NP-MRD: Showing NP-Card for Askendoside G (NP0073377)

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Record Information

Version

2.0

Created at

2022-04-28 18:38:21 UTC

Updated at

2022-04-28 18:38:21 UTC

NP-MRD ID

NP0073377

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Askendoside G

Description

(2R,3R,4S,5S,6R)-2-{[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-6-{[(2S,3R,4S,5R)-4,5-dihydroxy-3-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]oxy}-15-[(2R,5R)-5,6-dihydroxy-6-methylheptan-2-yl]-9-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-14-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus. Askendoside G is found in Astragalus campylosema Boiss. ssp. campylosema and Astragalus pendulus. Based on a literature review very few articles have been published on (2R,3R,4S,5S,6R)-2-{[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-6-{[(2S,3R,4S,5R)-4,5-dihydroxy-3-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]oxy}-15-[(2R,5R)-5,6-dihydroxy-6-methylheptan-2-yl]-9-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecan-14-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282220382D          

 64 71  0  0  1  0            999 V2000
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   -0.8121   -0.9702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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    0.5318   -1.4557    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8121   -0.6798    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2803   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -0.5346    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1561   -1.1653    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8758   -1.9412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0636   -2.0864    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7833   -2.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2485   -0.2441    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7167    0.3866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9045    0.2414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6083    0.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0730   -0.2709    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3024   -1.0634    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6195   -1.5264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0783   -1.3437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.9994   -2.4362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1446   -3.2483    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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   -0.8921   -2.1544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6242   -1.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9045   -1.8914    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3727   -2.5221    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6530   -3.2980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.8758    0.2912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.1273    1.6978    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7454   -4.2191    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  1  0  0  0  0
  4  5  1  1  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  1  6  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  7 15  1  0  0  0  0
 13 16  1  1  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 12 19  1  0  0  0  0
 18 20  1  1  0  0  0
 21 20  1  6  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
 21 26  1  0  0  0  0
 26 27  1  1  0  0  0
 25 28  1  6  0  0  0
 24 29  1  1  0  0  0
 23 30  1  6  0  0  0
 30 31  1  0  0  0  0
 17 32  1  1  0  0  0
 32 33  1  0  0  0  0
 33 34  1  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
 36 38  1  0  0  0  0
 36 39  1  0  0  0  0
 35 40  1  1  0  0  0
 32 41  1  6  0  0  0
 12 42  1  6  0  0  0
  7 43  1  1  0  0  0
  5 43  1  1  0  0  0
  3 44  1  0  0  0  0
  3 45  1  0  0  0  0
  2 46  1  1  0  0  0
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 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 47 52  1  0  0  0  0
 52 53  1  1  0  0  0
 54 53  1  1  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 54 59  1  0  0  0  0
 57 60  1  1  0  0  0
 56 61  1  1  0  0  0
 55 62  1  6  0  0  0
 51 63  1  6  0  0  0
 50 64  1  1  0  0  0
M  END

     RDKit          3D

142149  0  0  0  0  0  0  0  0999 V2000
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   -6.7141    3.5171    1.7696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6786    3.6202    0.3932 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.5482    3.5824    1.6074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4494    5.0700    0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652304282220382D          

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M  END
> <DATABASE_ID>
NP0073377

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H](CC[C@@H](O)C(C)(C)O)[C@H]1[C@H](C[C@@]2(C)[C@@H]3C[C@H](O)[C@@H]4[C@]5(C[C@@]35CC[C@]12C)CC[C@H](O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@H](O)[C@H](O)[C@H]1O)C4(C)C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C46H78O18/c1-20(8-9-27(51)42(4,5)58)29-24(61-39-35(57)33(55)32(54)25(16-47)62-39)15-44(7)26-14-21(48)37-41(2,3)28(10-11-46(37)19-45(26,46)13-12-43(29,44)6)63-40-36(31(53)23(50)18-60-40)64-38-34(56)30(52)22(49)17-59-38/h20-40,47-58H,8-19H2,1-7H3/t20-,21+,22+,23-,24+,25-,26+,27-,28+,29+,30+,31+,32-,33+,34-,35-,36-,37+,38+,39-,40+,43-,44+,45+,46-/m1/s1

