NP-MRD: Showing NP-Card for 2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate (NP0287341)

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Record Information

Version

2.0

Created at

2022-09-09 16:21:58 UTC

Updated at

2022-09-09 16:21:58 UTC

NP-MRD ID

NP0287341

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate

Description

2,7-Bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]Hexadec-12-en-8-yl pyridine-3-carboxylate belongs to the class of organic compounds known as pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups. Based on a literature review very few articles have been published on 2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]Hexadec-12-en-8-yl pyridine-3-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092218212D          

 53 58  0  0  0  0            999 V2000
    1.4394   -2.6037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7025   -2.1773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1502   -2.9078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9899   -1.2560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1025   -1.2502    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3574   -0.6797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2759    0.1682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0206    1.0120    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7684    1.4143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4702    0.9805    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932    2.2389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5197    2.6298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
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  7 17  1  0  0  0  0
 17 18  1  0  0  0  0
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 23 33  1  0  0  0  0
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 33 47  1  0  0  0  0
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 21 53  1  0  0  0  0
  4 53  1  0  0  0  0
 17 53  1  0  0  0  0
M  END

     RDKit          3D

 98103  0  0  0  0  0  0  0  0999 V2000
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  3 56  1  0
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 38 88  1  6
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 45 91  1  0
 47 92  1  0
M  END


  Mrv1652309092218212D          

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    2.9953   -2.5361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7933   -3.8016    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3674   -3.8941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4208   -4.7174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7345   -5.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -4.8099    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9414   -3.9866    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6277   -3.5287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7060   -1.1030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0157   -1.9625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8446   -2.0495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3294   -1.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1803   -2.8031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5208   -1.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8955   -0.4972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.2295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3122    0.0863    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6651    0.8823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4310    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1348    0.8685    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4519    2.1237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1765    2.5180    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5771   -0.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9097    0.1969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9571    1.0731    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5228    1.7979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6979    1.7846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9237    2.5190    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4175   -0.6913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  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
 11 12  2  0  0  0  0
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 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
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 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
 23 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  0  0  0
 33 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 41 47  1  0  0  0  0
 33 47  1  0  0  0  0
 47 48  1  0  0  0  0
 17 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  2  0  0  0  0
 21 53  1  0  0  0  0
  4 53  1  0  0  0  0
 17 53  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287341

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(=O)OC1C(C)CC2(OC(C)=O)C1C(OC(C)=O)C13C(O)OC(C)(C1C(C=CC3OC(=O)C1=CC=CC=C1)C(C)=C)C2OC(=O)C1=CC=CN=C1

> <INCHI_IDENTIFIER>
InChI=1S/C40H45NO12/c1-8-29(44)50-31-22(4)19-39(52-24(6)43)30(31)33(48-23(5)42)40-28(49-34(45)25-13-10-9-11-14-25)17-16-27(21(2)3)32(40)38(7,53-37(40)47)36(39)51-35(46)26-15-12-18-41-20-26/h9-18,20,22,27-28,30-33,36-37,47H,2,8,19H2,1,3-7H3

> <INCHI_KEY>
BEUFBQVEVMOJCV-UHFFFAOYSA-N

> <FORMULA>
C40H45NO12

> <MOLECULAR_WEIGHT>
731.795

> <EXACT_MASS>
731.294175893

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
98

> <JCHEM_AVERAGE_POLARIZABILITY>
74.31329784886631

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0^{1,10}.0^{3,7}]hexadec-12-en-8-yl pyridine-3-carboxylate

> <JCHEM_LOGP>
4.535590754999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.758044428480869

