NP-MRD: Showing NP-Card for 2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol (NP0249640)

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Record Information

Version

2.0

Created at

2022-09-07 12:15:12 UTC

Updated at

2022-09-07 12:15:12 UTC

NP-MRD ID

NP0249640

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol

Description

2-[(4,5-Dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]Hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated. 2-[(4,5-Dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]Hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241514242D          

 44 49  0  0  0  0            999 V2000
    8.8654   -0.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1702    0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4379   -0.3465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7427    0.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0104   -0.2824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9734   -1.1065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6686   -1.5507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4009   -1.1707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6316   -2.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3268   -2.8190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8993   -2.7549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8623   -3.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2041   -2.3107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2411   -1.4865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5459   -1.0424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.2474    0.1857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.0845    1.3660    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5120    1.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5490    2.1260    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2072    0.8577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9395    1.2377    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  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
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  6 15  1  0  0  0  0
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 28 38  1  0  0  0  0
  4 39  1  0  0  0  0
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 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
  2 43  1  0  0  0  0
 43 44  1  0  0  0  0
M  END

     RDKit          3D

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 27 79  1  0
 28 80  1  0
 28 81  1  0
 29 82  1  0
 19 69  1  0
 19 70  1  0
 18 67  1  0
 18 68  1  0
 17 66  1  1
 39 93  1  1
 40 94  1  0
 41 95  1  1
 42 96  1  0
 43 97  1  1
 44 98  1  0
M  END


  Mrv1533004241514242D          

 44 49  0  0  0  0            999 V2000
    8.8654   -0.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1702    0.0335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4379   -0.3465    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7427    0.0977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0104   -0.2824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9734   -1.1065    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6686   -1.5507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4009   -1.1707    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6316   -2.3748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3268   -2.8190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8993   -2.7549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8623   -3.5790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1300   -3.9590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2041   -2.3107    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2411   -1.4865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5459   -1.0424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8136   -1.4224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1184   -0.9782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8017   -1.7400    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6765   -0.3707    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4294    0.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6242    0.5960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0661   -0.0115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8257    0.7777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3132   -0.7987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7596   -1.4229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9506   -1.2543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6469   -0.4671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1726    0.0666    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4028    0.5335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1586    1.1914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0038    1.0309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2474    0.1857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7854   -0.2403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4825    0.2009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2972   -0.8873    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9928   -1.6541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1637   -0.8483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7797    0.9218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0845    1.3660    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5120    1.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5490    2.1260    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.2072    0.8577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9395    1.2377    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  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
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 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
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 18 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 23 33  1  0  0  0  0
 28 33  1  0  0  0  0
 30 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 34 38  1  0  0  0  0
 28 38  1  0  0  0  0
  4 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
  2 43  1  0  0  0  0
 43 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0249640

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2C(O)C(O)C(CO)OC2OCC2(C)CCCC3(C)C4CCC5CC4(CC5(O)CO)CCC23)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C32H54O12/c1-16-21(35)23(37)25(39)27(42-16)44-26-24(38)22(36)18(12-33)43-28(26)41-15-29(2)8-4-9-30(3)19(29)7-10-31-11-17(5-6-20(30)31)32(40,13-31)14-34/h16-28,33-40H,4-15H2,1-3H3

> <INCHI_KEY>
FMIIGEJYEBHNAS-UHFFFAOYSA-N

> <FORMULA>
C32H54O12

> <MOLECULAR_WEIGHT>
630.772

> <EXACT_MASS>
630.361527179

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
98

> <JCHEM_AVERAGE_POLARIZABILITY>
67.62280000656608

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol

> <ALOGPS_LOGP>
0.02

> <JCHEM_LOGP>
-0.17386569666666418

> <ALOGPS_LOGS>
-2.85

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.686605546091297

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.08912289581348

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810836384068518

> <JCHEM_POLAR_SURFACE_AREA>
198.76

> <JCHEM_REFRACTIVITY>
154.1523

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.94e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      16.549  -0.766   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      15.251   0.063   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      13.884  -0.647   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      12.586   0.182   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      11.219  -0.527   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      11.150  -2.066   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.448  -2.895   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      13.815  -2.185   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      12.379  -4.433   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      13.677  -5.262   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      11.012  -5.142   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.943  -6.681   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.576  -7.390   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       9.714  -4.313   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       9.783  -2.775   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.486  -1.946   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.119  -2.655   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.821  -1.826   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.230  -3.248   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.863  -0.692   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.402   0.777   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.899   1.113   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.857  -0.022   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.408   1.452   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.318  -1.491   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.285  -2.656   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.774  -2.341   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.208  -0.872   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.322   0.124   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.752   0.996   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.296   2.224   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.874   1.924   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.328   0.347   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -1.466  -0.449   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -2.767   0.375   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -2.422  -1.656   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -1.853  -3.088   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -0.306  -1.583   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      12.655   1.721   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      11.358   2.550   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      14.022   2.430   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      14.091   3.969   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      15.320   1.601   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      16.687   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   43                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   39                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14    6   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   25                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25   33                                             
CONECT   24   23                                                            
CONECT   25   23   18   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   33   38                                             
CONECT   29   28   30                                                       
CONECT   30   29   31   34                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   23   28                                                  
CONECT   34   30   35   36   38                                             
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36                                                            
CONECT   38   34   28                                                       
CONECT   39    4   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41    2   44                                                  
CONECT   44   43                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₅₄O₁₂

Average Mass

630.7720 Da

Monoisotopic Mass

630.36153 Da

IUPAC Name

2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol

Traditional Name

2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

CC1OC(OC2C(O)C(O)C(CO)OC2OCC2(C)CCCC3(C)C4CCC5CC4(CC5(O)CO)CCC23)C(O)C(O)C1O

InChI Identifier

InChI=1S/C32H54O12/c1-16-21(35)23(37)25(39)27(42-16)44-26-24(38)22(36)18(12-33)43-28(26)41-15-29(2)8-4-9-30(3)19(29)7-10-31-11-17(5-6-20(30)31)32(40,13-31)14-34/h16-28,33-40H,4-15H2,1-3H3

InChI Key

FMIIGEJYEBHNAS-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Diterpene glycosides

Alternative Parents

Substituents

Diterpene glycoside
Diterpenoid
Kaurane diterpenoid
Disaccharide
Glycosyl compound
O-glycosyl compound
Oxane
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Polyol
Oxacycle
Acetal
Organoheterocyclic compound
Primary alcohol
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Alcohol
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	0.02	ALOGPS
logP	-0.17	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	12.09	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	198.76 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	154.15 m³·mol⁻¹	ChemAxon
Polarizability	67.62 Å³	ChemAxon
Number of Rings	6	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

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DrugBank ID

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Phenol Explorer Compound ID

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FoodDB ID

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KNApSAcK ID

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Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

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PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for 2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol (NP0249640)

MOL for NP0249640 (2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol)

3D MOL for NP0249640 (2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol)

3D SDF for NP0249640 (2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol)

3D-SDF for NP0249640 (2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol)

PDB for NP0249640 (2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol)

3D PDB for NP0249640 (2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol)

SMILES for NP0249640 (2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol)

INCHI for NP0249640 (2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol)

Structure for NP0249640 (2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol)

3D Structure for NP0249640 (2-[(4,5-dihydroxy-2-{[14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadecan-5-yl]methoxy}-6-(hydroxymethyl)oxan-3-yl)oxy]-6-methyloxane-3,4,5-triol)