NP-MRD: Showing NP-Card for (S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside (NP0029762)

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Record Information

Version

2.0

Created at

2021-06-19 21:18:03 UTC

Updated at

2021-06-29 23:57:20 UTC

NP-MRD ID

NP0029762

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside

Provided By

JEOL Database JEOL Logo

Description

(S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside is found in Alnus japonica and Alnus rubra. (S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside was first documented in 2000 (Chen, J., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192123183D          

 62 64  0  0  0  0            999 V2000
    2.4650   -0.8346   -3.0203 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2738   -0.9904   -2.7406 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7524   -2.2818   -2.1313 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7530   -2.9423   -1.1838 C   0  0  2  0  0  0  0  0  0  0  0  0
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    3.0904   -0.5515    1.4682 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1392   -0.7034    2.4701 C   0  0  0  0  0  0  0  0  0  0  0  0
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 16 17  2  0  0  0  0
  4  3  1  0  0  0  0
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M  END

     RDKit          3D

 62 64  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652306192123183D          

 62 64  0  0  0  0            999 V2000
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    1.4134   -3.9608   -0.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9553    0.6387    3.5460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3598   -1.7171    3.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1378   -3.0327    1.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6494    0.6656   -3.9172 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3087    0.7441    0.9183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8063   -0.7921    2.5648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1050   -1.3591    0.5451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8932    0.2690    1.5713 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 17  2  0  0  0  0
  4  3  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
  3  2  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 11  5  1  0  0  0  0
  8  9  1  0  0  0  0
  2 12  1  0  0  0  0
  2  1  2  0  0  0  0
  8 10  1  0  0  0  0
 19 20  1  0  0  0  0
 12 13  1  0  0  0  0
 13 23  1  0  0  0  0
  5  6  2  0  0  0  0
 13 14  1  0  0  0  0
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 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
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  5  4  1  0  0  0  0
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 24 31  1  0  0  0  0
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 24 23  1  0  0  0  0
  7 38  1  0  0  0  0
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  6 37  1  0  0  0  0
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  9 39  1  0  0  0  0
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 31 61  1  6  0  0  0
 32 62  1  0  0  0  0
 26 55  1  0  0  0  0
 26 56  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0029762

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C(=O)C([H])([H])[C@@]([H])(O[C@@]1([H])OC([H])([H])[C@]([H])(O[H])[C@@]([H])(O[H])[C@]1([H])O[H])C([H])([H])C([H])([H])C1=C([H])C([H])=C(O[H])C([H])=C1[H]

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O8/c25-17-7-1-15(2-8-17)5-11-19(27)13-20(12-6-16-3-9-18(26)10-4-16)32-24-23(30)22(29)21(28)14-31-24/h1-4,7-10,20-26,28-30H,5-6,11-14H2/t20-,21-,22+,23-,24+/m0/s1

> <INCHI_KEY>
GTGWRSYHHGXYAS-OSFFKXSWSA-N

> <FORMULA>
C24H30O8

> <MOLECULAR_WEIGHT>
446.496

> <EXACT_MASS>
446.194067926

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
45.29003389210759

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5S)-1,7-bis(4-hydroxyphenyl)-5-{[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}heptan-3-one

> <ALOGPS_LOGP>
1.71

> <JCHEM_LOGP>
2.5747916936666675

> <ALOGPS_LOGS>
-3.46

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.356177794323388

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.439438361976281

> <JCHEM_PKA_STRONGEST_BASIC>
-3.526580621612222

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
115.97070000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.54e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5S)-1,7-bis(4-hydroxyphenyl)-5-{[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}heptan-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

