NP-MRD: Showing NP-Card for (3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0296465)

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Record Information

Version

2.0

Created at

2022-09-10 06:03:25 UTC

Updated at

2022-09-10 06:03:25 UTC

NP-MRD ID

NP0296465

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

Description

(3R,4S,5S,6R)-2-{[(2R,3R,4aR,5R,6aR,6bR,8S,10S,12aR,12bR,14aR)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-docosahydropicen-2-yl]oxy}-6-(hydroxymethyl)oxane-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. (3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol is found in Spergula fallax. Based on a literature review very few articles have been published on (3R,4S,5S,6R)-2-{[(2R,3R,4aR,5R,6aR,6bR,8S,10S,12aR,12bR,14aR)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-docosahydropicen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102208032D          

 54 60  0  0  1  0            999 V2000
   -0.4733   -5.5341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -5.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.1270   -5.2520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -5.9664    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1270   -6.6809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1895   -5.9664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9355   -4.5375    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  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  6  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 18 27  1  0  0  0  0
 27 28  1  1  0  0  0
 16 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 34 31  1  6  0  0  0
 14 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  1  0  0  0
 40 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 37 44  1  0  0  0  0
 44 45  1  6  0  0  0
 35 46  1  0  0  0  0
 46 47  1  0  0  0  0
 13 47  1  0  0  0  0
  8 47  1  0  0  0  0
 47 48  1  6  0  0  0
 10 49  1  0  0  0  0
  4 49  1  0  0  0  0
 49 50  1  1  0  0  0
 49 51  1  0  0  0  0
 51 52  1  0  0  0  0
 52 53  1  0  0  0  0
  2 53  1  0  0  0  0
 53 54  1  1  0  0  0
M  END

     RDKit          3D

122128  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309102208032D          

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M  END
> <DATABASE_ID>
NP0296465

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)[C@@H](O)CC[C@]2(C)[C@H]3CC[C@@H]4C5C[C@@H](OC6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)[C@H](O)C(C)(C)[C@@H]5[C@@H](C[C@@]4(C)[C@]3(C)C[C@H](O)C12)OC1OC[C@@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C40H68O14/c1-36(2)25(44)10-11-38(5)24-9-8-18-17-12-21(52-35-31(49)29(47)28(46)23(15-41)54-35)33(50)37(3,4)26(17)22(53-34-30(48)27(45)20(43)16-51-34)14-39(18,6)40(24,7)13-19(42)32(36)38/h17-35,41-50H,8-16H2,1-7H3/t17?,18-,19+,20-,21-,22-,23-,24-,25+,26+,27-,28-,29+,30+,31-,32?,33+,34?,35?,38-,39-,40-/m1/s1

> <INCHI_KEY>
NFVZLFIQCMHYIF-FXBGQQRRSA-N

> <FORMULA>
C40H68O14

> <MOLECULAR_WEIGHT>
772.97

> <EXACT_MASS>
772.46090687

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
122

> <JCHEM_AVERAGE_POLARIZABILITY>
84.35413378679107

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
10

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R,4S,5S,6R)-2-{[(2R,3R,4aR,5R,6aR,6bR,8S,10S,12aR,12bR,14aR)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-docosahydropicen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_LOGP>
-0.32590742166666764

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.444465350123295

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.920528384168101

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810835533279123

> <JCHEM_POLAR_SURFACE_AREA>
239.21999999999994

> <JCHEM_REFRACTIVITY>
191.50830000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4S,5S,6R)-2-{[(2R,3R,4aR,5R,6aR,6bR,8S,10S,12aR,12bR,14aR)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1H-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.883 -10.330   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.564  -9.804   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.831 -11.320   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.104  -9.804   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.874 -11.137   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.104 -12.471   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.414 -11.137   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.184  -9.804   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.954 -11.137   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.414  -8.470   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.184  -7.136   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.724  -7.136   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.494  -8.470   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.034  -8.470   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.804  -7.136   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.344  -7.136   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      12.114  -5.803   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      11.344  -4.469   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.804  -4.469   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.034  -3.135   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.494  -3.135   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.724  -1.802   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.804  -1.802   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.034  -0.468   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      11.344  -1.802   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      12.114  -0.468   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      12.114  -3.135   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      13.654  -3.135   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      12.114  -8.470   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      13.654  -8.470   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      11.344  -9.804   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      12.791 -10.330   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.076 -11.320   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.804  -9.804   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.034 -11.137   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       9.804 -12.471   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       9.034 -13.805   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       9.804 -15.138   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       9.034 -16.472   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.494 -16.472   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       6.724 -17.806   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       6.724 -15.138   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       5.184 -15.138   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0       7.494 -13.805   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       6.724 -12.471   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       7.494 -11.137   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       6.724  -9.804   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       6.885 -11.335   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       2.874  -8.470   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       3.644  -7.136   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       2.104  -7.136   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       0.564  -7.136   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      -0.206  -8.470   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      -1.746  -8.470   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   53                                             
CONECT    3    2                                                            
CONECT    4    2    5   49                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10   47                                             
CONECT    9    8                                                            
CONECT   10    8   11   49                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   47                                                  
CONECT   14   13   15   34                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   29                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   27                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   18   28                                                  
CONECT   28   27                                                            
CONECT   29   16   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   33   34                                             
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   31   14   35                                                  
CONECT   35   34   36   46                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   44                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   37   45                                                  
CONECT   45   44                                                            
CONECT   46   35   47                                                       
CONECT   47   46   13    8   48                                             
CONECT   48   47                                                            
CONECT   49   10    4   50   51                                             
CONECT   50   49                                                            
CONECT   51   49   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52    2   54                                                  
CONECT   54   53                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  120    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₆₈O₁₄

Average Mass

772.9700 Da

Monoisotopic Mass

772.46091 Da

IUPAC Name

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1(C)[C@@H](O)CC[C@]2(C)[C@H]3CC[C@@H]4C5C[C@@H](OC6O[C@H](CO)[C@@H](O)[C@H](O)[C@H]6O)[C@H](O)C(C)(C)[C@@H]5[C@@H](C[C@@]4(C)[C@]3(C)C[C@H](O)C12)OC1OC[C@@H](O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C40H68O14/c1-36(2)25(44)10-11-38(5)24-9-8-18-17-12-21(52-35-31(49)29(47)28(46)23(15-41)54-35)33(50)37(3,4)26(17)22(53-34-30(48)27(45)20(43)16-51-34)14-39(18,6)40(24,7)13-19(42)32(36)38/h17-35,41-50H,8-16H2,1-7H3/t17?,18-,19+,20-,21-,22-,23-,24-,25+,26+,27-,28-,29+,30+,31-,32?,33+,34?,35?,38-,39-,40-/m1/s1

InChI Key

NFVZLFIQCMHYIF-FXBGQQRRSA-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
Spergula fallax	LOTUS Database	35616633

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
O-glycosyl compound
Glycosyl compound
Oxane
Monosaccharide
Cyclic alcohol
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
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	-0.33	ChemAxon
pKa (Strongest Acidic)	11.92	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	10	ChemAxon
Polar Surface Area	239.22 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	191.51 m³·mol⁻¹	ChemAxon
Polarizability	84.35 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

162975267

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol (NP0296465)

MOL for NP0296465 ((3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D MOL for NP0296465 ((3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D SDF for NP0296465 ((3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D-SDF for NP0296465 ((3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

PDB for NP0296465 ((3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D PDB for NP0296465 ((3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

SMILES for NP0296465 ((3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

INCHI for NP0296465 ((3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

Structure for NP0296465 ((3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)

3D Structure for NP0296465 ((3r,4s,5s,6r)-2-{[(2r,3r,4ar,5r,6ar,6br,8s,10s,12ar,12br,14ar)-3,8,10-trihydroxy-4,4,6a,6b,9,9,12a-heptamethyl-5-{[(3s,4r,5r)-3,4,5-trihydroxyoxan-2-yl]oxy}-hexadecahydro-1h-picen-2-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol)