NP-MRD: Showing NP-Card for [7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate (NP0226975)

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Record Information

Version

2.0

Created at

2022-09-06 06:10:30 UTC

Updated at

2022-09-06 06:10:30 UTC

NP-MRD ID

NP0226975

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate

Description

[7-(Acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]methyl acetate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. [7-(Acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]methyl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004171519512D          

 40 42  0  0  0  0            999 V2000
   -2.1671   -9.1113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3133   -8.2993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6833   -7.7667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8295   -6.9548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1995   -6.4222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4232   -6.7015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3457   -5.6102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7157   -5.0776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8619   -4.2657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2319   -3.7331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -2.9211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2519   -2.3885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1913   -1.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5099   -1.1311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9551   -1.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4877   -1.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3123   -1.9097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9223   -1.1827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7469   -1.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5715   -1.2342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9615   -1.9612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7861   -1.9870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1761   -2.7140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0007   -2.7397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7415   -3.4152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -2.6624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2930   -2.9687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3583   -3.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5747   -3.7279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4061   -4.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0212   -5.0852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6224   -4.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7023   -2.6367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2677   -3.3379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4431   -3.3122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0531   -2.5852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5476   -3.2371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1544   -2.6418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1220   -5.3309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0896   -8.0200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 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
 17 19  1  0  0  0  0
 19 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  2  0  0  0  0
 23 25  1  0  0  0  0
 21 26  1  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
 30 32  1  0  0  0  0
 26 33  1  0  0  0  0
 17 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 12 36  1  0  0  0  0
 16 36  1  0  0  0  0
 36 37  1  0  0  0  0
 11 38  1  4  0  0  0
  7 39  1  0  0  0  0
  2 40  1  0  0  0  0
M  END


  Mrv1533004171519512D          

 40 42  0  0  0  0            999 V2000
   -2.1671   -9.1113    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3133   -8.2993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6833   -7.7667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8295   -6.9548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1995   -6.4222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4232   -6.7015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3457   -5.6102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7157   -5.0776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8619   -4.2657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2319   -3.7331    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3781   -2.9211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2519   -2.3885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1913   -1.5657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5099   -1.1311    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9551   -1.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4877   -1.8839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3123   -1.9097    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9223   -1.1827    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7469   -1.2084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5715   -1.2342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9615   -1.9612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7861   -1.9870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1761   -2.7140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0007   -2.7397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7415   -3.4152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5269   -2.6624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2930   -2.9687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3583   -3.4700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5747   -3.7279    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4061   -4.5355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0212   -5.0852    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6224   -4.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7023   -2.6367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2677   -3.3379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4431   -3.3122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0531   -2.5852    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5476   -3.2371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1544   -2.6418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1220   -5.3309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0896   -8.0200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  4  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 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
 17 19  1  0  0  0  0
 19 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  2  0  0  0  0
 23 25  1  0  0  0  0
 21 26  1  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
 30 32  1  0  0  0  0
 26 33  1  0  0  0  0
 17 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 12 36  1  0  0  0  0
 16 36  1  0  0  0  0
 36 37  1  0  0  0  0
 11 38  1  4  0  0  0
  7 39  1  0  0  0  0
  2 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0226975

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC(O)C(C)=CC=CC(C)=C1C(=O)CC2C1(C)CCC1C(C)(COC(C)=O)C(CCC21C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C34H50O6/c1-21(2)13-14-26(37)22(3)11-10-12-23(4)31-27(38)19-29-32(7)18-16-30(40-25(6)36)34(9,20-39-24(5)35)28(32)15-17-33(29,31)8/h10-13,26,28-30,37H,14-20H2,1-9H3