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 13 44  1  6
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 26 55  1  0
 26 56  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  O   UNK     0       2.465  -0.835  -3.020  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.274  -0.990  -2.741  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.752  -2.282  -2.131  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.753  -2.942  -1.184  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.909  -2.191   0.117  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.977  -1.300   0.296  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.090  -0.552   1.468  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.139  -0.703   2.470  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.199   0.030   3.618  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.089  -1.601   2.325  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.970  -2.342   1.148  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.262   0.092  -3.067  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.022   1.028  -1.889  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.251   1.710  -1.363  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.943   2.756  -0.282  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.147   3.144   0.547  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.365   3.506  -0.048  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.466   3.855   0.738  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.347   3.857   2.123  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.398   4.184   2.927  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.146   3.524   2.733  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.048   3.171   1.947  0.00  0.00           C+0
HETATM   23  O   UNK     0      -0.605   0.290  -0.811  0.00  0.00           O+0
HETATM   24  C   UNK     0      -2.027   0.416  -0.720  0.00  0.00           C+0
HETATM   25  O   UNK     0      -2.659  -0.165  -1.858  0.00  0.00           O+0
HETATM   26  C   UNK     0      -4.084  -0.073  -1.786  0.00  0.00           C+0
HETATM   27  C   UNK     0      -4.633  -0.808  -0.564  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.047  -0.635  -0.472  0.00  0.00           O+0
HETATM   29  C   UNK     0      -3.966  -0.276   0.705  0.00  0.00           C+0
HETATM   30  O   UNK     0      -4.388  -1.068   1.827  0.00  0.00           O+0
HETATM   31  C   UNK     0      -2.448  -0.317   0.567  0.00  0.00           C+0
HETATM   32  O   UNK     0      -1.860   0.282   1.732  0.00  0.00           O+0
HETATM   33  H   UNK     0       0.538  -2.957  -2.968  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.195  -2.094  -1.616  0.00  0.00           H+0
HETATM   35  H   UNK     0       2.731  -3.057  -1.667  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.413  -3.961  -0.956  0.00  0.00           H+0
HETATM   37  H   UNK     0       3.712  -1.162  -0.496  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.912   0.151   1.571  0.00  0.00           H+0
HETATM   39  H   UNK     0       2.955   0.639   3.546  0.00  0.00           H+0
HETATM   40  H   UNK     0       0.360  -1.717   3.122  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.138  -3.033   1.037  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.649   0.666  -3.917  0.00  0.00           H+0
HETATM   43  H   UNK     0      -0.650  -0.403  -3.415  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.710   1.812  -2.231  0.00  0.00           H+0
HETATM   45  H   UNK     0       1.918   0.956  -0.935  0.00  0.00           H+0
HETATM   46  H   UNK     0       1.787   2.184  -2.194  0.00  0.00           H+0
HETATM   47  H   UNK     0       0.532   3.660  -0.747  0.00  0.00           H+0
HETATM   48  H   UNK     0       0.166   2.373   0.390  0.00  0.00           H+0
HETATM   49  H   UNK     0       3.469   3.513  -1.131  0.00  0.00           H+0
HETATM   50  H   UNK     0       5.400   4.121   0.252  0.00  0.00           H+0
HETATM   51  H   UNK     0       6.150   4.437   2.366  0.00  0.00           H+0
HETATM   52  H   UNK     0       3.060   3.544   3.816  0.00  0.00           H+0
HETATM   53  H   UNK     0       1.113   2.908   2.439  0.00  0.00           H+0
HETATM   54  H   UNK     0      -2.275   1.484  -0.645  0.00  0.00           H+0
HETATM   55  H   UNK     0      -4.386   0.982  -1.787  0.00  0.00           H+0
HETATM   56  H   UNK     0      -4.499  -0.511  -2.700  0.00  0.00           H+0
HETATM   57  H   UNK     0      -4.439  -1.884  -0.657  0.00  0.00           H+0
HETATM   58  H   UNK     0      -6.293  -0.997   0.404  0.00  0.00           H+0
HETATM   59  H   UNK     0      -4.309   0.744   0.918  0.00  0.00           H+0
HETATM   60  H   UNK     0      -3.806  -0.792   2.565  0.00  0.00           H+0
