NP-MRD: Showing NP-Card for [3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate (NP0261762)

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Record Information

Version

2.0

Created at

2022-09-08 04:17:43 UTC

Updated at

2022-09-08 04:17:43 UTC

NP-MRD ID

NP0261762

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate

Description

[3-(Benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. [3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate is found in Polygala fallax. Based on a literature review very few articles have been published on [3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082206172D          

 62 67  0  0  0  0            999 V2000
    1.0235   -4.7739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1950   -3.9669    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5820   -3.4149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2027   -3.6698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8158   -3.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6004   -3.3727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7719   -4.1797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5565   -4.4346    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1696   -3.8826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7281   -5.2416    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5127   -5.4965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7676   -6.2812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2827   -6.9486    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5926   -6.2812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0775   -6.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8980   -6.8624    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.4101   -4.2842    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.6849   -2.1798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.5398    0.6693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7148    0.6779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2949   -0.0322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2100   -2.1539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8051   -1.4351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0527    0.0680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6658   -0.4841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4504   -0.2291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4943   -1.2910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1073   -1.8431    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
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 29 34  1  0  0  0  0
 24 35  1  0  0  0  0
 35 36  1  0  0  0  0
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 22 47  1  0  0  0  0
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 49 50  1  0  0  0  0
 50 51  2  0  0  0  0
  3 51  1  0  0  0  0
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 55 56  1  0  0  0  0
 55 57  1  0  0  0  0
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 59 60  1  0  0  0  0
 59 61  1  0  0  0  0
 53 61  1  0  0  0  0
 61 62  1  0  0  0  0
M  END

     RDKit          3D

110115  0  0  0  0  0  0  0  0999 V2000
   -5.0360   -1.3577    2.2304 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1785   -1.2061    1.4148 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0553   -0.6951    0.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8297   -0.3237   -0.3348 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6549    0.1957   -1.5914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4458    0.7305   -2.1537 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3986    1.2221   -1.6253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9770    1.4618   -0.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5371    1.2685    0.7931 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6730    2.0343   -0.1252 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1589    2.3118    1.1677 C   0  0  2  0  0  0  0  0  0  0  0  0
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  -12.0615    0.5198    1.7625 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


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M  END
> <DATABASE_ID>
NP0261762

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C=CC(=O)OC2C(O)C(CO)OC2(CO)OC2OC(COC(=O)C3=CC=CC=C3)C(OC(=O)C3=CC=CC=C3)C(O)C2O)=CC=C1OC1OC(C)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C42H48O20/c1-21-30(46)32(48)34(50)40(56-21)57-25-15-13-22(17-26(25)54-2)14-16-29(45)59-37-31(47)27(18-43)61-42(37,20-44)62-41-35(51)33(49)36(60-39(53)24-11-7-4-8-12-24)28(58-41)19-55-38(52)23-9-5-3-6-10-23/h3-17,21,27-28,30-37,40-41,43-44,46-51H,18-20H2,1-2H3

