NP-MRD: Showing NP-Card for (1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate (NP0253482)

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Record Information

Version

2.0

Created at

2022-09-07 17:21:26 UTC

Updated at

2022-09-07 17:21:26 UTC

NP-MRD ID

NP0253482

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate

Description

(1R,2R,3R,4S,5S,12R,15R,16R)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]Hexadec-13-en-2-yl benzoate belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups. (1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate is found in Euphorbia cheiradenia. Based on a literature review very few articles have been published on (1R,2R,3R,4S,5S,12R,15R,16R)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]Hexadec-13-en-2-yl benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072219212D          

 44 48  0  0  1  0            999 V2000
    0.6910    2.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1735    1.6537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9943    1.7370    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8353    0.9012    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3178    0.2320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9795   -0.5204    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2950    0.0145    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4209    0.8298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2223    1.3465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0964    2.1618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9914    1.0478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4780   -0.2738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6149   -1.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0213   -1.6127    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7943   -1.3244    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3073   -1.9705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8514   -2.6580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0566   -2.4369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2544   -3.2010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1323   -1.9722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6001   -0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0002    1.0649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6738    0.5886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0758    1.8864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2613    1.1565    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4423    1.8970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7304    3.1360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1594    3.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1577    2.3080    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
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  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
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 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 39 44  1  0  0  0  0
M  END

     RDKit          3D

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   -0.5750    2.6317   -3.5828 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7942    1.0576   -1.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4223    0.7511    3.2644 C   0  0  0  0  0  0  0  0  0  0  0  0
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 17 60  1  0
M  END


  Mrv1652309072219212D          

 44 48  0  0  1  0            999 V2000
    0.6910    2.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1735    1.6537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.9795   -0.5204    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2950    0.0145    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4209    0.8298    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2223    1.3465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0964    2.1618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9914    1.0478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4780   -0.2738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6149   -1.0874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0213   -1.6127    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7943   -1.3244    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3073   -1.9705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6968   -2.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -2.6580    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0566   -2.4369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2544   -3.2010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7581   -2.5667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1323   -1.9722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4887   -2.7162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6480   -1.3282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9707   -2.0875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4696   -1.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7954   -0.6460    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6001   -0.4640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1752   -0.1019    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2509    0.7197    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0002    1.0649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6738    0.5886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0758    1.8864    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4661   -0.5235    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7236   -0.1640    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7253    0.6610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4406    1.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2613    1.1565    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4423    1.8970    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7287    2.3110    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7304    3.1360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4458    3.5470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1594    3.1330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1577    2.3080    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
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  7 12  1  0  0  0  0
 12 13  2  0  0  0  0
 14 13  1  6  0  0  0
 15 14  1  6  0  0  0
  6 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
 34 29  1  1  0  0  0
 24 34  1  0  0  0  0
 34 35  1  0  0  0  0
  6 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 43 44  2  0  0  0  0
 39 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0253482

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@H]1CC2(O)[C@H]([C@H]1OC(C)=O)[C@@H](OC(=O)C1=CC=CC=C1)[C@@]1(COC(C)=O)[C@H]3[C@@H](C=C[C@H]1OC(C)=O)C(C)(C)OC3(C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C33H40O11/c1-17-15-33(39)24(25(17)42-20(4)36)27(43-28(37)21-11-9-8-10-12-21)32(16-40-18(2)34)23(41-19(3)35)14-13-22-26(32)31(7,29(33)38)44-30(22,5)6/h8-14,17,22-27,39H,15-16H2,1-7H3/t17-,22+,23+,24+,25-,26-,27+,31?,32+,33?/m0/s1

> <INCHI_KEY>
PGEIXGCPAXFUOK-NIXPRAFHSA-N

> <FORMULA>
C33H40O11

> <MOLECULAR_WEIGHT>
612.672

> <EXACT_MASS>
612.257062108

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
62.09807738805433

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,4S,5S,12R,15R,16R)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0^{3,7}.0^{12,16}]hexadec-13-en-2-yl benzoate

