NP-MRD: Showing NP-Card for 3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate (NP0194191)

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Record Information

Version

2.0

Created at

2022-09-04 11:48:34 UTC

Updated at

2022-09-04 11:48:35 UTC

NP-MRD ID

NP0194191

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate

Description

3,5,9,10A-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1H,2H,3H,3aH,4H,4aH,5H,8H,8aH,9H,10H,10aH-cyclohexa[f]azulen-4-yl butanoate belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. 3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate is found in Euphorbia polycaulis. 3,5,9,10A-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1H,2H,3H,3aH,4H,4aH,5H,8H,8aH,9H,10H,10aH-cyclohexa[f]azulen-4-yl butanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251514452D          

 44 46  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004251514452D          

 44 46  0  0  0  0            999 V2000
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    0.9184   -2.3662    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6329   -1.9537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5713   -1.1310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8507   -0.7292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1021   -1.0760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5725   -0.6011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3211   -0.9479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4985    0.2205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0101    0.0802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4490    0.6850    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8292    0.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1760   -0.5698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6709    0.0903    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3466    0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5275    0.9474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8415    1.5090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9918   -0.6928    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4566   -0.0112    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4043   -1.4073    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0860   -1.8720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0091   -0.8461    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7974   -1.0893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4022   -0.5282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9810   -1.8936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1029   -2.1752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7077   -2.7364    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5241   -3.5407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7358   -3.7839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1310   -3.2227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3426   -3.4659    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1591   -4.2702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7638   -4.8314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3707   -4.5134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3146   -2.4184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5466   -2.7198    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9676   -3.3075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4960   -2.4932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6796   -1.6889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1008   -3.0544    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
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  9 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
  8 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  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
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  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
 36 37  2  0  0  0  0
 36 38  1  0  0  0  0
 34 39  1  0  0  0  0
  7 39  1  0  0  0  0
 30 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 31 42  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0194191

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)OC1C2C(OC(C)=O)C(C)CC2(OC(C)=O)C(=O)C(C)(OC(C)=O)C2C(C=CC(OC(C)=O)C12CO)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C32H44O12/c1-10-11-24(38)42-28-25-26(41-19(6)35)17(4)14-32(25,44-21(8)37)29(39)30(9,43-20(7)36)27-22(16(2)3)12-13-23(40-18(5)34)31(27,28)15-33/h12-13,17,22-23,25-28,33H,2,10-11,14-15H2,1,3-9H3

> <INCHI_KEY>
QJEKFZPZIVYXFD-UHFFFAOYSA-N

> <FORMULA>
C32H44O12

> <MOLECULAR_WEIGHT>
620.692

> <EXACT_MASS>
620.283276857

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
88

> <JCHEM_AVERAGE_POLARIZABILITY>
63.16980449055169

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1H,2H,3H,3aH,4H,4aH,5H,8H,8aH,9H,10H,10aH-cyclohexa[f]azulen-4-yl butanoate

> <ALOGPS_LOGP>
2.71

> <JCHEM_LOGP>
2.211557949333333

> <ALOGPS_LOGS>
-4.32

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.922171340462146

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8328422556818555

> <JCHEM_POLAR_SURFACE_AREA>
168.79999999999998

> <JCHEM_REFRACTIVITY>
153.25879999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.00e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1H,2H,3H,3aH,4H,5H,8H,8aH-cyclohexa[f]azulen-4-yl butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -3.620  -4.417   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.287  -3.647   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.953  -4.417   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.381  -3.647   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.524  -2.401   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       1.714  -4.417   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.048  -3.647   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.933  -2.111   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.588  -1.361   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.191  -2.009   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.069  -1.122   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -2.466  -1.769   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.931   0.412   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.886   0.150   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.838   1.279   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.415   0.334   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.062  -1.064   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.986   0.168   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.380   1.585   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.851   1.768   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.304   2.817   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.585  -1.293   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.452  -0.021   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.355  -2.627   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.627  -3.494   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.484  -1.579   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       8.955  -2.033   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.084  -0.986   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       9.298  -3.535   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.792  -4.060   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.921  -5.108   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.578  -6.609   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.107  -7.063   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       3.978  -6.016   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       2.506  -6.470   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       2.164  -7.971   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       3.292  -9.019   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       0.692  -8.425   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.321  -4.514   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.887  -5.077   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       1.806  -6.174   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       8.393  -4.654   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       8.735  -3.153   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       9.521  -5.701   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   39                                                  
CONECT    8    7    9   17                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16    8   18   22                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26   30                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   24   31   39                                                  
CONECT   31   30   32   42                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   34    7   30   40                                             
CONECT   40   39   41                                                       
CONECT   41   40                                                            
CONECT   42   31   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
3,5,9,10a-Tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1H,2H,3H,3ah,4H,4ah,5H,8H,8ah,9H,10H,10ah-cyclohexa[F]azulen-4-yl butanoic acid	Generator

Chemical Formula

C₃₂H₄₄O₁₂

Average Mass

620.6920 Da

Monoisotopic Mass

620.28328 Da

IUPAC Name

3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1H,2H,3H,3aH,4H,4aH,5H,8H,8aH,9H,10H,10aH-cyclohexa[f]azulen-4-yl butanoate

Traditional Name

3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1H,2H,3H,3aH,4H,5H,8H,8aH-cyclohexa[f]azulen-4-yl butanoate

CAS Registry Number

Not Available

SMILES

CCCC(=O)OC1C2C(OC(C)=O)C(C)CC2(OC(C)=O)C(=O)C(C)(OC(C)=O)C2C(C=CC(OC(C)=O)C12CO)C(C)=C

InChI Identifier

InChI=1S/C32H44O12/c1-10-11-24(38)42-28-25-26(41-19(6)35)17(4)14-32(25,44-21(8)37)29(39)30(9,43-20(7)36)27-22(16(2)3)12-13-23(40-18(5)34)31(27,28)15-33/h12-13,17,22-23,25-28,33H,2,10-11,14-15H2,1,3-9H3

InChI Key

QJEKFZPZIVYXFD-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

Species Name	Source	Reference
Euphorbia polycaulis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Alpha-acyloxy ketone
Fatty acid ester
Fatty acyl
Ketone
Carboxylic acid ester
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
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	2.71	ALOGPS
logP	2.21	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	14.92	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	168.8 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	153.26 m³·mol⁻¹	ChemAxon
Polarizability	63.17 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate (NP0194191)

MOL for NP0194191 (3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate)

3D MOL for NP0194191 (3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate)

3D SDF for NP0194191 (3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate)

3D-SDF for NP0194191 (3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate)

PDB for NP0194191 (3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate)

3D PDB for NP0194191 (3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate)

SMILES for NP0194191 (3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate)

INCHI for NP0194191 (3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate)

Structure for NP0194191 (3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate)

3D Structure for NP0194191 (3,5,9,10a-tetrakis(acetyloxy)-4a-(hydroxymethyl)-2,9-dimethyl-10-oxo-8-(prop-1-en-2-yl)-1h,2h,3h,3ah,4h,5h,8h,8ah-cyclohexa[f]azulen-4-yl butanoate)