NP-MRD: Showing NP-Card for 5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate (NP0315752)

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Record Information

Version

2.0

Created at

2022-09-11 14:32:24 UTC

Updated at

2022-09-11 14:32:24 UTC

NP-MRD ID

NP0315752

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate

Description

5-(Acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-4-yl pyridine-3-carboxylate belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene). Based on a literature review very few articles have been published on 5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]Dodecan-4-yl pyridine-3-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112216322D          

 47 52  0  0  0  0            999 V2000
    5.6612   -2.5857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1933   -1.8590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.3750   -1.4994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5838   -0.9369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0331   -0.2371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7033    0.3329    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4614    0.7949    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2503    1.6361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2535    0.3933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7882    1.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5996    0.8728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.6599    0.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 42 47  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309112216322D          

 47 52  0  0  0  0            999 V2000
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    5.2503    1.6361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2535    0.3933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7882    1.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5996    0.8728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8764    0.0956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3418   -0.5327    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.5303   -0.3838    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6599    0.5054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8351    0.5561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7693    1.4202    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3349   -0.1234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6531    0.4578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8934    0.0350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4630    0.8017    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0161    0.0067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0588   -0.8122    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4269   -1.5948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2845   -1.6626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5878   -2.5405    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0707   -3.3554    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2633   -3.6422    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3855   -4.0885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2105   -4.0863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6249   -4.7996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2143   -5.5152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3893   -5.5174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9749   -4.8040    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7420   -0.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3960   -1.5145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7368   -0.5133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9762   -1.2665    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6215   -2.1036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9552   -2.7994    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8653   -2.4497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6640   -3.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1295   -3.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7217   -2.9011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5204   -2.1010    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2731   -1.8753    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
  2  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  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 10 15  1  0  0  0  0
  6 16  1  0  0  0  0
 16 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
 21 23  1  0  0  0  0
 21 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
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  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  2  0  0  0  0
 30 35  1  0  0  0  0
 26 36  1  0  0  0  0
  5 36  1  0  0  0  0
 19 36  1  0  0  0  0
 36 37  1  0  0  0  0
 24 38  1  0  0  0  0
 19 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  2  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 42 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0315752

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(OC(=O)C2=CC=CN=C2)C(OC(C)=O)C2(C)C(CC3C(OC(=O)C4=CC=CN=C4)C12OC3(C)C)OC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C36H38N2O9/c1-21-17-27(44-32(41)24-13-9-15-37-19-24)30(43-22(2)39)35(5)28(45-31(40)23-11-7-6-8-12-23)18-26-29(36(21,35)47-34(26,3)4)46-33(42)25-14-10-16-38-20-25/h6-16,19-21,26-30H,17-18H2,1-5H3

> <INCHI_KEY>
FVMMOSQBOWPRQW-UHFFFAOYSA-N

> <FORMULA>
C36H38N2O9

> <MOLECULAR_WEIGHT>
642.705

> <EXACT_MASS>
642.257730812

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
66.01757724061879

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl pyridine-3-carboxylate

> <JCHEM_LOGP>
4.881538747666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.5410383220687005

> <JCHEM_POLAR_SURFACE_AREA>
140.21000000000004

> <JCHEM_REFRACTIVITY>
166.4839

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl pyridine-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      10.568  -4.827   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.694  -3.470   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.953  -2.588   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.167  -2.799   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.690  -1.749   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.528  -0.443   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.780   0.621   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.195   1.484   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       9.800   3.054   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.673   0.734   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.671   1.907   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.186   1.629   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.703   0.179   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      13.705  -0.994   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      12.190  -0.717   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.832   0.943   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.292   1.038   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.169   2.651   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.358  -0.230   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       3.086   0.855   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.668   0.065   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.864   1.496   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.030   0.013   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.976  -1.516   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.664  -2.977   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.264  -3.104   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.831  -4.742   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       3.865  -6.263   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       2.358  -6.799   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.453  -7.632   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.993  -7.628   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.767  -8.959   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.000 -10.295   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.460 -10.299   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.687  -8.968   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.118  -1.701   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.339  -2.827   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.242  -0.958   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       3.689  -2.364   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       3.027  -3.927   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       3.650  -5.225   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       1.615  -4.573   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.240  -6.066   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -0.242  -6.488   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -1.347  -5.415   0.000  0.00  0.00           C+0
HETATM   46  N   UNK     0      -0.971  -3.922   0.000  0.00  0.00           N+0
HETATM   47  C   UNK     0       0.510  -3.501   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   36                                                  
CONECT    6    5    7   16                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16    6   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   36   38                                             
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21   25   38                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   36                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   35                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   30                                                       
CONECT   36   26    5   19   37                                             
CONECT   37   36                                                            
CONECT   38   24   19   39                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   47                                                  
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   42                                                       
MASTER        0    0    0    0    0    0    0    0   47    0  104    0
END

View in JSmol

Synonyms

Value	Source
5-(Acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0,]dodecan-4-yl pyridine-3-carboxylic acid	Generator

Chemical Formula

C₃₆H₃₈N₂O₉

Average Mass

642.7050 Da

Monoisotopic Mass

642.25773 Da

IUPAC Name

5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl pyridine-3-carboxylate

Traditional Name

5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0^{1,6}]dodecan-4-yl pyridine-3-carboxylate

CAS Registry Number

Not Available

SMILES

CC1CC(OC(=O)C2=CC=CN=C2)C(OC(C)=O)C2(C)C(CC3C(OC(=O)C4=CC=CN=C4)C12OC3(C)C)OC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C36H38N2O9/c1-21-17-27(44-32(41)24-13-9-15-37-19-24)30(43-22(2)39)35(5)28(45-31(40)23-11-7-6-8-12-23)18-26-29(36(21,35)47-34(26,3)4)46-33(42)25-14-10-16-38-20-25/h6-16,19-21,26-30H,17-18H2,1-5H3

InChI Key

FVMMOSQBOWPRQW-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 agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Agarofurans

Alternative Parents

Substituents

Agarofuran
Tetracarboxylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Pyridine carboxylic acid
Pyridine carboxylic acid or derivatives
Benzoyl
Oxepane
Monocyclic benzene moiety
Benzenoid
Pyridine
Heteroaromatic compound
Tetrahydrofuran
Carboxylic acid ester
Carboxylic acid derivative
Oxacycle
Dialkyl ether
Ether
Azacycle
Organoheterocyclic compound
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Organic oxide
Hydrocarbon derivative
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	4.88	ChemAxon
pKa (Strongest Basic)	3.54	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	140.21 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	166.48 m³·mol⁻¹	ChemAxon
Polarizability	66.02 Å³	ChemAxon
Number of Rings	6	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

78192778

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate (NP0315752)

MOL for NP0315752 (5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate)

3D MOL for NP0315752 (5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate)

3D SDF for NP0315752 (5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate)

3D-SDF for NP0315752 (5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate)

PDB for NP0315752 (5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate)

3D PDB for NP0315752 (5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate)

SMILES for NP0315752 (5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate)

INCHI for NP0315752 (5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate)

Structure for NP0315752 (5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate)

3D Structure for NP0315752 (5-(acetyloxy)-7-(benzoyloxy)-2,6,10,10-tetramethyl-12-(pyridine-3-carbonyloxy)-11-oxatricyclo[7.2.1.0¹,⁶]dodecan-4-yl pyridine-3-carboxylate)