NP-MRD: Showing NP-Card for {3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate (NP0242036)

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Record Information

Version

1.0

Created at

2022-09-07 02:15:02 UTC

Updated at

2022-09-07 02:15:02 UTC

NP-MRD ID

NP0242036

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

{3,4,5-Trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate 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. {3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate is found in Lilium henryi and Lilium mackliniae. {3,4,5-Trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171516312D          

 60 64  0  0  0  0            999 V2000
   -6.8870   -5.4162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.1462   -6.7331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9747   -7.5400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1901   -7.7950    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5770   -7.2429    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7923   -7.4979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6208   -8.3049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1793   -6.9458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3946   -7.2008    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1397   -7.9854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6246   -8.6528    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3147   -7.9854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2225   -6.7677    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.6824   -8.2225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6973   -3.8581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.5439   -7.0302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3286   -6.7752    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
 29 27  1  4  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
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 34 47  1  0  0  0  0
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 22 55  1  0  0  0  0
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 57 58  1  0  0  0  0
 58 59  2  0  0  0  0
  3 59  1  0  0  0  0
 59 60  1  0  0  0  0
M  END

     RDKit          3D

108112  0  0  0  0  0  0  0  0999 V2000
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   -8.9379    2.1034   -1.8403 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0084    3.1860   -1.6580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9607    3.3841   -0.9530 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.5201   -0.0731    2.1759 C   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>
NP0242036

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(C=CC(=O)OC2C(O)C(CO)OC2(CO)OC2OC(COC(=O)C=CC3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(OC)=C3)C(O)C(O)C2O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C38H48O22/c1-52-21-11-17(3-7-19(21)42)6-10-27(44)58-35-30(47)24(14-40)59-38(35,16-41)60-37-34(51)32(49)29(46)25(57-37)15-54-26(43)9-5-18-4-8-20(22(12-18)53-2)55-36-33(50)31(48)28(45)23(13-39)56-36/h3-12,23-25,28-37,39-42,45-51H,13-16H2,1-2H3

> <INCHI_KEY>
LNADBRJCSVTTPA-UHFFFAOYSA-N

> <FORMULA>
C38H48O22

> <MOLECULAR_WEIGHT>
856.78

> <EXACT_MASS>
856.263723186

> <JCHEM_ACCEPTOR_COUNT>
20

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
83.87266186138055

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
11

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-0.23

> <JCHEM_LOGP>
-1.6515947956666652

> <ALOGPS_LOGS>
-2.92

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.868331504539821

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.863368737340101

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6483953658794537

> <JCHEM_POLAR_SURFACE_AREA>
339.74

> <JCHEM_REFRACTIVITY>
196.9421

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.03e+00 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0     -12.856 -10.110   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -11.391 -10.586   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0     -11.071 -12.092   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.606 -12.568   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -9.286 -14.075   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.821 -14.551   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.677 -13.520   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.212 -13.996   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -4.892 -15.502   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -4.068 -12.966   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.603 -13.441   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.127 -14.906   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -3.033 -16.152   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -0.587 -14.906   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.318 -16.152   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       1.849 -15.991   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      -0.112 -13.441   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.357 -12.536   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.601 -11.195   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.938 -11.178   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -2.113 -11.195   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.329  -9.869   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.210  -9.885   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.994  -8.560   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.534  -8.576   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.290  -9.917   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.830  -9.934   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.614  -8.608   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.586 -11.275   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.126 -11.291   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.882 -12.633   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.422 -12.649   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.178 -13.991   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.394 -15.316   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      10.150 -16.658   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      11.690 -16.674   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      12.474 -15.349   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      14.014 -15.365   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      14.798 -14.039   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      16.338 -14.055   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      14.770 -16.706   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      16.310 -16.723   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      13.986 -18.032   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      14.742 -19.374   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      12.446 -18.016   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      11.662 -19.341   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       7.854 -15.300   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       7.070 -16.626   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       5.530 -16.610   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       7.098 -13.959   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       0.238  -7.218   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       1.022  -5.892   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      -1.302  -7.202   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      -2.058  -5.860   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      -2.085  -8.527   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0      -3.625  -8.511   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0     -10.431 -15.105   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0     -11.895 -14.629   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0     -12.215 -13.123   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0     -13.680 -12.647   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   59                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   57                                                  
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   55                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   51                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   50                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   47                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   45                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   41                                                  
CONECT   39   38   40                                                       
CONECT   40   39                                                            
CONECT   41   38   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   36   46                                                  
CONECT   46   45                                                            
CONECT   47   34   48   50                                                  
CONECT   48   47   49                                                       
CONECT   49   48                                                            
CONECT   50   47   31                                                       
CONECT   51   24   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51   54   55                                                  
CONECT   54   53                                                            
CONECT   55   53   22   56                                                  
CONECT   56   55                                                            
CONECT   57    5   58                                                       
CONECT   58   57   59                                                       
CONECT   59   58    3   60                                                  
CONECT   60   59                                                            
MASTER        0    0    0    0    0    0    0    0   60    0  128    0
END

View in JSmol

Synonyms

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

Chemical Formula

C₃₈H₄₈O₂₂

Average Mass

856.7800 Da

Monoisotopic Mass

856.26372 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

COC1=CC(C=CC(=O)OC2C(O)C(CO)OC2(CO)OC2OC(COC(=O)C=CC3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(OC)=C3)C(O)C(O)C2O)=CC=C1O

InChI Identifier

InChI=1S/C38H48O22/c1-52-21-11-17(3-7-19(21)42)6-10-27(44)58-35-30(47)24(14-40)59-38(35,16-41)60-37-34(51)32(49)29(46)25(57-37)15-54-26(43)9-5-18-4-8-20(22(12-18)53-2)55-36-33(50)31(48)28(45)23(13-39)56-36/h3-12,23-25,28-37,39-42,45-51H,13-16H2,1-2H3

InChI Key

LNADBRJCSVTTPA-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
Lilium henryi	LOTUS Database	35616633
Lilium mackliniae	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 or derivatives
Coumaric acid or derivatives
Hydroxycinnamic acid or derivatives
Cinnamic acid ester
C-glycosyl compound
Disaccharide
O-glycosyl compound
Methoxyphenol
Anisole
Phenoxy compound
Methoxybenzene
Phenol ether
Styrene
1-hydroxy-2-unsubstituted benzenoid
Ketal
Fatty acid ester
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Oxane
Dicarboxylic acid or derivatives
Fatty acyl
Benzenoid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Acetal
Oxacycle
Carboxylic acid derivative
Ether
Polyol
Organoheterocyclic compound
Primary alcohol
Alcohol
Carbonyl group
Organic oxide
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	-0.23	ALOGPS
logP	-1.7	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	9.86	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	20	ChemAxon
Hydrogen Donor Count	11	ChemAxon
Polar Surface Area	339.74 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	196.94 m³·mol⁻¹	ChemAxon
Polarizability	83.87 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 {3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate (NP0242036)

MOL for NP0242036 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate)

3D MOL for NP0242036 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate)

3D SDF for NP0242036 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate)

3D-SDF for NP0242036 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate)

PDB for NP0242036 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate)

3D PDB for NP0242036 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate)

SMILES for NP0242036 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate)

INCHI for NP0242036 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate)

Structure for NP0242036 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate)

3D Structure for NP0242036 ({3,4,5-trihydroxy-6-[(4-hydroxy-3-{[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}-2,5-bis(hydroxymethyl)oxolan-2-yl)oxy]oxan-2-yl}methyl 3-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoate)