NP-MRD: Showing NP-Card for 6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one (NP0302253)

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Record Information

Version

2.0

Created at

2022-09-10 15:40:42 UTC

Updated at

2022-09-10 15:40:42 UTC

NP-MRD ID

NP0302253

Secondary Accession Numbers

None

Natural Product Identification

Common Name

6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one

Description

6-[4-({3,4-Dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-octahydro-1H-inden-4-one belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. Based on a literature review very few articles have been published on 6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-octahydro-1H-inden-4-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102217402D          

 54 57  0  0  0  0            999 V2000
    4.9279   -3.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -3.0146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5549    0.2900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    0.8555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    2.1904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8946    1.9642    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5072    2.6351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3317    2.6063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7689    3.3059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3816    4.0344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5934    3.2771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9807    2.5487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8052    2.5199    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1925    1.7915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7554    1.0918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0170    1.7627    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0306    3.9768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8551    3.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2424    3.2196    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0669    3.1908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4542    2.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.2787    2.4335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6660    1.7051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2289    1.0055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4905    1.6763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8778    0.9479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.9277    2.3760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7522    2.3472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.5404    3.1044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9776    3.8040    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1168    4.6188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5540    5.3185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2923    4.6476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9050    5.3761    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  2  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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
 10 11  1  4  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 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
 14 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
 11 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 25 24  1  4  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 28 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
 41 49  1  0  0  0  0
 49 50  1  0  0  0  0
 39 51  1  0  0  0  0
 51 52  1  0  0  0  0
 51 53  1  0  0  0  0
 35 53  1  0  0  0  0
 53 54  1  0  0  0  0
M  END

     RDKit          3D

122125  0  0  0  0  0  0  0  0999 V2000
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 46114  1  0
M  END


  Mrv1652309102217402D          

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 35 53  1  0  0  0  0
 53 54  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0302253

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC(OC2C(C)OC(OC(CC=C(C)C)C(C)=CCC3(O)C(C)C4CCCC4(C)C(=O)C3C=C(C)C(O)CC=C(C)C)C(O)C2O)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C42H68O12/c1-21(2)13-15-30(43)24(6)20-29-38(49)41(10)18-11-12-28(41)25(7)42(29,50)19-17-23(5)31(16-14-22(3)4)53-39-36(48)34(46)37(27(9)52-39)54-40-35(47)33(45)32(44)26(8)51-40/h13-14,17,20,25-37,39-40,43-48,50H,11-12,15-16,18-19H2,1-10H3

> <INCHI_KEY>
IPNCRIZBOSAWLA-UHFFFAOYSA-N

> <FORMULA>
C42H68O12

> <MOLECULAR_WEIGHT>
764.994

> <EXACT_MASS>
764.47107763

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
122

> <JCHEM_AVERAGE_POLARIZABILITY>
86.08706916768699

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-octahydro-1H-inden-4-one

> <JCHEM_LOGP>
4.286412752666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.360926889836225

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.879906090964043

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3813110279120413

> <JCHEM_POLAR_SURFACE_AREA>
195.6

> <JCHEM_REFRACTIVITY>
205.97070000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one

> <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       9.199  -5.627   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.865  -4.857   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.531  -5.627   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.865  -3.317   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.531  -2.547   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.531  -1.007   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.865  -0.237   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.198  -0.237   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.864  -1.007   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.198   1.303   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.864   2.073   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.530   1.303   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.530  -0.237   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.197   2.073   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.036   0.541   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.268   1.597   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.173   2.843   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.268   4.089   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.197   3.613   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.530   4.383   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.530   5.923   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.864   3.613   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.403   3.667   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.680   4.919   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.219   4.865   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.035   6.171   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.312   7.531   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.574   6.117   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.297   4.758   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.836   4.704   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      11.559   3.344   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      10.743   2.038   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.098   3.290   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       9.390   7.423   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      10.930   7.370   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      11.653   6.010   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      13.192   5.956   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      13.915   4.596   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      14.008   7.262   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      15.547   7.208   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      16.270   5.849   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0      15.454   4.543   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      16.177   3.183   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      15.361   1.877   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      17.716   3.129   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0      18.439   1.769   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      18.532   4.435   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      20.071   4.381   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      17.809   5.795   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      18.625   7.101   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      13.285   8.622   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      14.101   9.928   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      11.746   8.676   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      11.023  10.035   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   22                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   19                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   11   23   24                                             
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   28   35                                                       
CONECT   35   34   36   53                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   51                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   49                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   41   50                                                  
CONECT   50   49                                                            
CONECT   51   39   52   53                                                  
CONECT   52   51                                                            
CONECT   53   51   35   54                                                  
CONECT   54   53                                                            
MASTER        0    0    0    0    0    0    0    0   54    0  114    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₆₈O₁₂

Average Mass

764.9940 Da

Monoisotopic Mass

764.47108 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1OC(OC2C(C)OC(OC(CC=C(C)C)C(C)=CCC3(O)C(C)C4CCCC4(C)C(=O)C3C=C(C)C(O)CC=C(C)C)C(O)C2O)C(O)C(O)C1O

InChI Identifier

InChI=1S/C42H68O12/c1-21(2)13-15-30(43)24(6)20-29-38(49)41(10)18-11-12-28(41)25(7)42(29,50)19-17-23(5)31(16-14-22(3)4)53-39-36(48)34(46)37(27(9)52-39)54-40-35(47)33(45)32(44)26(8)51-40/h13-14,17,20,25-37,39-40,43-48,50H,11-12,15-16,18-19H2,1-10H3

InChI Key

IPNCRIZBOSAWLA-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 triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Disaccharide
Glycosyl compound
O-glycosyl compound
Fatty acyl
Oxane
Cyclic alcohol
Tertiary alcohol
Secondary alcohol
Ketone
Acetal
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Alcohol
Organic oxygen compound
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source

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

73999956

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one (NP0302253)

MOL for NP0302253 (6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one)

3D MOL for NP0302253 (6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one)

3D SDF for NP0302253 (6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one)

3D-SDF for NP0302253 (6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one)

PDB for NP0302253 (6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one)

3D PDB for NP0302253 (6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one)

SMILES for NP0302253 (6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one)

INCHI for NP0302253 (6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one)

Structure for NP0302253 (6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one)

3D Structure for NP0302253 (6-[4-({3,4-dihydroxy-6-methyl-5-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}oxy)-3,7-dimethylocta-2,6-dien-1-yl]-6-hydroxy-5-(3-hydroxy-2,6-dimethylhepta-1,5-dien-1-yl)-3a,7-dimethyl-hexahydroinden-4-one)