NP-MRD: Showing NP-Card for 4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one (NP0302446)

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Record Information

Version

2.0

Created at

2022-09-10 16:01:12 UTC

Updated at

2022-09-10 16:01:12 UTC

NP-MRD ID

NP0302446

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one

Description

4-(8-{[4,5-Dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-dodecahydro-1H-naphtho[2,1-c]pyran-2-yl)-2,5-dihydrofuran-2-one belongs to the class of organic compounds known as diterpene glycosides. These are diterpenoids in which an isoprene unit is glycosylated. 4-(8-{[4,5-Dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-dodecahydro-1H-naphtho[2,1-c]pyran-2-yl)-2,5-dihydrofuran-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251513022D          

 46 51  0  0  0  0            999 V2000
   -5.0605   -0.6336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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 18 68  1  6
 19 69  1  0
 17 67  1  1
 16 65  1  0
 16 66  1  0
 15 63  1  0
 15 64  1  0
 14 62  1  1
 31 77  1  0
 31 78  1  0
 31 79  1  0
 32 80  1  0
 32 81  1  0
 32 82  1  0
 23 71  1  0
 27 72  1  0
 27 73  1  0
 41 91  1  1
 42 92  1  0
 43 93  1  6
 44 94  1  0
 45 95  1  1
 46 96  1  0
M  END


  Mrv1533004251513022D          

 46 51  0  0  0  0            999 V2000
   -5.0605   -0.6336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6480   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8230   -1.3480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855   -0.6336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105   -0.6336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5855    0.7954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    0.0809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    0.7954    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.7954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -0.6336    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.3480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -3.4914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.4914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2732   -3.6015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3977   -3.2142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -0.6336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6789    0.1201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2920    0.6721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2058    1.4926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0065    0.2596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8350   -0.5473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8230   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4105   -3.4914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6480   -2.7770    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0605   -3.4914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0605   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8855   -2.0625    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
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 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
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 22 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
 20 31  1  0  0  0  0
 31 32  1  0  0  0  0
 17 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 24 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 35 40  1  0  0  0  0
  4 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
  2 45  1  0  0  0  0
 45 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0302446

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2C(O)C(O)C(CO)OC2OC2CCC3(C)C4CC(OC(O)C4CCC3C2(C)C)C2=CC(=O)OC2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C32H50O14/c1-13-22(35)24(37)26(39)29(42-13)46-27-25(38)23(36)18(11-33)44-30(27)45-20-7-8-32(4)16-10-17(14-9-21(34)41-12-14)43-28(40)15(16)5-6-19(32)31(20,2)3/h9,13,15-20,22-30,33,35-40H,5-8,10-12H2,1-4H3

> <INCHI_KEY>
NLCPEJWMTDRXDL-UHFFFAOYSA-N

> <FORMULA>
C32H50O14

> <MOLECULAR_WEIGHT>
658.738

> <EXACT_MASS>
658.32005629

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_ATOM_COUNT>
96

> <JCHEM_AVERAGE_POLARIZABILITY>
68.62354750438972

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-dodecahydro-1H-naphtho[2,1-c]pyran-2-yl)-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
-0.91

> <JCHEM_LOGP>
-0.18771535099999936

> <ALOGPS_LOGS>
-2.72

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.830600104454394

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.683859169566703

> <JCHEM_PKA_STRONGEST_BASIC>
-2.98108376939566

> <JCHEM_POLAR_SURFACE_AREA>
214.05999999999997

> <JCHEM_REFRACTIVITY>
156.1668

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.26e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1H-naphtho[2,1-c]pyran-2-yl)-5H-furan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -9.446  -1.183   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.676  -2.516   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -7.136  -2.516   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      -6.366  -3.850   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -4.826  -3.850   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -4.056  -2.516   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.826  -1.183   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -6.366  -1.183   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -4.056   0.151   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.826   1.485   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.516   0.151   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.746   1.485   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.206   1.485   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      -1.746  -1.183   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.516  -2.516   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.746  -3.850   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -0.206  -3.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.564  -2.516   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.104  -2.516   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.874  -3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.644  -2.516   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.414  -3.850   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.184  -2.516   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.724  -2.516   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       7.494  -3.850   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.724  -5.184   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.494  -6.517   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.184  -5.184   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.414  -6.517   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.874  -6.517   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.104  -5.184   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.564  -5.184   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.510  -6.723   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.742  -6.000   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.494  -1.183   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.867   0.224   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.012   1.255   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       7.851   2.786   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       9.345   0.485   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       9.025  -1.022   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -7.136  -5.184   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      -6.366  -6.517   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      -8.676  -5.184   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -9.446  -6.517   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      -9.446  -3.850   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0     -10.986  -3.850   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   45                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   41                                                  
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   32                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   31                                             
CONECT   21   20                                                            
CONECT   22   20   23   28                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   35                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   22   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   20   32                                                  
CONECT   32   31   17   33   34                                             
CONECT   33   32                                                            
CONECT   34   32                                                            
CONECT   35   24   36   40                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   35                                                       
CONECT   41    4   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43    2   46                                                  
CONECT   46   45                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₅₀O₁₄

Average Mass

658.7380 Da

Monoisotopic Mass

658.32006 Da

IUPAC Name

4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-dodecahydro-1H-naphtho[2,1-c]pyran-2-yl)-2,5-dihydrofuran-2-one

Traditional Name

4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1H-naphtho[2,1-c]pyran-2-yl)-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

CC1OC(OC2C(O)C(O)C(CO)OC2OC2CCC3(C)C4CC(OC(O)C4CCC3C2(C)C)C2=CC(=O)OC2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C32H50O14/c1-13-22(35)24(37)26(39)29(42-13)46-27-25(38)23(36)18(11-33)44-30(27)45-20-7-8-32(4)16-10-17(14-9-21(34)41-12-14)43-28(40)15(16)5-6-19(32)31(20,2)3/h9,13,15-20,22-30,33,35-40H,5-8,10-12H2,1-4H3

InChI Key

NLCPEJWMTDRXDL-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
Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Naphthopyran
Disaccharide
Glycosyl compound
O-glycosyl compound
Naphthalene
Pyran
2-furanone
Oxane
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Secondary alcohol
Carboxylic acid ester
Hemiacetal
Lactone
Organoheterocyclic compound
Oxacycle
Polyol
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Acetal
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Primary alcohol
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	-0.91	ALOGPS
logP	-0.19	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	5.68	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	214.06 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	156.17 m³·mol⁻¹	ChemAxon
Polarizability	68.62 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

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

74941381

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one (NP0302446)

MOL for NP0302446 (4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one)

3D MOL for NP0302446 (4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one)

3D SDF for NP0302446 (4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one)

3D-SDF for NP0302446 (4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one)

PDB for NP0302446 (4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one)

3D PDB for NP0302446 (4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one)

SMILES for NP0302446 (4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one)

INCHI for NP0302446 (4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one)

Structure for NP0302446 (4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one)

3D Structure for NP0302446 (4-(8-{[4,5-dihydroxy-6-(hydroxymethyl)-3-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxy}-4-hydroxy-7,7,10a-trimethyl-decahydro-1h-naphtho[2,1-c]pyran-2-yl)-5h-furan-2-one)