
      atom 0
        nonmetal atom 0
          carbon atom 0
            organic molecular entity 0
              isoprenoid 0
                terpene 0
                  sesquiterpene 0
                    germacrane 0
                      germacranolide 0
                        Scorpioidin 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
                                  ester 0
                                    carboxylic ester 0
                                      lactone 0
                                        terpene lactone 0
                                          sesquiterpene lactone 0
                                            germacranolide 0
                                              Scorpioidin 0
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