> <INCHI_KEY>
HOLYOOXYJNTQAV-BIPAVQNASA-N

> <FORMULA>
C46H78O18

> <MOLECULAR_WEIGHT>
919.112

> <EXACT_MASS>
918.518815672

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_ATOM_COUNT>
142

> <JCHEM_AVERAGE_POLARIZABILITY>
100.1884122874845

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
12

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4S,5S,6R)-2-{[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-6-{[(2S,3R,4S,5R)-4,5-dihydroxy-3-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]oxy}-15-[(2R,5R)-5,6-dihydroxy-6-methylheptan-2-yl]-9-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-14-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.39

> <JCHEM_LOGP>
-1.262143078333331

> <ALOGPS_LOGS>
-3.11

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.356842492323576

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.876057181016495

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5265806826167054

> <JCHEM_POLAR_SURFACE_AREA>
298.14

> <JCHEM_REFRACTIVITY>
222.88070000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.09e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4S,5S,6R)-2-{[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-6-{[(2S,3R,4S,5R)-4,5-dihydroxy-3-{[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy}oxan-2-yl]oxy}-15-[(2R,5R)-5,6-dihydroxy-6-methylheptan-2-yl]-9-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3}.0^{3,8}.0^{12,16}]octadecan-14-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -0.993  -0.363   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.516  -1.811   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.523  -2.988   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.993  -2.717   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.516  -1.269   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.523  -0.092   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.032  -0.998   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.025  -2.175   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.501  -3.624   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.985  -3.895   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.462  -5.343   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.541  -1.904   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.064  -0.456   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.071   0.722   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.555   0.451   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.736   0.930   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.603  -0.506   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.031  -1.985   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.756  -2.849   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.479  -2.508   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.751  -4.024   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      11.199  -4.547   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      11.470  -6.063   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.293  -7.056   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.844  -6.533   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.573  -5.017   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.125  -4.494   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       7.667  -7.526   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      10.564  -8.572   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      12.918  -6.587   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      13.189  -8.103   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       8.548   0.710   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.074   0.499   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.654  -0.927   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.180  -1.138   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.760  -2.564   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      11.333  -3.145   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      14.186  -1.984   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      13.340  -3.991   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      13.125   0.078   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       7.968   2.137   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.172  -3.399   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.039   0.179   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -1.665  -4.022   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -0.305  -4.513   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      -3.032  -2.082   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      -3.555  -3.531   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      -2.562  -4.708   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      -3.086  -6.156   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -4.602  -6.427   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      -5.594  -5.250   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -5.071  -3.802   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0      -6.064  -2.624   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0      -5.541  -1.176   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      -6.533   0.001   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      -6.010   1.450   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      -4.494   1.721   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      -3.501   0.544   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      -4.025  -0.905   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      -3.971   3.169   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      -7.003   2.627   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0      -8.049  -0.270   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0      -7.110  -5.521   0.000  0.00  0.00           O+0
HETATM   64  O   UNK     0      -5.125  -7.876   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   46                                                  
CONECT    3    2    4   44   45                                             
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7   43                                             
CONECT    6    5    1                                                       
CONECT    7    5    8   15   43                                             
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    8   13   19   42                                             
CONECT   13   12   14   16   17                                             
CONECT   14   13   15                                                       
CONECT   15   14    7                                                       
CONECT   16   13                                                            
CONECT   17   13   18   32                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18   12                                                       
CONECT   20   18   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   30                                                  
CONECT   24   23   25   29                                                  
CONECT   25   24   26   28                                                  
CONECT   26   25   21   27                                                  
CONECT   27   26                                                            
CONECT   28   25                                                            
CONECT   29   24                                                            
CONECT   30   23   31                                                       
CONECT   31   30                                                            
CONECT   32   17   33   41                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   40                                                  
CONECT   36   35   37   38   39                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   36                                                            
CONECT   40   35                                                            
CONECT   41   32                                                            
CONECT   42   12                                                            
CONECT   43    7    5                                                       
CONECT   44    3                                                            
CONECT   45    3                                                            
CONECT   46    2   47                                                       
CONECT   47   46   48   52                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51   64                                                  
CONECT   51   50   52   63                                                  
CONECT   52   51   47   53                                                  
CONECT   53   52   54                                                       
CONECT   54   53   55   59                                                  
CONECT   55   54   56   62                                                  
CONECT   56   55   57   61                                                  
CONECT   57   56   58   60                                                  
CONECT   58   57   59                                                       
CONECT   59   58   54                                                       
CONECT   60   57                                                            
CONECT   61   56                                                            
CONECT   62   55                                                            
CONECT   63   51                                                            
CONECT   64   50                                                            
MASTER        0    0    0    0    0    0    0    0   64    0  142    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₆H₇₈O₁₈

