more general categories    
information about this item 
03. Biological Effects of Specific Chemicals   
03. Biological Effects of Specific Chemicals 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 05. Industrial Uses   
05. Industrial Uses 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 06. Name of Biological Source of Chemical   
06. Name of Biological Source of Chemical 
 
 
 
 
 
 
 
  Sophora flavescens (7) 07. Part of Biological Source of Chemical   
07. Part of Biological Source of Chemical 
 
 
 
 
  root [PO:0009005] (486) 08. Chemical Category   
08. Chemical Category 
 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
 
 
 
 
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  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
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  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
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  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
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  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
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  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
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  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
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  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
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  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
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  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
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  (2S)-(-)-kurarinone [CHEBI:66150] (1) 
 
 
 
 
 
  (2S)-(-)-kurarinone [CHEBI:66150] (1) ChEBI Compound Accession Identifier :  [CHEBI:66150] 
ChEBI Compound Description :  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. 
ChEBI Compound Identification Number :  66150 
ChEBI InChI Value :  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 
ChEBI InChIKey Value :  LTTQKYMNTNISSZ-MWTRTKDXSA-N 
ChEBI Compound Name :  (2S)-(-)-kurarinone 
ChEBI SMILES Value :  COc1cc(O)c(C[C@@H](CC=C(C)C)C(C)=C)c2O[C@@H](CC(=O)c12)c1ccc(O)cc1O 
ChEBI Substance ID :  160710094 
ChEBI URL :  ChEBI:66150  
ChemSpider ID :  10155207 
Ontomatica Chemical Accession Key (OnChAKey) :  LTTQKYMNTNISSZ_MWTRTKDXSA_N_000_000000 
PubChem Compound ID :  11982640