NP-MRD: Showing NP-Card for 7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate (NP0285751)

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Record Information

Version

2.0

Created at

2022-09-09 14:03:22 UTC

Updated at

2022-09-09 14:03:22 UTC

NP-MRD ID

NP0285751

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate

Description

7-(Acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-3a,5a,9-trimethyl-1-(propan-2-yl)-1H,2H,3H,3aH,4H,5H,5aH,6H,7H,8H,10aH,10bH-cyclohepta[e]inden-4-yl 2-methylbutanoate belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. Based on a literature review very few articles have been published on 7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-3a,5a,9-trimethyl-1-(propan-2-yl)-1H,2H,3H,3aH,4H,5H,5aH,6H,7H,8H,10aH,10bH-cyclohepta[e]inden-4-yl 2-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092216032D          

 44 46  0  0  0  0            999 V2000
   -5.1722   -4.1011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3678   -3.9175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1247   -3.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3203   -2.9456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7592   -3.5503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0772   -2.1572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2729   -1.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6516   -2.5164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9434   -2.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8449   -2.9124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1550   -2.3365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0286   -3.1408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8169   -3.3840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4217   -2.8228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0005   -4.1883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3957   -4.7494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6684    1.7350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.5063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9486   -1.2150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3718   -0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1967   -0.5192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9700    0.2137    0.0000 C   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  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
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 22 40  1  0  0  0  0
  9 40  1  0  0  0  0
 40 41  1  0  0  0  0
  7 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
M  END

     RDKit          3D

100102  0  0  0  0  0  0  0  0999 V2000
   -6.7718    0.6389   -2.5419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1234    1.9094   -2.0122 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5227    1.6579   -0.6328 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.2568    0.0447   -1.9020 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.7767   -0.9195    0.1752 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2707   -2.0737    0.9529 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9507   -1.5989    2.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
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  1 45  1  0
  1 46  1  0
  1 47  1  0
 44 98  1  0
 44 99  1  0
 44100  1  0
 42 96  1  0
 42 97  1  0
 34 86  1  1
 38 87  1  6
 39 88  1  0
 39 89  1  0
 39 90  1  0
 40 91  1  0
 40 92  1  0
 41 93  1  0
 41 94  1  0
 41 95  1  0
M  END


  Mrv1652309092216032D          

 44 46  0  0  0  0            999 V2000
   -5.1722   -4.1011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3678   -3.9175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1247   -3.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3203   -2.9456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7592   -3.5503    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0772   -2.1572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2729   -1.9736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6516   -2.5164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9434   -2.0933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8449   -2.9124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1550   -2.3365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0286   -3.1408    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8169   -3.3840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4217   -2.8228    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0005   -4.1883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3957   -4.7494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7888   -4.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9724   -5.2358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4498   -1.7753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2662   -0.9710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0342   -1.2724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5222   -0.7278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8236    0.0401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4111    0.7546    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8758    1.4362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4047    0.8776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6479    1.6659    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0095    0.3164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7775    0.6178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9004    1.4336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2554    1.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6684    1.7350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -0.5063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6623   -0.9188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6623   -1.7438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9478   -2.1563    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3768   -2.1563    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0912   -1.7438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0912   -0.9188    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1269   -1.2890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9486   -1.2150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3718   -0.5068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1967   -0.5192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9700    0.2137    0.0000 C   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  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  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
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 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  2  0  0  0  0
 24 25  1  0  0  0  0
 24 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  1  0  0  0  0
 30 32  2  0  0  0  0
 28 33  1  0  0  0  0
 20 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 22 40  1  0  0  0  0
  9 40  1  0  0  0  0
 40 41  1  0  0  0  0
  7 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0285751

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)OC1CC2(C)C(C1C(C)C)C1C=C(C)C(O)C(OC(C)=O)C(OC(=O)CCC)C1(C)CC2OC(=O)C(C)CC

> <INCHI_IDENTIFIER>
InChI=1S/C35H56O9/c1-11-14-26(37)42-24-17-35(10)25(43-33(40)20(6)13-3)18-34(9)23(29(35)28(24)19(4)5)16-21(7)30(39)31(41-22(8)36)32(34)44-27(38)15-12-2/h16,19-20,23-25,28-32,39H,11-15,17-18H2,1-10H3

> <INCHI_KEY>
JCOUIOWVKORDDJ-UHFFFAOYSA-N

> <FORMULA>
C35H56O9

> <MOLECULAR_WEIGHT>
620.824

> <EXACT_MASS>
620.392433383

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
100

> <JCHEM_AVERAGE_POLARIZABILITY>
71.11562294406902

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-3a,5a,9-trimethyl-1-(propan-2-yl)-1H,2H,3H,3aH,4H,5H,5aH,6H,7H,8H,10aH,10bH-cyclohepta[e]inden-4-yl 2-methylbutanoate

