NP-MRD: Showing NP-Card for 2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate (NP0301679)

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Record Information

Version

2.0

Created at

2022-09-10 14:47:42 UTC

Updated at

2022-09-10 14:47:42 UTC

NP-MRD ID

NP0301679

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate

Description

12,14,15,16-Tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]Heptadec-8-en-2-yl acetate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate is found in Junceella fragilis. 12,14,15,16-Tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]Heptadec-8-en-2-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004181501242D          

 43 45  0  0  0  0            999 V2000
    3.9646    0.0055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4934    0.5463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5711    0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1891   -0.2571    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2042    1.2130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7935    1.7903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7587    2.6146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4552    3.0568    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4205    3.8811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1864    2.6748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8829    3.1170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6141    2.7349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3105    3.1771    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2758    4.0014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9723    4.4436    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5446    4.3835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6488    1.9107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3453    2.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3800    1.5286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0765    1.9708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.5042    2.0310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    7.1460    0.3223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1807   -0.5020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2709   -0.3317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2119    0.9519    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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
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 37 42  1  0  0  0  0
  2 42  1  0  0  0  0
  6 42  1  0  0  0  0
 42 43  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004181501242D          

 43 45  0  0  0  0            999 V2000
    3.9646    0.0055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.6141    2.7349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3453    2.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3800    1.5286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0765    1.9708    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8077    1.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5042    2.0310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8424    0.7645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4147    0.7043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1460    0.3223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1807   -0.5020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9119   -0.8840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4842   -0.9442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7183    0.2621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7530   -0.5622    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0565   -1.0044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0913   -1.8286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3253   -0.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9871    0.6442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2906    0.2020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9523    1.4684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2211    1.8505    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5089    1.0773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9832    0.4415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2709   -0.3317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1697    0.5789    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5247    1.4083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2119    0.9519    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
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 12 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  2  0  0  0  0
 21 23  1  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 29 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 17 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 37 42  1  0  0  0  0
  2 42  1  0  0  0  0
  6 42  1  0  0  0  0
 42 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0301679

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C(=O)OC2C=C(C)CCC(OC(C)=O)C3(C)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(=C)C3C(OC(C)=O)C12O

> <INCHI_IDENTIFIER>
InChI=1S/C30H40O13/c1-13-10-11-21(38-16(4)31)29(9)23(26(41-19(7)34)30(37)15(3)28(36)43-22(30)12-13)14(2)24(39-17(5)32)25(40-18(6)33)27(29)42-20(8)35/h12,15,21-27,37H,2,10-11H2,1,3-9H3

> <INCHI_KEY>
BKPVDGWEAXIPIF-UHFFFAOYSA-N

> <FORMULA>
C30H40O13

> <MOLECULAR_WEIGHT>
608.637

> <EXACT_MASS>
608.246891348

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
59.821197576392876

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate

> <ALOGPS_LOGP>
2.15

> <JCHEM_LOGP>
0.8596590643333326

> <ALOGPS_LOGS>
-3.89

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.349854578134266

> <JCHEM_PKA_STRONGEST_BASIC>
-3.957973607524072

> <JCHEM_POLAR_SURFACE_AREA>
178.03

> <JCHEM_REFRACTIVITY>
143.98170000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.83e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0       7.401   0.010   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.521   1.020   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.799   0.885   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.086  -0.480   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       4.114   2.264   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.214   3.342   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.150   4.881   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.450   5.706   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.385   7.245   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.815   4.993   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.115   5.818   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.480   5.105   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.780   5.931   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.715   7.469   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      13.015   8.295   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      10.350   8.182   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.544   3.567   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      11.845   4.392   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.909   2.853   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      13.209   3.679   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      14.574   2.966   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      15.874   3.791   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      14.639   1.427   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.974   1.315   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      13.339   0.602   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      13.404  -0.937   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      14.769  -1.650   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      12.104  -1.763   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.674   0.489   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      10.739  -1.049   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       9.439  -1.875   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       9.504  -3.413   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       8.074  -1.162   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.309   1.202   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.009   0.377   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.244   2.741   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.879   3.454   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       8.417   2.011   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       7.435   0.824   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       7.972  -0.619   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       5.917   1.081   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.579   2.629   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       7.862   1.777   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   42                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   42                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   12   18   19   36                                             
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25   29                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   24   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   29   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   17   37                                                  
CONECT   37   36   38   42                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42   37    2    6   43                                             
CONECT   43   42                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   90    0
END

View in JSmol

Synonyms

Value	Source
12,14,15,16-Tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0,]heptadec-8-en-2-yl acetic acid	Generator
12,14,15,16-Tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetic acid	Generator

Chemical Formula

C₃₀H₄₀O₁₃

Average Mass

608.6370 Da

Monoisotopic Mass

608.24689 Da

IUPAC Name

2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate

Traditional Name

2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate

CAS Registry Number

Not Available

SMILES

CC1C(=O)OC2C=C(C)CCC(OC(C)=O)C3(C)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(=C)C3C(OC(C)=O)C12O

InChI Identifier

InChI=1S/C30H40O13/c1-13-10-11-21(38-16(4)31)29(9)23(26(41-19(7)34)30(37)15(3)28(36)43-22(30)12-13)14(2)24(39-17(5)32)25(40-18(6)33)27(29)42-20(8)35/h12,15,21-27,37H,2,10-11H2,1,3-9H3

InChI Key

BKPVDGWEAXIPIF-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
Junceella fragilis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Hexacarboxylic acid or derivatives
Briarane diterpenoid
Cyclitol or derivatives
Gamma butyrolactone
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
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
logP	2.15	ALOGPS
logP	0.86	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	12.35	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	178.03 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	143.98 m³·mol⁻¹	ChemAxon
Polarizability	59.82 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	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

73323647

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate (NP0301679)

MOL for NP0301679 (2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate)

3D MOL for NP0301679 (2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate)

3D SDF for NP0301679 (2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate)

3D-SDF for NP0301679 (2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate)

PDB for NP0301679 (2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate)

3D PDB for NP0301679 (2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate)

SMILES for NP0301679 (2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate)

INCHI for NP0301679 (2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate)

Structure for NP0301679 (2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate)

3D Structure for NP0301679 (2,14,15,16-tetrakis(acetyloxy)-3-hydroxy-4,9,13-trimethyl-17-methylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-12-yl acetate)