NP-MRD: Showing NP-Card for (2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate (NP0231459)

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Record Information

Version

2.0

Created at

2022-09-06 12:20:09 UTC

Updated at

2022-09-06 12:20:09 UTC

NP-MRD ID

NP0231459

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate

Description

(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-{3-hydroxy-5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate belongs to the class of organic compounds known as stilbene glycosides. Stilbene glycosides are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton. (2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate is found in Rheum rhaponticum. Based on a literature review very few articles have been published on (2S,3R,4S,5S,6R)-4,5-dihydroxy-2-{3-hydroxy-5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062214202D          

 44 47  0  0  1  0            999 V2000
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   -3.5724   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309062214202D          

 44 47  0  0  1  0            999 V2000
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   -7.1447   -9.9000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1447   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592  -10.3125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.5737   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592  -11.1375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.5737  -11.5500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447  -11.5500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.1447  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592  -16.0875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  1  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  6  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
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 40  2  0  0  0  0
 29 40  1  0  0  0  0
 14 41  2  0  0  0  0
  9 41  1  0  0  0  0
  6 42  1  0  0  0  0
 42 43  2  0  0  0  0
  3 43  1  0  0  0  0
 43 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0231459

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(\C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3OC(=O)C3=CC(OC)=C(OC)C(OC)=C3)=C2)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C31H34O13/c1-38-22-8-7-16(11-21(22)34)5-6-17-9-19(33)14-20(10-17)42-31-29(27(36)26(35)25(15-32)43-31)44-30(37)18-12-23(39-2)28(41-4)24(13-18)40-3/h5-14,25-27,29,31-36H,15H2,1-4H3/b6-5+/t25-,26-,27+,29-,31-/m1/s1

> <INCHI_KEY>
SSCYZQRUYNUJPI-MFEPHQFCSA-N

> <FORMULA>
C31H34O13

> <MOLECULAR_WEIGHT>
614.6

> <EXACT_MASS>
614.199941155

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
62.56704478571751

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-{3-hydroxy-5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate

> <JCHEM_LOGP>
2.9989375790000006

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.458249281097874

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.711278359511168

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810929914690316

> <JCHEM_POLAR_SURFACE_AREA>
182.82999999999998

> <JCHEM_REFRACTIVITY>
155.27469999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-{3-hydroxy-5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -6.668 -10.010   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -6.668 -11.550   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -5.335 -12.320   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -5.335 -13.860   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.668 -14.630   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.668 -16.170   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -8.002 -16.940   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -8.002 -18.480   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.668 -19.250   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.668 -20.790   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -5.335 -21.560   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -8.002 -21.560   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -9.336 -20.790   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0     -10.669 -21.560   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0     -12.003 -20.790   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0     -12.003 -19.250   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0     -13.337 -18.480   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -13.337 -16.940   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0     -12.003 -16.170   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0     -14.670 -19.250   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0     -16.004 -18.480   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0     -14.670 -20.790   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0     -16.004 -21.560   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0     -13.337 -21.560   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0     -13.337 -23.100   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0     -14.670 -23.870   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0     -16.004 -23.100   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0     -14.670 -25.410   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -13.337 -26.180   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -13.337 -27.720   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0     -12.003 -28.490   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0     -12.003 -30.030   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -14.670 -28.490   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0     -14.670 -30.030   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0     -13.337 -30.800   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -16.004 -27.720   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0     -17.338 -28.490   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0     -18.672 -27.720   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -16.004 -26.180   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -9.336 -19.250   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -9.336 -11.550   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   43                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   42                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   41                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   41                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   25                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   16   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   40                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31   35   37                                                  
CONECT   35   34   36                                                       
CONECT   36   35                                                            
CONECT   37   34   38   40                                                  
CONECT   38   37   39                                                       
CONECT   39   38                                                            
CONECT   40   37   29                                                       
CONECT   41   14    9                                                       
CONECT   42    6   43                                                       
CONECT   43   42    3   44                                                  
CONECT   44   43                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   94    0
END

View in JSmol

Synonyms

Value	Source
(2S,3R,4S,5S,6R)-4,5-Dihydroxy-2-{3-hydroxy-5-[(e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoic acid	Generator

Chemical Formula

C₃₁H₃₄O₁₃

Average Mass

614.6000 Da

Monoisotopic Mass

614.19994 Da

IUPAC Name

(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-{3-hydroxy-5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate

Traditional Name

(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-{3-hydroxy-5-[(E)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate

CAS Registry Number

Not Available

SMILES

COC1=CC=C(\C=C\C2=CC(O)=CC(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3OC(=O)C3=CC(OC)=C(OC)C(OC)=C3)=C2)C=C1O

InChI Identifier

InChI=1S/C31H34O13/c1-38-22-8-7-16(11-21(22)34)5-6-17-9-19(33)14-20(10-17)42-31-29(27(36)26(35)25(15-32)43-31)44-30(37)18-12-23(39-2)28(41-4)24(13-18)40-3/h5-14,25-27,29,31-36H,15H2,1-4H3/b6-5+/t25-,26-,27+,29-,31-/m1/s1

InChI Key

SSCYZQRUYNUJPI-MFEPHQFCSA-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
Rheum rhaponticum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbene glycosides. Stilbene glycosides are compounds structurally characterized by the presence of a carbohydrate moiety glycosidically linked to the stilbene skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Stilbene glycosides

Direct Parent

Stilbene glycosides

Alternative Parents

Substituents

Stilbene glycoside
Hydrolyzable tannin
Tannin
Phenolic glycoside
Hexose monosaccharide
Gallic acid or derivatives
M-methoxybenzoic acid or derivatives
O-glycosyl compound
Glycosyl compound
P-methoxybenzoic acid or derivatives
Benzoate ester
Methoxyphenol
Benzoic acid or derivatives
Anisole
Styrene
Methoxybenzene
Benzoyl
Phenoxy compound
Phenol ether
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
1-hydroxy-4-unsubstituted benzenoid
Monosaccharide
Monocyclic benzene moiety
Benzenoid
Oxane
Secondary alcohol
Carboxylic acid ester
Ether
Carboxylic acid derivative
Acetal
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Primary alcohol
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen 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	3	ChemAxon
pKa (Strongest Acidic)	8.71	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	182.83 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	155.27 m³·mol⁻¹	ChemAxon
Polarizability	62.57 Å³	ChemAxon
Number of Rings	4	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

163189468

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate (NP0231459)

MOL for NP0231459 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate)

3D MOL for NP0231459 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate)

3D SDF for NP0231459 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate)

3D-SDF for NP0231459 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate)

PDB for NP0231459 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate)

3D PDB for NP0231459 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate)

SMILES for NP0231459 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate)

INCHI for NP0231459 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate)

Structure for NP0231459 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate)

3D Structure for NP0231459 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-2-{3-hydroxy-5-[(1e)-2-(3-hydroxy-4-methoxyphenyl)ethenyl]phenoxy}-6-(hydroxymethyl)oxan-3-yl 3,4,5-trimethoxybenzoate)