NP-MRD: Showing NP-Card for 1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate (NP0190773)

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Record Information

Version

2.0

Created at

2022-09-04 07:30:42 UTC

Updated at

2022-09-04 07:30:43 UTC

NP-MRD ID

NP0190773

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

(S)-2-Hydroxy-2-isopropylbutanedioic acid bis[4-(beta-D-glucopyranosyloxy)benzyl] ester 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-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate is found in Galeola faberi. Based on a literature review very few articles have been published on (S)-2-Hydroxy-2-isopropylbutanedioic acid bis[4-(beta-D-glucopyranosyloxy)benzyl] ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042209302D          

 50 53  0  0  1  0            999 V2000
    8.1612   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4467   -4.8099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4467   -5.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7322   -4.3974    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3197   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0177   -3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3033   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888   -3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
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 47 48  1  1  0  0  0
 36 49  1  0  0  0  0
 49 50  2  0  0  0  0
 33 50  1  0  0  0  0
M  END

     RDKit          3D

 94 97  0  0  0  0  0  0  0  0999 V2000
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 28 77  1  0
 32 78  1  0
 32 79  1  0
 34 80  1  0
 35 81  1  0
 38 82  1  1
 40 83  1  1
 41 84  1  0
 41 85  1  0
 42 86  1  0
 43 87  1  6
 44 88  1  0
 45 89  1  1
 46 90  1  0
 47 91  1  6
 48 92  1  0
 49 93  1  0
 50 94  1  0
M  END


  Mrv1652309042209302D          

 50 53  0  0  1  0            999 V2000
    8.1612   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4467   -4.8099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4467   -5.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7322   -4.3974    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3197   -5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0177   -3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3033   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888   -3.9849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3033   -5.2224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888   -5.6349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888   -6.4599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3033   -6.8724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3033   -7.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888   -8.1099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888   -8.9349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8743   -9.3474    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8743  -10.1724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599  -10.5849    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1599  -11.4099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454  -11.8224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454  -10.1724    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7309  -10.5849    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4454   -9.3474    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7309   -8.9349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1599   -8.9349    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1599   -8.1099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8743   -7.6974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8743   -6.8724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9697   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7322   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9072   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4947   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6697   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2572   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6697   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2572   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6697    0.6039    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2572    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6697    2.0329    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2572    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4322    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4947    2.0329    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9072    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9072    1.3184    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.7322    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4947    0.6039    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9072   -0.1105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4947   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9072   -1.5395    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  6  0  0  0
  4  6  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  1  1  0  0  0
 14 27  1  0  0  0  0
 27 28  2  0  0  0  0
 11 28  1  0  0  0  0
  4 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  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  2  0  0  0  0
 36 37  1  0  0  0  0
 38 37  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  6  0  0  0
 41 42  1  0  0  0  0
 40 43  1  0  0  0  0
 43 44  1  1  0  0  0
 43 45  1  0  0  0  0
 45 46  1  6  0  0  0
 45 47  1  0  0  0  0
 38 47  1  0  0  0  0
 47 48  1  1  0  0  0
 36 49  1  0  0  0  0
 49 50  2  0  0  0  0
 33 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0190773

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@](O)(CC(=O)OCC1=CC=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1)C(=O)OCC1=CC=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C33H44O17/c1-16(2)33(44,32(43)46-15-18-5-9-20(10-6-18)48-31-29(42)27(40)25(38)22(13-35)50-31)11-23(36)45-14-17-3-7-19(8-4-17)47-30-28(41)26(39)24(37)21(12-34)49-30/h3-10,16,21-22,24-31,34-35,37-42,44H,11-15H2,1-2H3/t21-,22-,24-,25-,26+,27+,28-,29-,30-,31-,33+/m1/s1

> <INCHI_KEY>
DTPHGPMYQBNIDH-HWUIEBOVSA-N

> <FORMULA>
C33H44O17

> <MOLECULAR_WEIGHT>
712.698

> <EXACT_MASS>
712.257849957

> <JCHEM_ACCEPTOR_COUNT>
15

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
71.31846028141356

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <JCHEM_LOGP>
-1.1959128040000007

