NP-MRD: Showing NP-Card for 2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol (NP0230707)

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Record Information

Version

2.0

Created at

2022-09-06 11:14:37 UTC

Updated at

2022-09-06 11:14:38 UTC

NP-MRD ID

NP0230707

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

Description

AC1MWPG7 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. 2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol is found in Astragalus membranaceus. AC1MWPG7 is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004151519452D          

 66 74  0  0  0  0            999 V2000
    4.3428    4.1907    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9735    4.7226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4417    5.3533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7220    6.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1901    6.7599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4704    7.5358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9386    8.1665    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2189    8.9425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2826    7.6810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5629    8.4570    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8144    7.0503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6265    7.1955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3282    4.1514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6390    3.3872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0083    2.8554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6032    2.2837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5020    2.2041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7313    1.4116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5072    1.1313    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0484    0.9486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3971    1.4549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5850    1.3097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4002   -0.5326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0562   -0.0471    0.0000 C   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  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
  2 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
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 16 21  1  0  0  0  0
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 22 55  1  0  0  0  0
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 63 65  1  0  0  0  0
 58 65  1  0  0  0  0
 65 66  1  0  0  0  0
M  END

     RDKit          3D

144152  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004151519452D          

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M  END
> <DATABASE_ID>
NP0230707

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(OC1OC(CO)C(O)C(O)C1O)C1CCC(C)(O1)C1C(O)CC2(C)C3CC(OC4OC(CO)C(O)C(O)C4O)C4C5(CC35CCC12C)CCC(OC1OCC(O)C(O)C1O)C4(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C47H78O19/c1-41(2)26(64-38-33(57)28(52)21(51)18-60-38)9-11-47-19-46(47)13-12-43(5)36(45(7)10-8-27(65-45)42(3,4)66-40-35(59)32(56)30(54)24(17-49)63-40)20(50)15-44(43,6)25(46)14-22(37(41)47)61-39-34(58)31(55)29(53)23(16-48)62-39/h20-40,48-59H,8-19H2,1-7H3