HETATM   61  H   UNK     0      -2.105  -1.359   0.545  0.00  0.00           H+0
HETATM   62  H   UNK     0      -0.893   0.269   1.571  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    3   12    1                                                  
CONECT    3    4    2   33   34                                             
CONECT    4    3    5   35   36                                             
CONECT    5   11    6    4                                                  
CONECT    6    5    7   37                                                  
CONECT    7    6    8   38                                                  
CONECT    8    9   10    7                                                  
CONECT    9    8   39                                                       
CONECT   10    8   11   40                                                  
CONECT   11    5   10   41                                                  
CONECT   12    2   13   42   43                                             
CONECT   13   12   23   14   44                                             
CONECT   14   13   15   45   46                                             
CONECT   15   14   16   47   48                                             
CONECT   16   17   15   22                                                  
CONECT   17   16   18   49                                                  
CONECT   18   17   19   50                                                  
CONECT   19   18   21   20                                                  
CONECT   20   19   51                                                       
CONECT   21   19   22   52                                                  
CONECT   22   21   16   53                                                  
CONECT   23   13   24                                                       
CONECT   24   31   25   23   54                                             
CONECT   25   26   24                                                       
CONECT   26   27   25   55   56                                             
CONECT   27   29   26   28   57                                             
CONECT   28   27   58                                                       
CONECT   29   31   27   30   59                                             
CONECT   30   29   60                                                       
CONECT   31   24   29   32   61                                             
CONECT   32   31   62                                                       
CONECT   33    3                                                            
CONECT   34    3                                                            
CONECT   35    4                                                            
CONECT   36    4                                                            
CONECT   37    6                                                            
CONECT   38    7                                                            
CONECT   39    9                                                            
CONECT   40   10                                                            
CONECT   41   11                                                            
CONECT   42   12                                                            
CONECT   43   12                                                            
CONECT   44   13                                                            
CONECT   45   14                                                            
CONECT   46   14                                                            
CONECT   47   15                                                            
CONECT   48   15                                                            
CONECT   49   17                                                            
CONECT   50   18                                                            
CONECT   51   20                                                            
CONECT   52   21                                                            
CONECT   53   22                                                            
CONECT   54   24                                                            
CONECT   55   26                                                            
CONECT   56   26                                                            
CONECT   57   27                                                            
CONECT   58   28                                                            
CONECT   59   29                                                            
CONECT   60   30                                                            
CONECT   61   31                                                            
CONECT   62   32                                                            
MASTER        0    0    0    0    0    0    0    0   62    0  128    0
END

