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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:kaempferol 7-O-(2-E-p-coumaroyl-alpha-L-rhamnopyranoside)
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Accession:CHEBI:66134 term browser browse the term
Definition:A glycosyloxyflavone that consists of kaempferol attached to a 2-E-p-coumaroyl-alpha-L-rhamnopyranosyl moiety at position 7 via a glycosidic linkage. Isolated from the flowers and fruits of Tetrapanax papyriferus, it exhibits antineoplastic activity.
Synonyms:exact_synonym: 3,5-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl 6-deoxy-2-O-[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]-alpha-L-mannopyranoside
 related_synonym: Formula=C30H26O12;   InChI=1S/C30H26O12/c1-14-24(35)26(37)29(42-22(34)11-4-15-2-7-17(31)8-3-15)30(39-14)40-19-12-20(33)23-21(13-19)41-28(27(38)25(23)36)16-5-9-18(32)10-6-16/h2-14,24,26,29-33,35,37-38H,1H3/b11-4+/t14-,24-,26+,29+,30-/m0/s1;   InChIKey=XUUODWXANHZAFB-OKOXDJDNSA-N;   SMILES=C[C@@H]1O[C@@H](Oc2cc(O)c3c(c2)oc(-c2ccc(O)cc2)c(O)c3=O)[C@H](OC(=O)\\C=C\\c2ccc(O)cc2)[C@H](O)[C@H]1O
 xref: PMID:16378372;   Reaxys:15775333

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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            kaempferol 7-O-(2-E-p-coumaroyl-alpha-L-rhamnopyranoside) 0
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  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
                                  carbon oxoacid 0
                                    carboxylic acid 0
                                      monocarboxylic acid 0
                                        alpha,beta-unsaturated monocarboxylic acid 0
                                          cinnamic acids 0
                                            hydroxycinnamic acid 0
                                              monohydroxycinnamic acid 0
                                                coumaric acid 0
                                                  4-coumaric acid 0
                                                    trans-4-coumaric acid 0
                                                      kaempferol 7-O-(2-E-p-coumaroyl-alpha-L-rhamnopyranoside) 0
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