NP-MRD: Showing NP-Card for 7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate (NP0169636)

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Record Information

Version

2.0

Created at

2022-09-03 05:37:57 UTC

Updated at

2022-09-03 05:37:57 UTC

NP-MRD ID

NP0169636

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

7-(Acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]Hexadec-12-en-14-yl pyridine-3-carboxylate belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups. 7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate is found in Euphorbia myrsinites. 7-(Acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]Hexadec-12-en-14-yl pyridine-3-carboxylate is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241503482D          

 46 50  0  0  0  0            999 V2000
    3.5636   -3.0264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5382   -2.2018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7926   -1.8014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4700   -0.9955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2950   -0.9870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0304   -0.2519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8797    0.6222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5500    1.1032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2829    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9020    0.1172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7422    0.0430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
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 29 43  1  0  0  0  0
 42 44  1  0  0  0  0
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 44 46  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004241503482D          

 46 50  0  0  0  0            999 V2000
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    3.5382   -2.2018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7926   -1.8014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4700   -0.9955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2950   -0.9870    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0304   -0.2519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8797    0.6222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5500    1.1032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2829    0.7243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9020    0.1172    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7422    0.0430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2159    0.7184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0902   -0.7050    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9120   -0.7776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8697    1.3042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7216    1.3819    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4994    2.0415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6839    1.9172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1140    2.7846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8801    3.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8618    4.0746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6035    2.8532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2029    2.5875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1393    3.4947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4568    2.6266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1366    3.4479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6505    2.3351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5847    1.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0657    0.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2462    0.6608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0654   -0.1697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9329   -0.1526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3594   -0.8588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3312    0.5699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1561    0.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5544    1.3087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1279    2.0149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3030    1.9986    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9047    1.2761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2460    1.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0813    2.0802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9008    2.1754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3930    1.5133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7272    3.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5112    3.7948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1588    3.8644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  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  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  9 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
  8 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 18 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
  7 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 34 39  1  0  0  0  0
 30 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 25 43  1  0  0  0  0
 29 43  1  0  0  0  0
 42 44  1  0  0  0  0
 44 45  2  0  0  0  0
 44 46  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0169636

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)OC1C2C(OC(=O)CC)C(C)CC2(OC(C)=O)C(=O)C2(C)OCC11C2C(C=CC1OC(=O)C1=CC=CN=C1)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C35H43NO10/c1-8-11-26(39)45-30-27-28(44-25(38)9-2)20(5)16-35(27,46-21(6)37)32(41)33(7)29-23(19(3)4)13-14-24(34(29,30)18-42-33)43-31(40)22-12-10-15-36-17-22/h10,12-15,17,20,23-24,27-30H,3,8-9,11,16,18H2,1-2,4-7H3

> <INCHI_KEY>
MVADZRSXUXTRLD-UHFFFAOYSA-N

> <FORMULA>
C35H43NO10

> <MOLECULAR_WEIGHT>
637.726

> <EXACT_MASS>
637.288696589

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
66.02089146012266

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate

> <ALOGPS_LOGP>
3.74

> <JCHEM_LOGP>
4.469173969666667

> <ALOGPS_LOGS>
-5.05

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
3.2386483835215167

> <JCHEM_POLAR_SURFACE_AREA>
144.39

> <JCHEM_REFRACTIVITY>
163.73769999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.64e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       6.652  -5.649   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.605  -4.110   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.213  -3.363   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.611  -1.858   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.151  -1.842   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       3.790  -0.470   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       3.509   1.161   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.760   2.059   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.128   1.352   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.284   0.219   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.852   0.080   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.736   1.341   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       9.502  -1.316   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.036  -1.451   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.223   2.435   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.814   2.579   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.532   3.811   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.010   3.579   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.813   5.198   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       7.243   6.066   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.209   7.606   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.593   5.326   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.112   4.830   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       3.993   6.523   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       2.719   4.903   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.122   6.436   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       1.214   4.359   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.091   2.662   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.989   1.411   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.460   1.233   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -0.122  -0.317   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -1.741  -0.285   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -2.538  -1.603   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -2.485   1.064   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -4.025   1.094   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -4.768   2.443   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -3.972   3.761   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0      -2.432   3.731   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0      -1.689   2.382   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -0.459   2.469   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       0.152   3.883   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       1.681   4.061   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.600   2.825   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.357   5.870   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.821   7.084   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       0.296   7.213   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   29                                                  
CONECT    8    7    9   18                                                  
CONECT    9    8   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13                                                            
CONECT   15    9   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17    8   19   23                                             
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27   43                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28    7   30   43                                             
CONECT   30   29   31   40                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   39                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   34                                                       
CONECT   40   30   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42   25   29                                                  
CONECT   44   42   45   46                                                  
CONECT   45   44                                                            
CONECT   46   44                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  100    0
END

View in JSmol

Synonyms

Value	Source
7-(Acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0,.0,]hexadec-12-en-14-yl pyridine-3-carboxylic acid	Generator
7-(Acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylic acid	Generator

Chemical Formula

C₃₅H₄₃NO₁₀

Average Mass

637.7260 Da

Monoisotopic Mass

637.28870 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

CCCC(=O)OC1C2C(OC(=O)CC)C(C)CC2(OC(C)=O)C(=O)C2(C)OCC11C2C(C=CC1OC(=O)C1=CC=CN=C1)C(C)=C

InChI Identifier

InChI=1S/C35H43NO10/c1-8-11-26(39)45-30-27-28(44-25(38)9-2)20(5)16-35(27,46-21(6)37)32(41)33(7)29-23(19(3)4)13-14-24(34(29,30)18-42-33)43-31(40)22-12-10-15-36-17-22/h10,12-15,17,20,23-24,27-30H,3,8-9,11,16,18H2,1-2,4-7H3

InChI Key

MVADZRSXUXTRLD-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Euphorbia myrsinites	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tetracarboxylic acids and derivatives

Direct Parent

Tetracarboxylic acids and derivatives

Alternative Parents

Substituents

Tetracarboxylic acid or derivatives
Pyridine carboxylic acid
Pyridine carboxylic acid or derivatives
Fatty acid ester
Alpha-acyloxy ketone
Pyridine
Fatty acyl
Heteroaromatic compound
Tetrahydrofuran
Carboxylic acid ester
Ketone
Oxacycle
Ether
Dialkyl ether
Azacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Organic nitrogen 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	3.74	ALOGPS
logP	4.47	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Basic)	3.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	144.39 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	163.74 m³·mol⁻¹	ChemAxon
Polarizability	66.02 Å³	ChemAxon
Number of Rings	5	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate (NP0169636)

MOL for NP0169636 (7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate)

3D MOL for NP0169636 (7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate)

3D SDF for NP0169636 (7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate)

3D-SDF for NP0169636 (7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate)

PDB for NP0169636 (7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate)

3D PDB for NP0169636 (7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate)

SMILES for NP0169636 (7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate)

INCHI for NP0169636 (7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate)

Structure for NP0169636 (7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate)

3D Structure for NP0169636 (7-(acetyloxy)-2-(butanoyloxy)-5,9-dimethyl-8-oxo-11-(prop-1-en-2-yl)-4-(propanoyloxy)-16-oxatetracyclo[7.5.2.0¹,¹⁰.0³,⁷]hexadec-12-en-14-yl pyridine-3-carboxylate)