> <JCHEM_LOGP>
2.7956908936666673

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.585624687894121

> <JCHEM_PKA_STRONGEST_BASIC>
-3.854847761515111

> <JCHEM_POLAR_SURFACE_AREA>
151.73

> <JCHEM_REFRACTIVITY>
154.02139999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,4S,5S,12R,15R,16R)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0^{3,7}.0^{12,16}]hexadec-13-en-2-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       1.290   4.336   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.191   3.087   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.723   3.242   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.559   1.682   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.460   0.433   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.828  -0.972   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.551   0.027   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.786   1.549   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.415   2.513   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.180   4.035   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.851   1.956   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -0.892  -0.511   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.148  -2.030   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.040  -3.010   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.483  -2.472   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.440  -3.678   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.167  -5.036   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       1.589  -4.962   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.106  -4.549   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.475  -5.975   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.415  -4.791   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.980  -3.681   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.646  -5.070   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       4.943  -2.479   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.545  -3.897   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       6.477  -2.621   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.085  -1.206   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.587  -0.866   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.927  -0.190   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.068   1.343   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.467   1.988   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.724   1.099   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       7.608   3.521   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.603  -0.977   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.217  -0.306   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       3.221   1.234   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       4.556   2.001   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       6.088   2.159   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       4.559   3.541   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       3.227   4.314   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.230   5.854   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       4.565   6.621   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.898   5.848   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       5.894   4.308   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                                                       
CONECT    6    5    7   15   35                                             
CONECT    7    6    8   12                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    7   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14    6   16                                                  
CONECT   16   15   17   18   22                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   14   20   21                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   16   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26   34                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34   29   24   35                                                  
CONECT   35   34    6   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   44                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   39                                                       
MASTER        0    0    0    0    0    0    0    0   44    0   96    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,3R,4S,5S,12R,15R,16R)-4,15-Bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0,.0,]hexadec-13-en-2-yl benzoic acid	Generator

Chemical Formula

C₃₃H₄₀O₁₁

Average Mass

612.6720 Da

Monoisotopic Mass

612.25706 Da

IUPAC Name

(1R,2R,3R,4S,5S,12R,15R,16R)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0^{3,7}.0^{12,16}]hexadec-13-en-2-yl benzoate

Traditional Name

(1R,2R,3R,4S,5S,12R,15R,16R)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0^{3,7}.0^{12,16}]hexadec-13-en-2-yl benzoate

CAS Registry Number

Not Available

SMILES

C[C@H]1CC2(O)[C@H]([C@H]1OC(C)=O)[C@@H](OC(=O)C1=CC=CC=C1)[C@@]1(COC(C)=O)[C@H]3[C@@H](C=C[C@H]1OC(C)=O)C(C)(C)OC3(C)C2=O

InChI Identifier

InChI=1S/C33H40O11/c1-17-15-33(39)24(25(17)42-20(4)36)27(43-28(37)21-11-9-8-10-12-21)32(16-40-18(2)34)23(41-19(3)35)14-13-22-26(32)31(7,29(33)38)44-30(22,5)6/h8-14,17,22-27,39H,15-16H2,1-7H3/t17-,22+,23+,24+,25-,26-,27+,31?,32+,33?/m0/s1

InChI Key

PGEIXGCPAXFUOK-NIXPRAFHSA-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 cheiradenia	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
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Benzenoid
Monocyclic benzene moiety
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	2.8	ChemAxon
pKa (Strongest Acidic)	12.59	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	151.73 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	154.02 m³·mol⁻¹	ChemAxon
Polarizability	62.1 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163189084

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate (NP0253482)

MOL for NP0253482 ((1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate)

3D MOL for NP0253482 ((1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate)

3D SDF for NP0253482 ((1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate)

3D-SDF for NP0253482 ((1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate)

PDB for NP0253482 ((1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate)

3D PDB for NP0253482 ((1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate)

SMILES for NP0253482 ((1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate)

INCHI for NP0253482 ((1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate)

Structure for NP0253482 ((1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate)

3D Structure for NP0253482 ((1r,2r,3r,4s,5s,12r,15r,16r)-4,15-bis(acetyloxy)-1-[(acetyloxy)methyl]-7-hydroxy-5,9,11,11-tetramethyl-8-oxo-10-oxatetracyclo[7.6.1.0³,⁷.0¹²,¹⁶]hexadec-13-en-2-yl benzoate)