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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:(2S)-(-)-kurarinone
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Accession:CHEBI:66150 term browser browse the term
Definition:A trihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 7, 2' and 4', a lavandulyl group at position 8 and a methoxy group at position 5. Isolated from the roots of Sophora flavescens, it exhibits cytotoxicity against human myeloid leukemia HL-60 cells.
Synonyms:exact_synonym: (2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-8-[(2R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-2,3-dihydro-4H-chromen-4-one
 related_synonym: 7,2',4'-trihydroxy-8-lavandulyl-5-methoxyflavanone;   Formula=C26H30O6;   InChI=1S/C26H30O6/c1-14(2)6-7-16(15(3)4)10-19-21(29)12-24(31-5)25-22(30)13-23(32-26(19)25)18-9-8-17(27)11-20(18)28/h6,8-9,11-12,16,23,27-29H,3,7,10,13H2,1-2,4-5H3/t16-,23+/m1/s1;   InChIKey=LTTQKYMNTNISSZ-MWTRTKDXSA-N;   SMILES=COc1cc(O)c(C[C@@H](CC=C(C)C)C(C)=C)c2O[C@@H](CC(=O)c12)c1ccc(O)cc1O
 xref: KEGG:C17446;   LIPID_MAPS_instance:LMPK12140499;   PMID:10843587;   PMID:21831037;   PMID:22932446;   PMID:23333426;   Patent:CN102018697;   Patent:WO2005095375;   Reaxys:9739392

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  CHEBI ontology 0
    role 0
      biological role 0
        biochemical role 0
          metabolite 0
            (2S)-(-)-kurarinone 0
              (2S)-2'-methoxykurarinone 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
                            organic molecule 0
                              organic cyclic compound 0
                                organic heterocyclic compound 0
                                  oxacycle 0
                                    benzopyran 0
                                      1-benzopyran 0
                                        flavonoid 0
                                          flavans 0
                                            flavanones 0
                                              hydroxyflavanone 0
                                                4'-hydroxyflavanones 0
                                                  (2S)-(-)-kurarinone 0
                                                    (2S)-2'-methoxykurarinone 0
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