NP-MRD: Showing NP-Card for 1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate (NP0232286)

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Record Information

Version

2.0

Created at

2022-09-06 13:28:25 UTC

Updated at

2022-09-06 13:28:25 UTC

NP-MRD ID

NP0232286

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate

Description

1,4-Bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate 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. 1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate is found in Gymnadenia conopsea and Dactylorhiza hatagirea. 1,4-Bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251515502D          

 63 67  0  0  0  0            999 V2000
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   -2.9117   -3.7843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0706   -4.0983    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4019   -4.6932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1941   -5.5489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8815   -6.0700    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9160   -6.7821    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6329   -7.1903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6378   -8.0153    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9905   -3.6099    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
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 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
  7 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 18  1  0  0  0  0
 18 19  1  0  0  0  0
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 20 21  2  0  0  0  0
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 46 63  1  0  0  0  0
M  END

     RDKit          3D

119123  0  0  0  0  0  0  0  0999 V2000
    3.3698   -4.5450    0.6219 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6272   -3.1598    0.5850 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5169   -2.3145   -0.2393 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2923   -3.0506    6.4471 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5827   -2.6766    7.1394 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1533004251515502D          

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M  END
> <DATABASE_ID>
NP0232286

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC(OC1OC(CO)C(O)C(O)C1O)(C(O)C(=O)OCC1=CC=C(OC2OC(CO)C(O)C(O)C2O)C=C1)C(=O)OCC1=CC=C(OC2OC(CO)C(O)C(O)C2O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C40H56O23/c1-17(2)11-40(63-38-33(52)30(49)27(46)24(14-43)62-38,39(55)57-16-19-5-9-21(10-6-19)59-37-32(51)29(48)26(45)23(13-42)61-37)34(53)35(54)56-15-18-3-7-20(8-4-18)58-36-31(50)28(47)25(44)22(12-41)60-36/h3-10,17,22-34,36-38,41-53H,11-16H2,1-2H3

> <INCHI_KEY>
KGCBATGZRGGGQG-UHFFFAOYSA-N

> <FORMULA>
C40H56O23

> <MOLECULAR_WEIGHT>
904.865

> <EXACT_MASS>
904.321238063

> <JCHEM_ACCEPTOR_COUNT>
21

> <JCHEM_ATOM_COUNT>
119

> <JCHEM_AVERAGE_POLARIZABILITY>
88.72439199800989

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,4-bis(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate

