more general categories    
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03. Biological Effects of Specific Chemicals   
03. Biological Effects of Specific Chemicals 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 05. Industrial Uses   
05. Industrial Uses 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (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)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) 
 
 
 
 
 
  (2S)-2'-methoxykurarinone [CHEBI:66151] (1) ChEBI Compound Accession Identifier :  [CHEBI:66151] 
ChEBI Compound Description :  A dimethoxyflavanone that is (2S)-(-)-kurarinone in which the hydroxy group at position 2' is replaced by a methoxy group. Isolated from the roots of Sophora flavescens, it exhibits cytotoxicity against human myeloid leukemia HL-60 cells. 
ChEBI Compound Identification Number :  66151 
ChEBI InChI Value :  InChI=1S/C27H32O6/c1-15(2)7-8-17(16(3)4)11-20-21(29)13-25(32-6)26-22(30)14-24(33-27(20)26)19-10-9-18(28)12-23(19)31-5/h7,9-10,12-13,17,24,28-29H,3,8,11,14H2,1-2,4-6H3/t17-,24+/m1/s1 
ChEBI InChIKey Value :  KTAQQSUPNZAWEY-OSPHWJPCSA-N 
ChEBI Compound Name :  (2S)-2'-methoxykurarinone 
ChEBI SMILES Value :  COc1cc(O)ccc1[C@@H]1CC(=O)c2c(OC)cc(O)c(C[C@@H](CC=C(C)C)C(C)=C)c2O1 
ChEBI Substance ID :  160710045 
ChEBI URL :  ChEBI:66151  
ChemSpider ID :  10155208 
Ontomatica Chemical Accession Key (OnChAKey) :  KTAQQSUPNZAWEY_OSPHWJPCSA_N_000_000000 
PubChem Compound ID :  11982641