> <INCHI_KEY>
YDELUYNKSQLCJK-UHFFFAOYSA-N

> <FORMULA>
C47H78O19

> <MOLECULAR_WEIGHT>
947.122

> <EXACT_MASS>
946.513730292

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_ATOM_COUNT>
144

> <JCHEM_AVERAGE_POLARIZABILITY>
99.57581868393204

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
12

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

> <ALOGPS_LOGP>
-0.46

> <JCHEM_LOGP>
-2.0823786759999985

> <ALOGPS_LOGS>
-3.02

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.202456907702944

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.757417683633046

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6483775345966762

> <JCHEM_POLAR_SURFACE_AREA>
307.36999999999995

> <JCHEM_REFRACTIVITY>
226.99340000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.01e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0       8.107   7.823   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.284   8.815   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.461   9.808   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       8.291   9.993   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.814  11.441   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.822  12.618   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.345  14.067   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.352  15.244   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.875  16.693   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.861  14.338   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.384  15.786   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.854  13.161   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      12.369  13.432   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.330  11.712   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      11.323  10.535   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      10.277   7.638   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.813   7.749   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.393   6.323   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.216   5.330   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.326   4.263   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.908   6.143   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.270   4.114   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.698   2.635   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.147   2.112   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.424   1.771   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.208   2.716   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.839   1.221   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.692   2.445   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.169   0.996   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.653   0.725   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.130  -0.723   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       2.614  -0.994   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       1.621   0.183   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       0.105  -0.088   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -0.888   1.089   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -2.404   0.818   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -0.418  -1.536   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -1.934  -1.807   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       0.574  -2.714   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       0.051  -4.162   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.090  -2.442   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       3.083  -3.620   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       3.660   1.903   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       2.144   1.632   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.674   0.186   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       0.812   0.858   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       1.151   2.809   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       1.675   4.257   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       3.191   4.528   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       4.183   3.351   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       4.707   4.799   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       5.699   3.622   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       6.222   5.071   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       7.738   5.342   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       8.731   4.164   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       9.403   5.550   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0      -0.365   2.538   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0      -1.357   3.715   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0      -2.873   3.444   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0      -3.866   4.621   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0      -3.343   6.070   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      -4.335   7.247   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0      -1.827   6.341   0.000  0.00  0.00           C+0
HETATM   64  O   UNK     0      -1.304   7.789   0.000  0.00  0.00           O+0
HETATM   65  C   UNK     0      -0.834   5.164   0.000  0.00  0.00           C+0
HETATM   66  O   UNK     0       0.682   5.435   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   16                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   14                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    5   15                                                  
CONECT   15   14                                                            
CONECT   16    2   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19   16                                                       
CONECT   22   19   23   55                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28   55                                             
CONECT   27   26                                                            
CONECT   28   26   29   52                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   43                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   41                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   37                                                  
CONECT   35   34   36                                                       
CONECT   36   35                                                            
CONECT   37   34   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   32   42                                                  
CONECT   42   41                                                            
CONECT   43   30   44   50                                                  
CONECT   44   43   45   46   47                                             
CONECT   45   44                                                            
CONECT   46   44                                                            
CONECT   47   44   48   57                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   43   51   52                                             
CONECT   51   50   52                                                       
CONECT   52   51   28   50   53                                             
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   22   26   56                                             
CONECT   56   55                                                            
CONECT   57   47   58                                                       
CONECT   58   57   59   65                                                  
CONECT   59   58   60                                                       
CONECT   60   59   61                                                       
CONECT   61   60   62   63                                                  
CONECT   62   61                                                            
CONECT   63   61   64   65                                                  
CONECT   64   63                                                            
CONECT   65   63   58   66                                                  
CONECT   66   65                                                            
MASTER        0    0    0    0    0    0    0    0   66    0  148    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₇H₇₈O₁₉

Average Mass

947.1220 Da

Monoisotopic Mass

946.51373 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(C)(OC1OC(CO)C(O)C(O)C1O)C1CCC(C)(O1)C1C(O)CC2(C)C3CC(OC4OC(CO)C(O)C(O)C4O)C4C5(CC35CCC12C)CCC(OC1OCC(O)C(O)C1O)C4(C)C

InChI Identifier

InChI=1S/C47H78O19/c1-41(2)26(64-38-33(57)28(52)21(51)18-60-38)9-11-47-19-46(47)13-12-43(5)36(45(7)10-8-27(65-45)42(3,4)66-40-35(59)32(56)30(54)24(17-49)63-40)20(50)15-44(43,6)25(46)14-22(37(41)47)61-39-34(58)31(55)29(53)23(16-48)62-39/h20-40,48-59H,8-19H2,1-7H3

InChI Key

YDELUYNKSQLCJK-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
Astragalus membranaceus	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
Cycloartane-skeleton
Triterpenoid
16-hydroxysteroid
Hydroxysteroid
Glycosyl compound
O-glycosyl compound
Monosaccharide
Oxane
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Oxacycle
Ether
Dialkyl ether
Acetal
Organoheterocyclic compound
Polyol
Organooxygen compound
Primary alcohol
Alcohol
Hydrocarbon derivative
Organic oxygen 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	-0.46	ALOGPS
logP	-2.1	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	11.76	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	19	ChemAxon
Hydrogen Donor Count	12	ChemAxon
Polar Surface Area	307.37 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	226.99 m³·mol⁻¹	ChemAxon
Polarizability	99.58 Å³	ChemAxon
Number of Rings	9	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

3752972

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol (NP0230707)

MOL for NP0230707 (2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0230707 (2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0230707 (2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0230707 (2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0230707 (2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0230707 (2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0230707 (2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0230707 (2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0230707 (2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0230707 (2-({2-[5-(14-hydroxy-7,7,12,16-tetramethyl-9-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-6-[(3,4,5-trihydroxyoxan-2-yl)oxy]pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl)-5-methyloxolan-2-yl]propan-2-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol)