NP-MRD: Showing NP-Card for 18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate (NP0286403)

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Record Information

Version

2.0

Created at

2022-09-09 14:57:35 UTC

Updated at

2022-09-09 14:57:35 UTC

NP-MRD ID

NP0286403

Secondary Accession Numbers

None

Natural Product Identification

Common Name

18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate

Description

18-(Acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]Henicosan-20-yl 2-methylbut-2-enoate 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. 18-(Acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]Henicosan-20-yl 2-methylbut-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171517372D          

 43 49  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004171517372D          

 43 49  0  0  0  0            999 V2000
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    0.8351   -0.0449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0651    0.2513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5764   -0.2674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4480   -1.0823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3464    0.0288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4767    0.4738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7419    0.8489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5205    1.2976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3175    1.5105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7663    0.8183    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5811    0.6886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1007    1.3294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8761   -0.0818    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9199    0.7420    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3565   -0.7226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6515   -1.4930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4663   -1.6227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9859   -0.9819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2810   -1.7524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8007   -1.1116    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3204   -0.4709    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0253    0.2996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5450    0.9403    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2106    0.4293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3958    0.5589    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6909   -0.2115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0958   -1.8820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6459   -2.5736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1646   -3.2151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9350   -2.9201    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8925   -2.0962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3751   -0.6374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6163   -1.4264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2466    0.1775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  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  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 10 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
 18 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
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 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
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 22 35  1  0  0  0  0
 27 35  1  0  0  0  0
 33 35  1  0  0  0  0
 29 36  1  0  0  0  0
 36 37  2  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
 36 40  1  0  0  0  0
 24 41  1  0  0  0  0
  8 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  1  0  0  0  0
 15 43  1  0  0  0  0
 19 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0286403

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OC1CC(OC(C)=O)C2(C)COC3C2C1(C)C1CCC2(C)C(OC(=O)C4OC24C1(C)C3O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C33H42O10/c1-8-16(2)27(36)41-21-13-20(40-17(3)34)29(4)15-39-22-23(29)31(21,6)19-9-11-30(5)25(18-10-12-38-14-18)42-28(37)26-33(30,43-26)32(19,7)24(22)35/h8,10,12,14,19-26,35H,9,11,13,15H2,1-7H3

> <INCHI_KEY>
AKMYXCRNLALNAA-UHFFFAOYSA-N

> <FORMULA>
C33H42O10

> <MOLECULAR_WEIGHT>
598.689

> <EXACT_MASS>
598.277797552

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
62.720630607112625

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate

> <ALOGPS_LOGP>
4.28

> <JCHEM_LOGP>
3.531947818

> <ALOGPS_LOGS>
-4.27

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.649013658761298

> <JCHEM_PKA_STRONGEST_BASIC>
-2.85125308264595

> <JCHEM_POLAR_SURFACE_AREA>
134.03000000000003

> <JCHEM_REFRACTIVITY>
149.57279999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.22e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       1.560  -8.658   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.320  -7.137   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.518  -6.169   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.955  -6.722   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.278  -4.648   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.841  -4.095   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       3.476  -3.679   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.236  -2.158   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.799  -1.605   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.559  -0.084   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       0.122   0.469   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.076  -0.499   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.836  -2.020   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.513   0.054   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.756   0.884   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.385   1.585   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.838   2.422   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.326   2.820   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.164   1.527   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.685   1.285   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.655   2.481   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       7.235  -0.153   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.317   1.385   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.265  -1.349   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.816  -2.787   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.337  -3.029   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.307  -1.833   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.858  -3.271   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.828  -2.075   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      11.798  -0.879   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      11.247   0.559   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      12.217   1.755   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       9.726   0.801   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       8.206   1.043   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.756  -0.395   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      11.379  -3.513   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      10.539  -4.804   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      11.507  -6.002   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      12.945  -5.451   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      12.866  -3.913   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.433  -1.190   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.884  -2.663   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.194   0.331   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   41                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   10   16   17   43                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   43                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24   35                                             
CONECT   23   22                                                            
CONECT   24   22   25   41                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   35                                             
CONECT   28   27                                                            
CONECT   29   27   30   36                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33   35                                                       
CONECT   35   34   22   27   33                                             
CONECT   36   29   37   40                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   36                                                       
CONECT   41   24    8   42   43                                             
CONECT   42   41                                                            
CONECT   43   41   15   19                                                  
MASTER        0    0    0    0    0    0    0    0   43    0   98    0
END

View in JSmol

Synonyms

Value	Source
18-(Acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0,.0,.0,.0,]henicosan-20-yl 2-methylbut-2-enoic acid	Generator
18-(Acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoic acid	Generator

Chemical Formula

C₃₃H₄₂O₁₀

Average Mass

598.6890 Da

Monoisotopic Mass

598.27780 Da

IUPAC Name

18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate

Traditional Name

18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OC1CC(OC(C)=O)C2(C)COC3C2C1(C)C1CCC2(C)C(OC(=O)C4OC24C1(C)C3O)C1=COC=C1

InChI Identifier

InChI=1S/C33H42O10/c1-8-16(2)27(36)41-21-13-20(40-17(3)34)29(4)15-39-22-23(29)31(21,6)19-9-11-30(5)25(18-10-12-38-14-18)42-28(37)26-33(30,43-26)32(19,7)24(22)35/h8,10,12,14,19-26,35H,9,11,13,15H2,1-7H3

InChI Key

AKMYXCRNLALNAA-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
Naphthopyran
Naphthofuran
Naphthalene
Tricarboxylic acid or derivatives
Delta valerolactone
Dioxepane
Fatty acid ester
Delta_valerolactone
1,4-dioxepane
Fatty acyl
Oxane
Pyran
Tetrahydrofuran
Heteroaromatic compound
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Furan
Secondary alcohol
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Dialkyl ether
Organoheterocyclic compound
Oxirane
Ether
Organic oxide
Organooxygen compound
Carbonyl group
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	4.28	ALOGPS
logP	3.53	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	13.65	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	134.03 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	149.57 m³·mol⁻¹	ChemAxon
Polarizability	62.72 Å³	ChemAxon
Number of Rings	7	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 18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate (NP0286403)

MOL for NP0286403 (18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate)

3D MOL for NP0286403 (18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate)

3D SDF for NP0286403 (18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate)

3D-SDF for NP0286403 (18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate)

PDB for NP0286403 (18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate)

3D PDB for NP0286403 (18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate)

SMILES for NP0286403 (18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate)

INCHI for NP0286403 (18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate)

Structure for NP0286403 (18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate)

3D Structure for NP0286403 (18-(acetyloxy)-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.0²,¹².0⁵,¹¹.0⁹,¹¹.0¹⁷,²¹]henicosan-20-yl 2-methylbut-2-enoate)