> <JCHEM_LOGP>
6.144966713333334

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.515284987434946

> <JCHEM_PKA_STRONGEST_BASIC>
-3.448214346495954

> <JCHEM_POLAR_SURFACE_AREA>
125.43

> <JCHEM_REFRACTIVITY>
164.70370000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1H,2H,3H,4H,5H,6H,7H,8H,10aH,10bH-cyclohepta[e]inden-4-yl 2-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -9.655  -7.655   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.153  -7.313   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.699  -5.841   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -6.198  -5.498   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -5.151  -6.627   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      -5.744  -4.027   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -4.243  -3.684   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.083  -4.697   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.761  -3.908   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.577  -5.436   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.289  -4.361   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       0.053  -5.863   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       1.525  -6.317   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.654  -5.269   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.868  -7.818   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.739  -8.866   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.339  -8.272   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.682  -9.773   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.840  -3.314   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.497  -1.813   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.930  -2.375   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.975  -1.359   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.537   0.075   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.767   1.409   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.635   2.681   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.755   1.638   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.209   3.110   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.884   0.591   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       3.318   1.153   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.547   2.676   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.343   3.636   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       4.981   3.239   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.769  -0.945   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.103  -1.715   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       3.103  -3.255   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       1.769  -4.025   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       4.437  -4.025   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       5.770  -3.255   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.770  -1.715   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.104  -2.406   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -3.637  -2.268   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -4.427  -0.946   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -5.967  -0.969   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -3.677   0.399   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   41                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11   40                                             
CONECT   10    9                                                            
CONECT   11    9   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17                                                            
CONECT   19   11   20                                                       
CONECT   20   19   21   22   33                                             
CONECT   21   20                                                            
CONECT   22   20   23   40                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   28   20   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38                                                            
CONECT   40   22    9   41                                                  
CONECT   41   40    7   42                                                  
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   92    0
END

View in JSmol

Synonyms

Value	Source
7-(Acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-3a,5a,9-trimethyl-1-(propan-2-yl)-1H,2H,3H,3ah,4H,5H,5ah,6H,7H,8H,10ah,10BH-cyclohepta[e]inden-4-yl 2-methylbutanoic acid	Generator

Chemical Formula

C₃₅H₅₆O₉

Average Mass

620.8240 Da

Monoisotopic Mass

620.39243 Da

IUPAC Name

7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-3a,5a,9-trimethyl-1-(propan-2-yl)-1H,2H,3H,3aH,4H,5H,5aH,6H,7H,8H,10aH,10bH-cyclohepta[e]inden-4-yl 2-methylbutanoate

Traditional Name

7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1H,2H,3H,4H,5H,6H,7H,8H,10aH,10bH-cyclohepta[e]inden-4-yl 2-methylbutanoate

CAS Registry Number

Not Available

SMILES

CCCC(=O)OC1CC2(C)C(C1C(C)C)C1C=C(C)C(O)C(OC(C)=O)C(OC(=O)CCC)C1(C)CC2OC(=O)C(C)CC

InChI Identifier

InChI=1S/C35H56O9/c1-11-14-26(37)42-24-17-35(10)25(43-33(40)20(6)13-3)18-34(9)23(29(35)28(24)19(4)5)16-21(7)30(39)31(41-22(8)36)32(34)44-27(38)15-12-2/h16,19-20,23-25,28-32,39H,11-15,17-18H2,1-10H3

InChI Key

JCOUIOWVKORDDJ-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 sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Tetracarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Secondary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	6.14	ChemAxon
pKa (Strongest Acidic)	13.52	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	125.43 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	164.7 m³·mol⁻¹	ChemAxon
Polarizability	71.12 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

163068232

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)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate (NP0285751)

MOL for NP0285751 (7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate)

3D MOL for NP0285751 (7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate)

3D SDF for NP0285751 (7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate)

3D-SDF for NP0285751 (7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate)

PDB for NP0285751 (7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate)

3D PDB for NP0285751 (7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate)

SMILES for NP0285751 (7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate)

INCHI for NP0285751 (7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate)

Structure for NP0285751 (7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate)

3D Structure for NP0285751 (7-(acetyloxy)-2,6-bis(butanoyloxy)-8-hydroxy-1-isopropyl-3a,5a,9-trimethyl-1h,2h,3h,4h,5h,6h,7h,8h,10ah,10bh-cyclohepta[e]inden-4-yl 2-methylbutanoate)