> <JCHEM_PKA_STRONGEST_BASIC>
3.2388747075080926

> <JCHEM_POLAR_SURFACE_AREA>
173.84999999999997

> <JCHEM_REFRACTIVITY>
185.97820000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0^{1,10}.0^{3,7}]hexadec-12-en-8-yl pyridine-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       2.687  -4.860   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.311  -4.064   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.280  -5.428   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.848  -2.345   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.191  -2.334   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.667  -1.269   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.515   0.314   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -0.038   1.889   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.434   2.640   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -2.744   1.830   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.481   4.179   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.837   4.909   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.883   6.448   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.573   7.258   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.217   6.528   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.171   4.989   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.044   0.127   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.138  -1.119   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.418  -0.203   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       1.379  -2.640   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.625  -3.545   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.881  -5.352   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.146  -3.305   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.591  -4.734   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.700  -6.414   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       7.081  -7.096   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.419  -7.269   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.519  -8.806   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.238  -9.660   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.857  -8.978   0.000  0.00  0.00           C+0
HETATM   31  N   UNK     0       1.757  -7.442   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0       3.038  -6.587   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.051  -2.059   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       5.629  -3.663   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       7.177  -3.826   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.082  -2.580   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       7.803  -5.232   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       6.572  -2.300   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.272  -0.928   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.788  -0.428   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.183   0.161   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       6.842   1.647   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       8.271   2.425   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       9.585   1.621   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       8.310   3.964   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       9.663   4.700   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       4.811  -0.538   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       3.565   0.368   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       3.653   2.003   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       2.843   3.356   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       1.303   3.331   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0       3.591   4.702   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0       2.646  -1.290   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   53                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   17                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17    7   18   48   53                                             
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23   53                                             
CONECT   22   21                                                            
CONECT   23   21   24   33                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   27                                                       
CONECT   33   23   34   38   47                                             
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   33   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   47                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46                                                       
CONECT   46   45                                                            
CONECT   47   41   33   48                                                  
CONECT   48   47   17   49                                                  
CONECT   49   48   50                                                       
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50                                                            
CONECT   53   21    4   17                                                  
MASTER        0    0    0    0    0    0    0    0   53    0  116    0
END

View in JSmol

Synonyms

Value	Source
2,7-Bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0,.0,]hexadec-12-en-8-yl pyridine-3-carboxylic acid	Generator

Chemical Formula

C₄₀H₄₅NO₁₂

Average Mass

731.7950 Da

Monoisotopic Mass

731.29418 Da

IUPAC Name

2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0^{1,10}.0^{3,7}]hexadec-12-en-8-yl pyridine-3-carboxylate

Traditional Name

2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0^{1,10}.0^{3,7}]hexadec-12-en-8-yl pyridine-3-carboxylate

CAS Registry Number

Not Available

SMILES

CCC(=O)OC1C(C)CC2(OC(C)=O)C1C(OC(C)=O)C13C(O)OC(C)(C1C(C=CC3OC(=O)C1=CC=CC=C1)C(C)=C)C2OC(=O)C1=CC=CN=C1

InChI Identifier

InChI=1S/C40H45NO12/c1-8-29(44)50-31-22(4)19-39(52-24(6)43)30(31)33(48-23(5)42)40-28(49-34(45)25-13-10-9-11-14-25)17-16-27(21(2)3)32(40)38(7,53-37(40)47)36(39)51-35(46)26-15-12-18-41-20-26/h9-18,20,22,27-28,30-33,36-37,47H,2,8,19H2,1,3-7H3

InChI Key

BEUFBQVEVMOJCV-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 pentacarboxylic acids and derivatives. These are carboxylic acids containing exactly five carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Pentacarboxylic acids and derivatives

Direct Parent

Pentacarboxylic acids and derivatives

Alternative Parents

Substituents

Pentacarboxylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Pyridine carboxylic acid
Pyridine carboxylic acid or derivatives
Benzoyl
Monocyclic benzene moiety
Pyridine
Benzenoid
Heteroaromatic compound
Tetrahydrofuran
Carboxylic acid ester
Hemiacetal
Oxacycle
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Carbonyl group
Organic oxide
Organopnictogen compound
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	4.54	ChemAxon
pKa (Strongest Acidic)	11.76	ChemAxon
pKa (Strongest Basic)	3.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	173.85 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	185.98 m³·mol⁻¹	ChemAxon
Polarizability	74.31 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

85211820

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate (NP0287341)

MOL for NP0287341 (2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate)

3D MOL for NP0287341 (2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate)

3D SDF for NP0287341 (2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate)

3D-SDF for NP0287341 (2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate)

PDB for NP0287341 (2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate)

3D PDB for NP0287341 (2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate)

SMILES for NP0287341 (2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate)

INCHI for NP0287341 (2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate)

Structure for NP0287341 (2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate)

3D Structure for NP0287341 (2,7-bis(acetyloxy)-14-(benzoyloxy)-15-hydroxy-5,9-dimethyl-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-8-yl pyridine-3-carboxylate)