NP-MRD: Showing NP-Card for (9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate (NP0319208)

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Record Information

Version

2.0

Created at

2022-09-11 20:07:35 UTC

Updated at

2022-09-11 20:07:35 UTC

NP-MRD ID

NP0319208

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate

Description

(9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate is found in Euphorbia segetalis and Euphorbia terracina.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112222072D          

 60 63  0  0  0  0            999 V2000
    5.8485    1.1521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2922    1.7069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5512    2.5438    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8927    0.8582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5015    0.0076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3265    0.0111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1337    0.5690    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0560    0.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6055    1.4590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8377    0.1066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0426   -0.3985    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8178   -0.8311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8551   -0.0083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0461   -1.2235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4615   -1.9362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0520   -2.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8809   -2.9783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3392   -3.0679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9210   -3.8672    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5143   -3.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1910   -3.7156    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5098   -4.5798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7415   -5.4084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7620   -4.3542    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3461   -3.8790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5260   -3.9686    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7596   -4.3621    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3094   -4.9748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0030   -5.8672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3382   -6.6768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3047   -6.3746    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1873   -3.2163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2798   -3.5934    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4881   -4.1124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0145   -4.8378    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6263   -3.9491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7981   -2.6618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3826   -1.9490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6699   -2.3645    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9537   -1.9549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0916   -2.1310    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9503   -1.1299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6630   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3792   -1.1240    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9428   -0.3415    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9717   -0.1762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0960   -0.2468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1478    0.6782    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3500    0.8884    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1332    1.6844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7141    2.2702    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5119    2.0600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7287    1.2640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7887   -0.4078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9611    0.6136    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9385    1.6103    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2021    2.4659    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2293    2.1336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4252    1.6394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2886    3.0135    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  1  0  0  0  0
  8 10  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  1  0  0  0  0
 14 15  2  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  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  2  0  0  0  0
 26 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 32 37  1  0  0  0  0
 20 37  1  0  0  0  0
 37 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  1  0  0  0  0
 43 44  1  0  0  0  0
 38 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  2  0  0  0  0
 46 48  1  0  0  0  0
 48 49  2  0  0  0  0
 49 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 48 53  1  0  0  0  0
 44 54  1  0  0  0  0
  5 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  2  0  0  0  0
 56 58  1  0  0  0  0
 58 59  1  0  0  0  0
 58 60  1  0  0  0  0
M  END

     RDKit          3D

114117  0  0  0  0  0  0  0  0999 V2000
   -5.7584   -1.4190   -1.4498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6702   -0.4357   -1.3668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6234    0.5068   -2.1744 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7116   -0.5265   -0.4314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5970    0.3639   -0.2456 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3779   -0.3101   -0.6170 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7418   -1.1531   -1.7477 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3025   -0.9476   -3.0212 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5461    0.0233   -3.2760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6655   -1.8215   -4.1696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1111   -1.3020   -5.4738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1664   -1.8958   -4.2902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6257   -1.2388    0.3029 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7200   -0.7445    1.6096 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2317   -1.3338    2.7435 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3464   -2.4340    2.4663 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2756   -0.9171    4.1078 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2642   -0.2133    6.8418 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5619   -0.1250    0.9597 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3685    0.6088    0.4036 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.1102   -0.7063    1.8273 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3243    0.4724    1.4559 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309112222072D          

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 58 59  1  0  0  0  0
 58 60  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0319208

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)OC1C(OC(C)=O)C(OC(C)=O)C(C)(C)\C=C\C(C)C(=O)C2(CC(C)(OC(C)=O)C(OC(C)=O)C2C2OC(=O)CCC12OC(=O)C1=CC=CC=C1)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C43H54O17/c1-22(2)38(51)57-37-32(53-24(4)44)36(55-26(6)46)40(9,10)19-17-23(3)33(50)43(59-28(8)48)21-41(11,58-27(7)47)34(54-25(5)45)31(43)35-42(37,20-18-30(49)56-35)60-39(52)29-15-13-12-14-16-29/h12-17,19,22-23,31-32,34-37H,18,20-21H2,1-11H3/b19-17+

> <INCHI_KEY>
PPQIAMYTDKJYQS-HTXNQAPBSA-N

> <FORMULA>
C43H54O17

> <MOLECULAR_WEIGHT>
842.888

> <EXACT_MASS>
842.336100279

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
114

> <JCHEM_AVERAGE_POLARIZABILITY>
84.59605393134869

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(9E)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0^{2,6}]nonadec-9-en-15-yl benzoate

> <JCHEM_LOGP>
4.405048811999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.968086397842058

