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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:Lucyoside R
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Accession:CHEBI:172793 term browser browse the term
Synonyms:exact_synonym: (3S,4aR,6aR,6aS,6bR,9R,10R,11R,12aR,14bR)-3,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
 related_synonym: Formula=C36H58O11;   InChI=1S/C36H58O11/c1-31(2)13-19-18-7-8-23-32(3)14-20(39)28(47-29-27(43)26(42)25(41)21(16-37)46-29)33(4,17-38)22(32)9-10-35(23,6)34(18,5)11-12-36(19,30(44)45)15-24(31)40/h7,19-29,37-43H,8-17H2,1-6H3,(H,44,45)/t19-,20-,21-,22?,23-,24+,25-,26+,27-,28+,29+,32+,33+,34-,35-,36-/m1/s1;   InChIKey=XARTTWLFBGJXMU-WOQWDUHQSA-N;   SMILES=O([C@@H]1[C@](C2[C@@]([C@@]3([C@]([C@]4(C([C@@]5([C@@](CC4)(C[C@H](O)C(C5)(C)C)C(O)=O)[H])=CC3)C)(CC2)C)[H])(C[C@H]1O)C)(CO)C)[C@@H]6O[C@@H]([C@@H](O)[C@H](O)[C@H]6O)CO
 xref: CAS:206270-86-2;   Chemspider:2340713

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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            saponin 0
              triterpenoid saponin 0
                Lucyoside R 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
                                  carbohydrates and carbohydrate derivatives 0
                                    carbohydrate 0
                                      carbohydrate derivative 0
                                        glycosyl compound 0
                                          glycoside 0
                                            saponin 0
                                              triterpenoid saponin 0
                                                Lucyoside R 0
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