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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:decursinol
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Accession:CHEBI:4354 term browser browse the term
Definition:An organic heterotricyclic compound that is 7,8-dihydro-2H,6H-pyrano[3,2-g]chromen-2-one substituted by a beta-hydroxy group at position 7 and two methyl groups at position 8. It is isolated from the roots of Angelica gigas and has been found to possess significant inhibitory activity against acetylcholinesterase enzyme (EC 3.1.1.7).
Synonyms:exact_synonym: (7S)-7-hydroxy-8,8-dimethyl-7,8-dihydro-2H,6H-pyrano[3,2-g]chromen-2-one
 related_synonym: (S)-(+)-decursinol;   Formula=C14H14O4;   InChI=1S/C14H14O4/c1-14(2)12(15)6-9-5-8-3-4-13(16)17-10(8)7-11(9)18-14/h3-5,7,12,15H,6H2,1-2H3/t12-/m0/s1;   InChIKey=BGXFQDFSVDZUIW-LBPRGKRZSA-N;   SMILES=CC1(C)Oc2cc3oc(=O)ccc3cc2C[C@@H]1O
 alt_id: CHEBI:65731
 xref: CAS:23458-02-8;   KEGG:C09259;   KNApSAcK:C00002466;   PMID:11374978;   PMID:19557373;   PMID:21170925;   PMID:21657833;   PMID:22116603;   Reaxys:1621844

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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            decursinol 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
                                        delta-lactone 0
                                          decursinol 0
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