> <INCHI_KEY>
MVWFADQKFNMFBG-UHFFFAOYSA-N

> <FORMULA>
C42H48O20

> <MOLECULAR_WEIGHT>
872.826

> <EXACT_MASS>
872.273893946

> <JCHEM_ACCEPTOR_COUNT>
17

> <JCHEM_ATOM_COUNT>
110

> <JCHEM_AVERAGE_POLARIZABILITY>
86.70484433192587

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate

> <JCHEM_LOGP>
1.8132607376666656

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.375937782746565

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.88494275016036

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9814532563443565

> <JCHEM_POLAR_SURFACE_AREA>
296.11999999999995

> <JCHEM_REFRACTIVITY>
207.03059999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       1.911  -8.911   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.231  -7.405   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.086  -6.374   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.378  -6.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.523  -5.820   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.987  -6.296   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.308  -7.802   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.772  -8.278   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -5.917  -7.247   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -5.092  -9.784   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -6.557 -10.260   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -7.033 -11.725   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -6.128 -12.971   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -8.573 -11.725   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -9.478 -12.971   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0     -11.010 -12.810   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -9.049 -10.260   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -7.803  -9.355   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -8.559  -8.013   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0     -10.099  -7.997   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -7.047  -8.013   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -7.831  -6.688   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -9.371  -6.704   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0     -10.155  -5.378   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -11.695  -5.394   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0     -12.451  -6.736   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0     -13.990  -6.752   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0     -14.774  -5.427   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0     -14.746  -8.094   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -13.963  -9.420   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -14.719 -10.761   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -16.258 -10.777   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -17.042  -9.452   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -16.286  -8.110   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -9.399  -4.037   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0     -10.183  -2.711   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0     -11.723  -2.727   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0     -12.479  -4.069   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0     -12.506  -1.402   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -14.046  -1.418   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -14.830  -0.092   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0     -14.074   1.249   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0     -12.534   1.265   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -11.750  -0.060   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -7.859  -4.021   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -7.103  -2.679   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -7.075  -5.346   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -5.535  -5.330   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -1.203  -4.313   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       0.262  -3.838   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       1.406  -4.868   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       2.871  -4.392   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       3.191  -2.886   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0       2.047  -1.855   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0       2.367  -0.349   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       1.223   0.681   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0       3.832   0.127   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0       4.152   1.633   0.000  0.00  0.00           O+0
HETATM   59  C   UNK     0       4.976  -0.904   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0       6.441  -0.428   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0       4.656  -2.410   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0       5.800  -3.440   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   51                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   49                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18                                                       
CONECT   18   17   11   19   21                                             
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22                                                       
CONECT   22   21   23   47                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   35                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   29                                                       
CONECT   35   24   36   45                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   44                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   39                                                       
CONECT   45   35   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   22   48                                                  
CONECT   48   47                                                            
CONECT   49    5   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50    3   52                                                  
CONECT   52   51   53                                                       
CONECT   53   52   54   61                                                  
CONECT   54   53   55                                                       
CONECT   55   54   56   57                                                  
CONECT   56   55                                                            
CONECT   57   55   58   59                                                  
CONECT   58   57                                                            
CONECT   59   57   60   61                                                  
CONECT   60   59                                                            
CONECT   61   59   53   62                                                  
CONECT   62   61                                                            
MASTER        0    0    0    0    0    0    0    0   62    0  134    0
END

View in JSmol

Synonyms

Value	Source
[3-(Benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoic acid	Generator

Chemical Formula

C₄₂H₄₈O₂₀

Average Mass

872.8260 Da

Monoisotopic Mass

872.27389 Da

IUPAC Name

[3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate

Traditional Name

[3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate

CAS Registry Number

Not Available

SMILES

COC1=CC(C=CC(=O)OC2C(O)C(CO)OC2(CO)OC2OC(COC(=O)C3=CC=CC=C3)C(OC(=O)C3=CC=CC=C3)C(O)C2O)=CC=C1OC1OC(C)C(O)C(O)C1O

InChI Identifier

InChI=1S/C42H48O20/c1-21-30(46)32(48)34(50)40(56-21)57-25-15-13-22(17-26(25)54-2)14-16-29(45)59-37-31(47)27(18-43)61-42(37,20-44)62-41-35(51)33(49)36(60-39(53)24-11-7-4-8-12-24)28(58-41)19-55-38(52)23-9-5-3-6-10-23/h3-17,21,27-28,30-37,40-41,43-44,46-51H,18-20H2,1-2H3

InChI Key

MVWFADQKFNMFBG-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Polygala fallax	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
Cinnamic acid ester
Coumaric acid or derivatives
Cinnamic acid or derivatives
O-glycosyl compound
Disaccharide
C-glycosyl compound
Benzoate ester
Tricarboxylic acid or derivatives
Benzoic acid or derivatives
Benzoyl
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
Anisole
Fatty acid ester
Alkyl aryl ether
Ketal
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Oxane
Tetrahydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Carboxylic acid ester
Polyol
Ether
Acetal
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Hydrocarbon derivative
Alcohol
Organic oxide
Carbonyl group
Primary alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.81	ChemAxon
pKa (Strongest Acidic)	11.88	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	17	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	296.12 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	207.03 m³·mol⁻¹	ChemAxon
Polarizability	86.7 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162872404

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate (NP0261762)

MOL for NP0261762 ([3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate)

3D MOL for NP0261762 ([3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate)

3D SDF for NP0261762 ([3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate)

3D-SDF for NP0261762 ([3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate)

PDB for NP0261762 ([3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate)

3D PDB for NP0261762 ([3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate)

SMILES for NP0261762 ([3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate)

INCHI for NP0261762 ([3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate)

Structure for NP0261762 ([3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate)

3D Structure for NP0261762 ([3-(benzoyloxy)-4,5-dihydroxy-6-{[4-hydroxy-2,5-bis(hydroxymethyl)-3-[(3-{3-methoxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]phenyl}prop-2-enoyl)oxy]oxolan-2-yl]oxy}oxan-2-yl]methyl benzoate)