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.092833202998564

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.609233918937353

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092343686494

> <JCHEM_POLAR_SURFACE_AREA>
271.59

> <JCHEM_REFRACTIVITY>
165.5981

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      15.234  -8.208   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.900  -8.978   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.900 -10.518   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.567  -8.208   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      11.797  -9.542   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      11.233  -7.438   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.899  -8.208   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       8.566  -7.438   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       9.899  -9.748   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       8.566 -10.518   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.566 -12.058   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.899 -12.828   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.899 -14.368   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.566 -15.138   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       8.566 -16.678   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.232 -17.448   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.232 -18.988   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.898 -19.758   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.898 -21.298   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.565 -22.068   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.565 -18.988   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.231 -19.758   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       4.565 -17.448   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.231 -16.678   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.898 -16.678   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.898 -15.138   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       7.232 -14.368   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.232 -12.828   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.337  -6.875   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      14.877  -6.875   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      12.567  -5.541   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      11.027  -5.541   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.257  -4.207   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       8.717  -4.207   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.947  -2.874   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.717  -1.540   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       7.947  -0.206   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       8.717   1.127   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       7.947   2.461   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       8.717   3.795   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.947   5.128   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       6.407   5.128   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      10.257   3.795   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      11.027   5.128   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      11.027   2.461   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      12.567   2.461   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      10.257   1.127   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      11.027  -0.206   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      10.257  -1.540   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      11.027  -2.874   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6   29                                             
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   28                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   27                                                  
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                                                            
CONECT   27   14   28                                                       
CONECT   28   27   11                                                       
CONECT   29    4   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   50                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37   49                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39   47                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   43                                                  
CONECT   41   40   42                                                       
CONECT   42   41                                                            
CONECT   43   40   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   38   48                                                  
CONECT   48   47                                                            
CONECT   49   36   50                                                       
CONECT   50   49   33                                                       
MASTER        0    0    0    0    0    0    0    0   50    0  106    0
END

View in JSmol

Synonyms

Value	Source
(S)-2-Hydroxy-2-isopropylbutanedioate bis[4-(b-D-glucopyranosyloxy)benzyl] ester	Generator
(S)-2-Hydroxy-2-isopropylbutanedioate bis[4-(beta-D-glucopyranosyloxy)benzyl] ester	Generator
(S)-2-Hydroxy-2-isopropylbutanedioate bis[4-(β-D-glucopyranosyloxy)benzyl] ester	Generator
(S)-2-Hydroxy-2-isopropylbutanedioic acid bis[4-(b-D-glucopyranosyloxy)benzyl] ester	Generator
(S)-2-Hydroxy-2-isopropylbutanedioic acid bis[4-(β-D-glucopyranosyloxy)benzyl] ester	Generator

Chemical Formula

C₃₃H₄₄O₁₇

Average Mass

712.6980 Da

Monoisotopic Mass

712.25785 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

CC(C)[C@@](O)(CC(=O)OCC1=CC=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1)C(=O)OCC1=CC=C(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)C=C1

InChI Identifier

InChI=1S/C33H44O17/c1-16(2)33(44,32(43)46-15-18-5-9-20(10-6-18)48-31-29(42)27(40)25(38)22(13-35)50-31)11-23(36)45-14-17-3-7-19(8-4-17)47-30-28(41)26(39)24(37)21(12-34)49-30/h3-10,16,21-22,24-31,34-35,37-42,44H,11-15H2,1-2H3/t21-,22-,24-,25-,26+,27+,28-,29-,30-,31-,33+/m1/s1

InChI Key

DTPHGPMYQBNIDH-HWUIEBOVSA-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
Galeola faberi	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
Hexose monosaccharide
O-glycosyl compound
Benzyloxycarbonyl
Phenoxy compound
Phenol ether
Fatty acid ester
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Monosaccharide
Fatty acyl
Oxane
Benzenoid
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Acetal
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Polyol
Organic oxide
Hydrocarbon derivative
Alcohol
Primary alcohol
Carbonyl group
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	-1.2	ChemAxon
pKa (Strongest Acidic)	11.61	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	15	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	271.59 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	165.6 m³·mol⁻¹	ChemAxon
Polarizability	71.32 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

53778574

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-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate (NP0190773)

MOL for NP0190773 (1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate)

3D MOL for NP0190773 (1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate)

3D SDF for NP0190773 (1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate)

3D-SDF for NP0190773 (1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate)

PDB for NP0190773 (1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate)

3D PDB for NP0190773 (1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate)

SMILES for NP0190773 (1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate)

INCHI for NP0190773 (1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate)

Structure for NP0190773 (1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate)

3D Structure for NP0190773 (1,4-bis[(4-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl] (2s)-2-hydroxy-2-isopropylbutanedioate)