> <ALOGPS_LOGP>
-1.00

> <JCHEM_LOGP>
-3.315291975333334

> <ALOGPS_LOGS>
-2.47

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.852555681748493

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.193449668271027

> <JCHEM_PKA_STRONGEST_BASIC>
-3.648395345629174

> <JCHEM_POLAR_SURFACE_AREA>
370.9700000000001

> <JCHEM_REFRACTIVITY>
204.0276

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.04e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,4-bis(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -7.779  -9.413   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.893  -7.772   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.603  -7.189   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.435  -7.064   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.865  -7.650   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -2.617  -8.761   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.229 -10.358   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.512 -11.331   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -3.576 -12.660   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.915 -13.422   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -4.924 -14.962   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -2.247 -13.438   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -2.257 -14.978   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.909 -12.676   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.420 -13.454   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.900 -11.136   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.700 -11.213   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -4.810  -9.034   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.727 -10.174   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -6.403  -9.183   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -7.795  -8.153   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -7.297 -10.636   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -9.063 -10.360   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -10.030 -11.558   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -9.476 -12.995   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -10.443 -14.193   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -11.965 -13.955   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0     -12.932 -15.153   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0     -14.453 -14.915   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0     -15.420 -16.113   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0     -16.942 -15.875   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -17.909 -17.074   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0     -19.430 -16.835   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0     -17.496 -14.438   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0     -19.018 -14.200   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0     -16.529 -13.240   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0     -17.083 -11.803   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0     -15.008 -13.478   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0     -14.040 -12.280   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0     -12.519 -12.518   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -11.552 -11.320   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -3.155  -6.122   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -3.490  -4.566   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      -1.636  -5.673   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      -0.401  -4.727   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       1.087  -5.400   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       1.865  -4.071   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       3.405  -4.080   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       4.167  -5.419   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       5.740  -5.482   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0       6.485  -4.099   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       5.723  -2.761   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       6.501  -1.431   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       5.900   0.076   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       6.213   1.617   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0       8.041  -1.441   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0       9.013  -0.178   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0       8.803  -2.779   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      10.396  -2.795   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0       8.025  -4.108   0.000  0.00  0.00           C+0
HETATM   61  O   UNK     0       8.950  -5.407   0.000  0.00  0.00           O+0
HETATM   62  C   UNK     0       3.389  -6.748   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0       1.849  -6.739   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   18   42                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   16                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    7   17                                                  
CONECT   17   16                                                            
CONECT   18    5   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   41                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   40                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30   38                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   29   39                                                  
CONECT   39   38                                                            
CONECT   40   27   41                                                       
CONECT   41   40   24                                                       
CONECT   42    5   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47   63                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50   62                                                  
CONECT   50   49   51                                                       
CONECT   51   50   52   60                                                  
CONECT   52   51   53                                                       
CONECT   53   52   54   56                                                  
CONECT   54   53   55                                                       
CONECT   55   54                                                            
CONECT   56   53   57   58                                                  
CONECT   57   56                                                            
CONECT   58   56   59   60                                                  
CONECT   59   58                                                            
CONECT   60   58   51   61                                                  
CONECT   61   60                                                            
CONECT   62   49   63                                                       
CONECT   63   62   46                                                       
MASTER        0    0    0    0    0    0    0    0   63    0  134    0
END

View in JSmol

Synonyms

Value	Source
1,4-Bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioic acid	Generator

Chemical Formula

C₄₀H₅₆O₂₃

Average Mass

904.8650 Da

Monoisotopic Mass

904.32124 Da

IUPAC Name

1,4-bis(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate

Traditional Name

1,4-bis(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate

CAS Registry Number

Not Available

SMILES

CC(C)CC(OC1OC(CO)C(O)C(O)C1O)(C(O)C(=O)OCC1=CC=C(OC2OC(CO)C(O)C(O)C2O)C=C1)C(=O)OCC1=CC=C(OC2OC(CO)C(O)C(O)C2O)C=C1

InChI Identifier

InChI=1S/C40H56O23/c1-17(2)11-40(63-38-33(52)30(49)27(46)24(14-43)62-38,39(55)57-16-19-5-9-21(10-6-19)59-37-32(51)29(48)26(45)23(13-42)61-37)34(53)35(54)56-15-18-3-7-20(8-4-18)58-36-31(50)28(47)25(44)22(12-41)60-36/h3-10,17,22-34,36-38,41-53H,11-16H2,1-2H3

InChI Key

KGCBATGZRGGGQG-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
Gymnadenia conopsea	LOTUS Database	35616633
Orchis hatagirea	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
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Disaccharide
O-glycosyl compound
Benzyloxycarbonyl
Phenoxy compound
Phenol ether
Beta-hydroxy acid
Fatty acid ester
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Fatty acyl
Benzenoid
Hydroxy acid
Oxane
Carboxylic acid ester
Secondary alcohol
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Acetal
Polyol
Organic oxide
Alcohol
Carbonyl group
Primary alcohol
Hydrocarbon derivative
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	ALOGPS
logP	-3.3	ChemAxon
logS	-2.5	ALOGPS
pKa (Strongest Acidic)	11.19	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	21	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	370.97 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	204.03 m³·mol⁻¹	ChemAxon
Polarizability	88.72 Å³	ChemAxon
Number of Rings	5	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

11766270

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate (NP0232286)

MOL for NP0232286 (1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate)

3D MOL for NP0232286 (1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate)

3D SDF for NP0232286 (1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate)

3D-SDF for NP0232286 (1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate)

PDB for NP0232286 (1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate)

3D PDB for NP0232286 (1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate)

SMILES for NP0232286 (1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate)

INCHI for NP0232286 (1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate)

Structure for NP0232286 (1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate)

3D Structure for NP0232286 (1,4-bis[(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] 3-hydroxy-2-(2-methylpropyl)-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}butanedioate)