RDKit          3D

62 64  0  0  0  0  0  0  0  0999 V2000
    2.4650   -0.8346   -3.0203 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2738   -0.9904   -2.7406 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7524   -2.2818   -2.1313 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7530   -2.9423   -1.1838 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9085   -2.1905    0.1172 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9765   -1.3002    0.2955 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0904   -0.5515    1.4682 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1392   -0.7034    2.4701 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1992    0.0302    3.6179 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0892   -1.6013    2.3250 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9701   -2.3420    1.1477 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2623    0.0916   -3.0668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0215    1.0278   -1.8890 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2513    1.7096   -1.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9433    2.7564   -0.2815 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1475    3.1439    0.5474 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3646    3.5057   -0.0480 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4664    3.8553    0.7377 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3472    3.8574    2.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3979    4.1845    2.9271 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1457    3.5241    2.7327 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0476    3.1705    1.9473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6047    0.2900   -0.8114 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0267    0.4164   -0.7204 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6585   -0.1647   -1.8580 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0836   -0.0730   -1.7856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6332   -0.8081   -0.5640 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.0469   -0.6346   -0.4715 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9664   -0.2763    0.7049 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3875   -1.0684    1.8266 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4476   -0.3171    0.5665 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8603    0.2815    1.7319 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5381   -2.9568   -2.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1945   -2.0940   -1.6164 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7314   -3.0570   -1.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4134   -3.9608   -0.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7120   -1.1619   -0.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9118    0.1511    1.5709 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9553    0.6387    3.5460 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3598   -1.7171    3.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1378   -3.0327    1.0374 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6494    0.6656   -3.9172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6500   -0.4032   -3.4153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7099    1.8122   -2.2305 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9177    0.9559   -0.9353 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7867    2.1844   -2.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5316    3.6604   -0.7470 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1659    2.3732    0.3899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4690    3.5134   -1.1305 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3999    4.1208    0.2517 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1496    4.4369    2.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0600    3.5441    3.8155 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1130    2.9075    2.4394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2750    1.4836   -0.6448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3862    0.9817   -1.7868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4986   -0.5115   -2.6997 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4395   -1.8837   -0.6568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2926   -0.9969    0.4040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3087    0.7441    0.9183 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8063   -0.7921    2.5648 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1050   -1.3591    0.5451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8932    0.2690    1.5713 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 17  2  0
  4  3  1  0
 17 18  1  0
 18 19  2  0
  3  2  1  0
 19 21  1  0
 21 22  2  0
 11  5  1  0
  8  9  1  0
  2 12  1  0
  2  1  2  0
  8 10  1  0
 19 20  1  0
 12 13  1  0
 13 23  1  0
  5  6  2  0
 13 14  1  0
  6  7  1  0
 14 15  1  0
 15 16  1  0
  7  8  2  0
  5  4  1  0
 22 16  1  0
 10 11  2  0
 24 31  1  0
 31 29  1  0
 29 27  1  0
 27 26  1  0
 26 25  1  0
 25 24  1  0
 27 28  1  0
 29 30  1  0
 31 32  1  0
 24 23  1  0
  7 38  1  0
 10 40  1  0
 11 41  1  0
  6 37  1  0
  4 35  1  0
  4 36  1  0
  3 33  1  0
  3 34  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  6
 14 45  1  0
 14 46  1  0
 15 47  1  0
 15 48  1  0
 22 53  1  0
 17 49  1  0
 18 50  1  0
 21 52  1  0
  9 39  1  0
 20 51  1  0
 24 54  1  1
 27 57  1  6
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 29 59  1  1
 30 60  1  0
 31 61  1  6
 32 62  1  0
 26 55  1  0
 26 56  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₀O₈

Average Mass

446.4960 Da

Monoisotopic Mass

446.19407 Da

IUPAC Name

(5S)-1,7-bis(4-hydroxyphenyl)-5-{[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}heptan-3-one

Traditional Name

(5S)-1,7-bis(4-hydroxyphenyl)-5-{[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}heptan-3-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C(=O)C([H])([H])[C@@]([H])(O[C@@]1([H])OC([H])([H])[C@]([H])(O[H])[C@@]([H])(O[H])[C@]1([H])O[H])C([H])([H])C([H])([H])C1=C([H])C([H])=C(O[H])C([H])=C1[H]

InChI Identifier

InChI=1S/C24H30O8/c25-17-7-1-15(2-8-17)5-11-19(27)13-20(12-6-16-3-9-18(26)10-4-16)32-24-23(30)22(29)21(28)14-31-24/h1-4,7-10,20-26,28-30H,5-6,11-14H2/t20-,21-,22+,23-,24+/m0/s1

InChI Key

GTGWRSYHHGXYAS-OSFFKXSWSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CD₃OD, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Alnus japonica	Plant	KNApSAcK
Alnus rubra	JEOL database	Chen, J., et al, Phytochemistry 53, 971 (2000)

Chemical Taxonomy

Classification

Not classified

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	1.71	ALOGPS
logP	2.57	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	9.44	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	115.97 m³·mol⁻¹	ChemAxon
Polarizability	45.29 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

Not Available

References

General References

Chen, J., et al. (2000). Chen, J., et al, Phytochemistry 53, 971 (2000). Phytochem..

Showing NP-Card for (S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside (NP0029762)

MOL for NP0029762 ((S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside)

3D MOL for NP0029762 ((S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside)

3D SDF for NP0029762 ((S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside)

3D-SDF for NP0029762 ((S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside)

PDB for NP0029762 ((S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside)

3D PDB for NP0029762 ((S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside)

SMILES for NP0029762 ((S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside)

INCHI for NP0029762 ((S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside)

Structure for NP0029762 ((S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside)

3D Structure for NP0029762 ((S)-1,7-bis-(4-hydroxyphenyl)-heptan-3-one-5-O-beta-D-xylopyranoside)