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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:5-hydroxy-6,7,3',4',5'-pentamethoxyflavanone 5-O-rhamnoside
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Accession:CHEBI:140140 term browser browse the term
Synonyms:related_synonym: Formula=C26H32O12;   InChI=1S/C26H32O12/c1-11-20(28)21(29)22(30)26(36-11)38-25-19-13(27)9-14(37-15(19)10-18(33-4)24(25)35-6)12-7-16(31-2)23(34-5)17(8-12)32-3/h7-8,10-11,14,20-22,26,28-30H,9H2,1-6H3/t11-,14?,20-,21+,22+,26-/m0/s1;   InChIKey=BHSHENYSLDZJHG-SIVMCWDOSA-N;   SMILES=C=1(C(=C(C2=C(C1)OC(CC2=O)C3=CC(=C(C(=C3)OC)OC)OC)O[C@H]4[C@@H]([C@@H]([C@H]([C@@H](O4)C)O)O)O)OC)OC
 xref: LIPID_MAPS_instance:LMPK12140634


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Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 0
    chemical entity 0
      atom 0
        nonmetal atom 0
          oxygen atom 0
            oxygen molecular entity 0
              flavonoids 0
                5-hydroxy-6,7,3',4',5'-pentamethoxyflavanone 5-O-rhamnoside 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
                                            5-hydroxy-6,7,3',4',5'-pentamethoxyflavanone 5-O-rhamnoside 0
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