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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:yanuthone F
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Accession:CHEBI:133835 term browser browse the term
Definition:A class I yanuthone that is 7-deacetoxyyanuthone A in which one of the hydrogens of the trans-terminal methyl groups of the sesquiterpenoid side-chain has been replaced by a hydroxy group.
Synonyms:exact_synonym: (1R,5R,6R)-5-hydroxy-1-[(2E,6E,10E)-12-hydroxy-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]-4-methyl-7-oxabicyclo[4.1.0]hept-3-en-2-one
 related_synonym: Formula=C22H32O4;   InChI=1S/C22H32O4/c1-15(8-6-10-17(3)14-23)7-5-9-16(2)11-12-22-19(24)13-18(4)20(25)21(22)26-22/h7,10-11,13,20-21,23,25H,5-6,8-9,12,14H2,1-4H3/b15-7+,16-11+,17-10+/t20-,21-,22+/m1/s1;   InChIKey=QJQOZQGLFNQSKQ-TVXDRXDOSA-N;   SMILES=C/C(=C\\CC\\C(\\C)=C\\C[C@]12C(C=C([C@H]([C@H]1O2)O)C)=O)/CC/C=C(\\C)/CO
 xref: PMID:24684908;   PMID:25293978;   Reaxys:27020140


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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            meroterpenoid 0
              yanuthones 0
                class I yanuthone 0
                  yanuthone F 0
                    yanuthone G 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
                                  carbonyl compound 0
                                    ketone 0
                                      cyclic ketone 0
                                        alicyclic ketone 0
                                          cyclohexenones 0
                                            yanuthones 0
                                              class I yanuthone 0
                                                7-deacetoxyyanuthone A 0
                                                  yanuthone F 0
                                                    yanuthone G 0
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