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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:rebaudioside B(1-)
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Accession:CHEBI:145013 term browser browse the term
Synonyms:related_synonym: Formula=C38H59O18;   InChI=1S/C38H60O18/c1-16-11-37-9-5-20-35(2,7-4-8-36(20,3)34(49)50)21(37)6-10-38(16,15-37)56-33-30(55-32-28(48)26(46)23(43)18(13-40)52-32)29(24(44)19(14-41)53-33)54-31-27(47)25(45)22(42)17(12-39)51-31/h17-33,39-48H,1,4-15H2,2-3H3,(H,49,50)/p-1/t17-,18-,19-,20+,21+,22-,23-,24-,25+,26+,27-,28-,29+,30-,31+,32+,33+,35-,36-,37-,38+/m1/s1;   InChIKey=DRSKVOAJKLUMCL-MMUIXFKXSA-M;   SMILES=[O-]C([C@]1([C@@]2([C@]([C@]3([C@]4(C[C@@](O[C@H]5[C@H](O[C@@H]6O[C@@H]([C@@H](O)[C@@H]([C@H]6O)O)CO)[C@H]([C@H](O)[C@H](O5)CO)O[C@@H]7O[C@@H]([C@@H](O)[C@@H]([C@H]7O)O)CO)(CC3)C(C4)=C)CC2)[H])(CCC1)C)[H])C)=O;   rebaudioside B
 xref: MetaCyc:CPD-14507;   PMID:15610349;   PMID:31324778


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Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 221
    role 221
      biological role 221
        epitope 18
          beta-D-glucose 1
            beta-D-glucoside 1
              rebaudioside B(1-) 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 221
    subatomic particle 221
      composite particle 221
        hadron 221
          baryon 221
            nucleon 221
              atomic nucleus 221
                atom 221
                  main group element atom 214
                    p-block element atom 214
                      carbon group element atom 203
                        carbon atom 202
                          organic molecular entity 202
                            heteroorganic entity 196
                              organochalcogen compound 165
                                organooxygen compound 164
                                  carbohydrates and carbohydrate derivatives 38
                                    carbohydrate 38
                                      monosaccharide 6
                                        aldose 2
                                          aldohexose 2
                                            glucose 2
                                              D-glucose 2
                                                D-glucopyranose 1
                                                  beta-D-glucose 1
                                                    beta-D-glucoside 1
                                                      rebaudioside B(1-) 0
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