> <INCHI_KEY>
FDRWOTSJMOAODM-UHFFFAOYSA-N

> <FORMULA>
C34H50O6

> <MOLECULAR_WEIGHT>
554.768

> <EXACT_MASS>
554.36073933

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
63.70326645386681

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]methyl acetate

> <ALOGPS_LOGP>
6.58

> <JCHEM_LOGP>
5.408353634999999

> <ALOGPS_LOGS>
-5.79

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.77490923802437

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.27204445131122

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3674582358221352

> <JCHEM_POLAR_SURFACE_AREA>
89.9

> <JCHEM_REFRACTIVITY>
160.77820000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.06e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      -4.045 -17.008   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.318 -15.492   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.142 -14.498   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.415 -12.982   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.239 -11.988   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.790 -12.509   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.512 -10.472   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.336  -9.478   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.609  -7.963   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.433  -6.968   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.706  -5.453   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.470  -4.459   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.357  -2.923   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -0.952  -2.111   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.783  -2.341   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.777  -3.517   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.316  -3.565   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.588  -2.208   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.128  -2.256   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.667  -2.304   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.395  -3.661   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.934  -3.709   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.662  -5.066   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.201  -5.114   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.851  -6.375   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.584  -4.970   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.014  -5.542   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.269  -6.477   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.806  -6.959   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.491  -8.466   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.640  -9.492   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       3.029  -8.947   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.044  -4.922   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.233  -6.231   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.694  -6.183   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.966  -4.826   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.022  -6.043   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -2.155  -4.931   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -3.961  -9.951   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -5.767 -14.971   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   40                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   39                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   38                                                  
CONECT   12   11   13   36                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17   36                                                  
CONECT   17   16   18   19   33                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21   27   28   33                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   26   17   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   12   16   37                                             
CONECT   37   36                                                            
CONECT   38   11                                                            
CONECT   39    7                                                            
CONECT   40    2                                                            
MASTER        0    0    0    0    0    0    0    0   40    0   84    0
END

View in JSmol

Synonyms

Value	Source
[7-(Acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]methyl acetic acid	Generator

Chemical Formula

C₃₄H₅₀O₆

Average Mass

554.7680 Da

Monoisotopic Mass

554.36074 Da

IUPAC Name

[7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-dodecahydro-1H-cyclopenta[a]naphthalen-6-yl]methyl acetate

Traditional Name

[7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(C)=CCC(O)C(C)=CC=CC(C)=C1C(=O)CC2C1(C)CCC1C(C)(COC(C)=O)C(CCC21C)OC(C)=O

InChI Identifier

InChI=1S/C34H50O6/c1-21(2)13-14-26(37)22(3)11-10-12-23(4)31-27(38)19-29-32(7)18-16-30(40-25(6)36)34(9,20-39-24(5)35)28(32)15-17-33(29,31)8/h10-13,26,28-30,37H,14-20H2,1-9H3

InChI Key

FDRWOTSJMOAODM-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 alcohol
Dicarboxylic acid or derivatives
Fatty acyl
Carboxylic acid ester
Ketone
Secondary alcohol
Cyclic ketone
Carboxylic acid derivative
Organic oxide
Organic oxygen compound
Alcohol
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	6.58	ALOGPS
logP	5.41	ChemAxon
logS	-5.8	ALOGPS
pKa (Strongest Acidic)	18.27	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	89.9 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	160.78 m³·mol⁻¹	ChemAxon
Polarizability	63.7 Å³	ChemAxon
Number of Rings	3	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

73999866

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate (NP0226975)

MOL for NP0226975 ([7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate)

3D MOL for NP0226975 ([7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate)

3D SDF for NP0226975 ([7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate)

3D-SDF for NP0226975 ([7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate)

PDB for NP0226975 ([7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate)

3D PDB for NP0226975 ([7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate)

SMILES for NP0226975 ([7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate)

INCHI for NP0226975 ([7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate)

Structure for NP0226975 ([7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate)

3D Structure for NP0226975 ([7-(acetyloxy)-3-(7-hydroxy-6,10-dimethylundeca-3,5,9-trien-2-ylidene)-3a,6,9a-trimethyl-2-oxo-octahydrocyclopenta[a]naphthalen-6-yl]methyl acetate)