> <JCHEM_PKA_STRONGEST_BASIC>
-6.160130944942036

> <JCHEM_POLAR_SURFACE_AREA>
227.46999999999994

> <JCHEM_REFRACTIVITY>
203.9634

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(9E)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0^{2,6}]nonadec-9-en-15-yl benzoate

> <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      10.917   2.151   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.879   3.186   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.362   4.748   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       9.133   1.602   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       8.403   0.014   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.943   0.021   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      11.450   1.062   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      13.171   1.375   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.197   2.723   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      14.630   0.199   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      11.280  -0.744   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.727  -1.551   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.796  -0.015   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.286  -2.284   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.062  -3.614   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.297  -4.951   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.844  -5.559   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.967  -5.727   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.053  -7.219   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.427  -5.733   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       9.690  -6.936   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.285  -8.549   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.717 -10.096   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.889  -8.128   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.113  -7.241   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.582  -7.408   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.151  -8.142   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       6.178  -9.286   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       5.606 -10.952   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       6.231 -12.463   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.302 -11.899   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       5.950  -6.004   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.256  -6.708   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       2.778  -7.677   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       1.894  -9.031   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       1.169  -7.372   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       7.090  -4.969   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.314  -3.638   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       4.984  -4.414   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       3.647  -3.649   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       2.038  -3.978   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       3.640  -2.109   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.971  -1.334   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       6.308  -2.098   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       5.493  -0.638   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       3.681  -0.329   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       2.046  -0.461   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       4.009   1.266   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       2.520   1.658   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       2.115   3.144   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0       3.200   4.238   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       4.689   3.845   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       5.094   2.359   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       7.072  -0.761   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       7.394   1.145   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0       7.352   3.006   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0       7.844   4.603   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0       6.028   3.983   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0       4.527   3.060   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0       6.139   5.625   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   54                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   25   37                                             
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   20   26                                                       
CONECT   26   25   27   28   32                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   26   33   37                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   32   20   38                                                  
CONECT   38   37   39   44                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   38   45   54                                             
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49   53                                                  
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   48                                                       
CONECT   54   44    5   55                                                  
CONECT   55   54   56                                                       
CONECT   56   55   57   58                                                  
CONECT   57   56                                                            
CONECT   58   56   59   60                                                  
CONECT   59   58                                                            
CONECT   60   58                                                            
MASTER        0    0    0    0    0    0    0    0   60    0  126    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₃H₅₄O₁₇

Average Mass

842.8880 Da

Monoisotopic Mass

842.33610 Da

IUPAC Name

(9E)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0^{2,6}]nonadec-9-en-15-yl benzoate

Traditional Name

(9E)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0^{2,6}]nonadec-9-en-15-yl benzoate

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)OC1C(OC(C)=O)C(OC(C)=O)C(C)(C)\C=C\C(C)C(=O)C2(CC(C)(OC(C)=O)C(OC(C)=O)C2C2OC(=O)CCC12OC(=O)C1=CC=CC=C1)OC(C)=O

InChI Identifier

InChI=1S/C43H54O17/c1-22(2)38(51)57-37-32(53-24(4)44)36(55-26(6)46)40(9,10)19-17-23(3)33(50)43(59-28(8)48)21-41(11,58-27(7)47)34(54-25(5)45)31(43)35-42(37,20-18-30(49)56-35)60-39(52)29-15-13-12-14-16-29/h12-17,19,22-23,31-32,34-37H,18,20-21H2,1-11H3/b19-17+

InChI Key

PPQIAMYTDKJYQS-HTXNQAPBSA-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 segetalis	LOTUS Database	35616633
Euphorbia terracina	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	4.41	ChemAxon
pKa (Strongest Acidic)	14.97	ChemAxon
pKa (Strongest Basic)	-6.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	227.47 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	203.96 m³·mol⁻¹	ChemAxon
Polarizability	84.6 Å³	ChemAxon
Number of Rings	4	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate (NP0319208)

MOL for NP0319208 ((9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate)

3D MOL for NP0319208 ((9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate)

3D SDF for NP0319208 ((9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate)

3D-SDF for NP0319208 ((9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate)

PDB for NP0319208 ((9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate)

3D PDB for NP0319208 ((9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate)

SMILES for NP0319208 ((9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate)

INCHI for NP0319208 ((9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate)

Structure for NP0319208 ((9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate)

3D Structure for NP0319208 ((9e)-3,4,6,12,13-pentakis(acetyloxy)-4,8,11,11-tetramethyl-14-[(2-methylpropanoyl)oxy]-7,18-dioxo-19-oxatricyclo[13.4.0.0²,⁶]nonadec-9-en-15-yl benzoate)