NP-MRD: Showing NP-Card for 3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one (NP0217497)

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Record Information

Version

2.0

Created at

2022-09-05 17:51:58 UTC

Updated at

2022-09-05 17:51:58 UTC

NP-MRD ID

NP0217497

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one

Description

3-Hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones. 3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one is found in Trachelospermum asiaticum. 3-Hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261504182D          

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M  END

     RDKit          3D

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M  END


  Mrv1533004261504182D          

 49 53  0  0  0  0            999 V2000
    9.7552   -2.7985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1421   -2.2465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3575   -2.5014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7444   -1.9494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9597   -2.2043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3467   -1.6523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5620   -1.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3071   -2.6919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4821   -2.6919    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2272   -1.9072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4425   -1.6523    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8946   -1.4223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4896   -0.7036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2996   -0.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8796    0.0065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0547   -0.0021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6347    0.7080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0397    1.4268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6197    2.1369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0247    2.8556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8497    2.8643    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2547    3.5830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0797    3.5917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4846    4.3104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8347    4.2931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2397    5.0119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0098    4.2845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5898    4.9946    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6048    3.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7798    3.5571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8647    1.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2697    2.1542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0946    2.1628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2846    0.7253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7882   -3.0113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4013   -3.5633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1859   -3.3084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7990   -3.8604    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6275   -4.6674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2406   -5.2194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0691   -6.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6822   -6.5784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5106   -7.3854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2844   -6.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1129   -7.0883    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6714   -5.7293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8867   -5.9843    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8429   -4.9223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2298   -4.3703    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
  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  2  0  0  0  0
 10 12  1  0  0  0  0
  7 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  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 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
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 20 29  1  0  0  0  0
 29 30  1  0  0  0  0
 18 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  2  0  0  0  0
 15 34  1  0  0  0  0
  5 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
  3 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 41 44  1  0  0  0  0
 44 45  1  0  0  0  0
 44 46  1  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 39 48  1  0  0  0  0
 48 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0217497

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(CC2COC(=O)C2(O)CC2=CC=C(OC3OC(CO)C(O)C(O)C3O)C(OC)=C2)=CC=C1OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C32H42O17/c1-43-19-8-14(3-5-17(19)46-29-27(39)25(37)23(35)21(11-33)48-29)7-16-13-45-31(41)32(16,42)10-15-4-6-18(20(9-15)44-2)47-30-28(40)26(38)24(36)22(12-34)49-30/h3-6,8-9,16,21-30,33-40,42H,7,10-13H2,1-2H3

> <INCHI_KEY>
DXVTWMJZLMHILX-UHFFFAOYSA-N

> <FORMULA>
C32H42O17

> <MOLECULAR_WEIGHT>
698.671

> <EXACT_MASS>
698.242199892

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
68.94522120884477

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-0.68

> <JCHEM_LOGP>
-2.1061295316666646

> <ALOGPS_LOGS>
-2.93

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.113687478064985

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.64428414735677

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092354907191

> <JCHEM_POLAR_SURFACE_AREA>
263.74999999999994

> <JCHEM_REFRACTIVITY>
161.37840000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.27e-01 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      18.210  -5.224   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      17.065  -4.193   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      15.601  -4.669   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      14.456  -3.639   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.992  -4.115   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.847  -3.084   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      10.382  -3.560   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.907  -5.025   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       8.367  -5.025   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.891  -3.560   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.426  -3.084   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.137  -2.655   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.381  -1.313   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.893  -1.313   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.109   0.012   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.569  -0.004   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.785   1.322   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.541   2.663   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.757   3.989   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.513   5.331   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.053   5.347   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       9.809   6.688   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.349   6.704   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.105   8.046   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.025   8.014   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.781   9.356   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       7.485   7.998   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.701   9.323   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.729   6.656   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       5.189   6.640   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       9.081   2.679   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.837   4.021   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      11.377   4.037   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.865   1.354   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.671  -5.621   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.816  -6.652   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      15.280  -6.176   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      16.425  -7.206   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      16.105  -8.712   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      17.249  -9.743   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      16.929 -11.249   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      18.073 -12.280   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      17.753 -13.786   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      15.464 -11.725   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      15.144 -13.232   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      14.320 -10.695   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      12.855 -11.171   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      14.640  -9.188   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      13.496  -8.158   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   37                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   35                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    7   13   14                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   34                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   31                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   29                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   20   30                                                  
CONECT   30   29                                                            
CONECT   31   18   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31   15                                                       
CONECT   35    5   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36    3   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   48                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   44                                                  
CONECT   42   41   43                                                       
CONECT   43   42                                                            
CONECT   44   41   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   39   49                                                  
CONECT   49   48                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₄₂O₁₇

Average Mass

698.6710 Da

Monoisotopic Mass

698.24220 Da

IUPAC Name

3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one

Traditional Name

3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one

CAS Registry Number

Not Available

SMILES

COC1=CC(CC2COC(=O)C2(O)CC2=CC=C(OC3OC(CO)C(O)C(O)C3O)C(OC)=C2)=CC=C1OC1OC(CO)C(O)C(O)C1O

InChI Identifier

InChI=1S/C32H42O17/c1-43-19-8-14(3-5-17(19)46-29-27(39)25(37)23(35)21(11-33)48-29)7-16-13-45-31(41)32(16,42)10-15-4-6-18(20(9-15)44-2)47-30-28(40)26(38)24(36)22(12-34)49-30/h3-6,8-9,16,21-30,33-40,42H,7,10-13H2,1-2H3

InChI Key

DXVTWMJZLMHILX-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
Trachelospermum asiaticum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Lignan glycosides

Sub Class

Not Available

Direct Parent

Lignan glycosides

Alternative Parents

Substituents

Lignan glycoside
Dibenzylbutyrolactone
Lignan lactone
Tetrahydrofuran lignan
9,9p-epoxylignan
Furanoid lignan
Phenolic glycoside
Fatty acyl glycoside of mono- or disaccharide
Fatty acyl glycoside
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
Methoxybenzene
Phenol ether
Anisole
Phenoxy compound
Alkyl aryl ether
Oxane
Fatty acyl
Benzenoid
Monosaccharide
Gamma butyrolactone
Monocyclic benzene moiety
Tertiary alcohol
Tetrahydrofuran
Secondary alcohol
Carboxylic acid ester
Lactone
Monocarboxylic acid or derivatives
Polyol
Ether
Organoheterocyclic compound
Carboxylic acid derivative
Oxacycle
Acetal
Organooxygen compound
Primary alcohol
Carbonyl group
Organic oxide
Alcohol
Hydrocarbon derivative
Organic oxygen compound
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	-0.68	ALOGPS
logP	-2.1	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	11.64	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	263.75 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	161.38 m³·mol⁻¹	ChemAxon
Polarizability	68.95 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one (NP0217497)

MOL for NP0217497 (3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one)

3D MOL for NP0217497 (3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one)

3D SDF for NP0217497 (3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one)

3D-SDF for NP0217497 (3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one)

PDB for NP0217497 (3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one)

3D PDB for NP0217497 (3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one)

SMILES for NP0217497 (3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one)

INCHI for NP0217497 (3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one)

Structure for NP0217497 (3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one)

3D Structure for NP0217497 (3-hydroxy-3,4-bis[(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]oxolan-2-one)