NP-MRD: Showing NP-Card for 3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate (NP0142947)

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Record Information

Version

2.0

Created at

2022-09-01 21:36:07 UTC

Updated at

2022-09-01 21:36:08 UTC

NP-MRD ID

NP0142947

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate

Description

15-[2-(Acetyloxy)-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]Octadec-12-en-3-yl acetate belongs to the class of organic compounds known as limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17. 15-[2-(Acetyloxy)-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]Octadec-12-en-3-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251514092D          

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M  END

     RDKit          3D

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M  END


  Mrv1533004251514092D          

 42 46  0  0  0  0            999 V2000
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   -1.5728   -1.3607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3024   -2.1402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4776   -2.1239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2382   -1.3344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5413   -1.0640    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6968   -0.2538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4763    0.0165    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0730    0.2860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9151   -0.8627    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0204   -2.7816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2190   -3.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4578   -4.0428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1156   -3.5448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8452   -2.7654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4949   -2.0185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3851   -2.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1953   -2.2971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4656   -3.0765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2758   -3.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9480   -2.4751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7166   -2.5348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5367   -2.4446    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1185   -3.0296    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8979   -2.7592    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0239   -3.8492    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3241   -4.2862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9059   -4.8711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8833   -4.9835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5462   -4.0116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0063   -4.6354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1961   -4.4798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6563   -5.1037    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9258   -3.7004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3859   -4.3243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2796   -1.8350    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6671   -1.1067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2301   -0.4070    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4916   -1.0781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7539   -1.4459    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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
  7 12  1  0  0  0  0
  4 12  1  0  0  0  0
  6 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 13 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
 22 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
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 22 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 16 36  1  0  0  0  0
 21 36  1  0  0  0  0
 36 37  1  0  0  0  0
 24 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
  2 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0142947

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1OC(CC1C1CC=C2C1(C)CCC1C3(C)C(CC(O)C21C)C(C)(C)OC(=O)CC3OC(C)=O)C=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C34H50O8/c1-18(2)14-21-15-22(30(41-21)40-20(4)36)23-10-11-24-32(23,7)13-12-25-33(24,8)27(37)16-26-31(5,6)42-29(38)17-28(34(25,26)9)39-19(3)35/h11,14,21-23,25-28,30,37H,10,12-13,15-17H2,1-9H3

> <INCHI_KEY>
KARYHQFKNHLQCX-UHFFFAOYSA-N

> <FORMULA>
C34H50O8

> <MOLECULAR_WEIGHT>
586.766

> <EXACT_MASS>
586.35056857

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
65.7359183493927

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate

> <ALOGPS_LOGP>
5.41

> <JCHEM_LOGP>
4.210586355666664

> <ALOGPS_LOGS>
-5.72

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.623872398440326

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9633182129222

> <JCHEM_POLAR_SURFACE_AREA>
108.36000000000001

> <JCHEM_REFRACTIVITY>
157.27840000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.12e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate

> <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      -5.184  -4.646   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.534  -3.146   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.410  -2.093   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.936  -2.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.431  -3.995   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.892  -3.965   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.445  -2.491   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.010  -1.986   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       1.301  -0.474   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.756   0.031   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.136   0.534   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.708  -1.610   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.038  -5.192   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.409  -6.666   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.855  -7.547   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.082  -6.617   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.578  -5.162   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.924  -3.768   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.585  -3.998   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.098  -4.288   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.602  -5.743   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.115  -6.033   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.503  -4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.938  -4.732   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.468  -4.563   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.554  -5.655   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      11.009  -5.151   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       9.378  -7.185   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       8.072  -8.001   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.158  -9.093   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.249  -9.303   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.620  -7.488   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.612  -8.653   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.099  -8.362   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.092  -9.527   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.595  -6.907   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.587  -8.072   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       6.122  -3.425   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       6.845  -2.066   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       6.029  -0.760   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       8.384  -2.012   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -7.007  -2.699   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   42                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   13                                                  
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7    4                                                       
CONECT   13    6   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   36                                                  
CONECT   17   16   13   18   19                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   36                                                  
CONECT   22   21   23   24   32                                             
CONECT   23   22                                                            
CONECT   24   22   25   38                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   31   32                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   29   22   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   16   21   37                                             
CONECT   37   36                                                            
CONECT   38   24   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
CONECT   42    2                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

View in JSmol

Synonyms

Value	Source
15-[2-(Acetyloxy)-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0,.0,]octadec-12-en-3-yl acetic acid	Generator
15-[2-(Acetyloxy)-5-(2-methylprop-1-en-1-yl)oxolan-3-yl]-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-3-yl acetic acid	Generator

Chemical Formula

C₃₄H₅₀O₈

Average Mass

586.7660 Da

Monoisotopic Mass

586.35057 Da

IUPAC Name

3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate

Traditional Name

3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1OC(CC1C1CC=C2C1(C)CCC1C3(C)C(CC(O)C21C)C(C)(C)OC(=O)CC3OC(C)=O)C=C(C)C

InChI Identifier

InChI=1S/C34H50O8/c1-18(2)14-21-15-22(30(41-21)40-20(4)36)23-10-11-24-32(23,7)13-12-25-33(24,8)27(37)16-26-31(5,6)42-29(38)17-28(34(25,26)9)39-19(3)35/h11,14,21-23,25-28,30,37H,10,12-13,15-17H2,1-9H3

InChI Key

KARYHQFKNHLQCX-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 limonoids. These are highly oxygenated, modified terpenoids with a prototypical structure either containing or derived from a precursor with a 4,4,8-trimethyl-17-furanylsteroid skeleton. All naturally occurring citrus limonoids contain a furan ring attached to the D-ring, at C-17, as well as oxygen containing functional groups at C-3, C-4, C-7, C-16 and C-17.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Limonoids

Alternative Parents

Substituents

Limonoid skeleton
Tricarboxylic acid or derivatives
Caprolactone
Oxepane
Cyclic alcohol
Tetrahydrofuran
Carboxylic acid ester
Lactone
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Organic oxide
Alcohol
Carbonyl group
Hydrocarbon derivative
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	5.41	ALOGPS
logP	4.21	ChemAxon
logS	-5.7	ALOGPS
pKa (Strongest Acidic)	14.62	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	108.36 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	157.28 m³·mol⁻¹	ChemAxon
Polarizability	65.74 Å³	ChemAxon
Number of Rings	5	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

Not Available

PDB ID

Not Available

ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for 3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate (NP0142947)

MOL for NP0142947 (3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate)

3D MOL for NP0142947 (3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate)

3D SDF for NP0142947 (3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate)

3D-SDF for NP0142947 (3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate)

PDB for NP0142947 (3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate)

3D PDB for NP0142947 (3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate)

SMILES for NP0142947 (3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate)

INCHI for NP0142947 (3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate)

Structure for NP0142947 (3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate)

3D Structure for NP0142947 (3-[3-(acetyloxy)-10-hydroxy-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadec-12-en-15-yl]-5-(2-methylprop-1-en-1-yl)oxolan-2-yl acetate)