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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:Aciculatin
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Accession:CHEBI:179276 term browser browse the term
Synonyms:exact_synonym: 8-[(2S,4S,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one
 related_synonym: Formula=C22H22O8;   InChI=1S/C22H22O8/c1-10-21(27)15(26)9-18(29-10)20-17(28-2)8-14(25)19-13(24)7-16(30-22(19)20)11-3-5-12(23)6-4-11/h3-8,10,15,18,21,23,25-27H,9H2,1-2H3/t10-,15+,18+,21-/m1/s1;   InChIKey=RUTGHCUXABPJTJ-VAXHSPNUSA-N;   SMILES=O1[C@@](C[C@H](O)[C@H](O)[C@H]1C)(C=2C=3OC(=CC(=O)C3C(O)=CC2OC)C4=CC=C(O)C=C4)[H]
 xref: CAS:134044-97-6;   Chemspider:116365
 xref_mesh: MESH:C074400


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Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 5152
    chemical entity 5152
      atom 5143
        nonmetal atom 5109
          oxygen atom 4979
            oxygen molecular entity 4979
              flavonoids 43
                Aciculatin 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 5152
    subatomic particle 5143
      composite particle 5143
        hadron 5143
          baryon 5143
            nucleon 5143
              atomic nucleus 5143
                atom 5143
                  main group element atom 5116
                    p-block element atom 5113
                      carbon group element atom 5031
                        carbon atom 5030
                          organic molecular entity 5030
                            heteroorganic entity 4875
                              organochalcogen compound 4829
                                organooxygen compound 4793
                                  carbohydrates and carbohydrate derivatives 123
                                    carbohydrate 123
                                      carbohydrate derivative 112
                                        glycosyl compound 50
                                          C-glycosyl compound 0
                                            Aciculatin 0
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