Average Mass

919.1120 Da

Monoisotopic Mass

918.51882 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@H](CC[C@@H](O)C(C)(C)O)[C@H]1[C@H](C[C@@]2(C)[C@@H]3C[C@H](O)[C@@H]4[C@]5(C[C@@]35CC[C@]12C)CC[C@H](O[C@@H]1OC[C@@H](O)[C@H](O)[C@H]1O[C@@H]1OC[C@H](O)[C@H](O)[C@H]1O)C4(C)C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O

InChI Identifier

InChI=1S/C46H78O18/c1-20(8-9-27(51)42(4,5)58)29-24(61-39-35(57)33(55)32(54)25(16-47)62-39)15-44(7)26-14-21(48)37-41(2,3)28(10-11-46(37)19-45(26,46)13-12-43(29,44)6)63-40-36(31(53)23(50)18-60-40)64-38-34(56)30(52)22(49)17-59-38/h20-40,47-58H,8-19H2,1-7H3/t20-,21+,22+,23-,24+,25-,26+,27-,28+,29+,30+,31+,32-,33+,34-,35-,36-,37+,38+,39-,40+,43-,44+,45+,46-/m1/s1

InChI Key

HOLYOOXYJNTQAV-BIPAVQNASA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Astragalus campylosema Boiss. ssp. campylosema	Plant	KNApSAcK
Astragalus pendulus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cucurbitacin glycosides. These are polycyclic compounds containing a carbohydrate derivative glycosidically linked to a curcubitane nucleus.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroidal glycosides

Direct Parent

Cucurbitacin glycosides

Alternative Parents

Substituents

Cucurbitacin glycoside skeleton
Triterpene saponin
Triterpene glycoside
Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Triterpenoid
Cycloartane-skeleton
Trihydroxy bile acid, alcohol, or derivatives
25-hydroxysteroid
24-hydroxysteroid
Hydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
6-hydroxysteroid
Hydroxysteroid
O-glycosyl compound
Glycosyl compound
Disaccharide
Oxane
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Alcohol
Primary alcohol
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	-0.39	ALOGPS
logP	-1.3	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	11.88	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	12	ChemAxon
Polar Surface Area	298.14 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	222.88 m³·mol⁻¹	ChemAxon
Polarizability	100.19 Å³	ChemAxon
Number of Rings	8	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

162987265

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Askendoside G (NP0073377)

MOL for NP0073377 (Askendoside G)

3D MOL for NP0073377 (Askendoside G)

3D SDF for NP0073377 (Askendoside G)

3D-SDF for NP0073377 (Askendoside G)

PDB for NP0073377 (Askendoside G)

3D PDB for NP0073377 (Askendoside G)

SMILES for NP0073377 (Askendoside G)

INCHI for NP0073377 (Askendoside G)

Structure for NP0073377 (Askendoside G)

3D Structure for NP0073377 (Askendoside G)