more general categories    
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03. Biological Effects of Specific Chemicals   
03. Biological Effects of Specific Chemicals 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
  locoracemoside B [CHEBI:66588] (1) 06. Name of Biological Source of Chemical   
06. Name of Biological Source of Chemical 
 
 
 
 
 
 
  Symplocos racemosa (2) 07. Part of Biological Source of Chemical   
07. Part of Biological Source of Chemical 
 
 
 
 
 
  stem epidermis [PO:0025178] (134) 08. Chemical Category   
08. Chemical Category 
 
 
 
 
 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
  locoracemoside B [CHEBI:66588] (1) 
 
 
 
 
  locoracemoside B [CHEBI:66588] (1) ChEBI Compound Accession Identifier :  [CHEBI:66588] 
ChEBI Compound Description :  An O-acyl carbohydrate consisting of 6-O-beta-D-glucopyranuronosyl-beta-D-glucopyranose attached to a 4-methoxybenzyl and a benzoyl group at positions 1 and 3 respectively. Isolated from Symplocos racemosa, it exhibits inhibitory activity against chymotrypsin. 
ChEBI Compound Identification Number :  66588 
ChEBI InChI Value :  InChI=1S/C27H32O14/c1-36-15-9-7-13(8-10-15)11-37-27-21(32)22(40-25(35)14-5-3-2-4-6-14)17(28)16(39-27)12-38-26-20(31)18(29)19(30)23(41-26)24(33)34/h2-10,16-23,26-32H,11-12H2,1H3,(H,33,34)/t16-,17-,18+,19+,20-,21-,22+,23+,26-,27-/m1/s1 
ChEBI InChIKey Value :  VHIOJRIABYFBNA-LRYVTLDSSA-N 
ChEBI Compound Name :  locoracemoside B 
ChEBI SMILES Value :  COc1ccc(CO[C@@H]2O[C@H](CO[C@@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)C(O)=O)[C@@H](O)[C@H](OC(=O)c3ccccc3)[C@H]2O)cc1 
ChEBI Substance ID :  160710023 
ChEBI URL :  ChEBI:66588  
ChemSpider ID :  28540420 
Ontomatica Chemical Accession Key (OnChAKey) :  VHIOJRIABYFBNA_LRYVTLDSSA_N_000_000000 
PubChem Compound ID :  24850616