NP-MRD: Showing NP-Card for Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate (NP0010604)

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Record Information

Version

2.0

Created at

2021-01-05 20:04:11 UTC

Updated at

2021-07-15 17:06:34 UTC

NP-MRD ID

NP0010604

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate

Provided By

NPAtlas

Description

Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate is found in Penicillium solitum. Based on a literature review very few articles have been published on Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107393D          

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M  END

     RDKit          3D

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M  END


  Mrv1652306242107393D          

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    9.0483    0.2201   -0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.6662    0.4432    1.0813 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3381    0.3044    1.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5630    0.4004   -0.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9886   -2.0769    1.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2299   -2.0687   -0.1390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8485   -2.1621    0.4905 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0892   -0.6788    1.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5320   -0.8517   -1.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6022    0.6379   -0.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1795   -1.0582   -0.9602 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4896    0.5064   -1.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763    0.0178    1.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8078    1.5543    0.5929 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.4321    4.0240   -0.9421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0764    5.1716   -0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.2507   -2.5591    0.5258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5912   -3.1574    2.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3  0  0  0
  2  3  1  0  0  0  0
  3  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
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
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 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
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 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
  1 28  1  0  0  0  0
  1 29  1  0  0  0  0
  2 30  1  0  0  0  0
  3 31  1  0  0  0  0
  3 32  1  0  0  0  0
  4 33  1  0  0  0  0
  4 34  1  0  0  0  0
  5 35  1  0  0  0  0
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  6 37  1  0  0  0  0
  6 38  1  0  0  0  0
  7 39  1  0  0  0  0
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  8 41  1  0  0  0  0
  8 42  1  0  0  0  0
  9 43  1  0  0  0  0
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 11 47  1  1  0  0  0
 15 48  1  0  0  0  0
 15 49  1  0  0  0  0
 15 50  1  0  0  0  0
 17 51  1  0  0  0  0
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 19 54  1  0  0  0  0
 19 55  1  0  0  0  0
 23 56  1  0  0  0  0
 23 57  1  0  0  0  0
 23 58  1  0  0  0  0
 27 59  1  0  0  0  0
 27 60  1  0  0  0  0
 27 61  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0010604

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O[C@@](C(=O)OC([H])([H])[H])(C([H])([H])C([H])([H])C(=O)OC([H])([H])[H])[C@@]([H])(C(=O)OC([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])=C([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C20H34O7/c1-5-6-7-8-9-10-11-12-13-16(18(22)26-3)20(24,19(23)27-4)15-14-17(21)25-2/h5,16,24H,1,6-15H2,2-4H3/t16-,20+/m1/s1

> <INCHI_KEY>
PYMFODJLNHATSF-QRIPLOBPSA-N

> <FORMULA>
C20H34O7

> <MOLECULAR_WEIGHT>
386.485

> <EXACT_MASS>
386.230453435

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
43.2656019592049

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,2,4-trimethyl (1S,2S)-1-(dec-9-en-1-yl)-2-hydroxybutane-1,2,4-tricarboxylate

> <ALOGPS_LOGP>
3.46

> <JCHEM_LOGP>
3.6437721979999997

> <ALOGPS_LOGS>
-4.87

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.895754515261832

> <JCHEM_PKA_STRONGEST_BASIC>
-4.156596975024475

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
100.71379999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
18

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.22e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,2,4-trimethyl (1S,2S)-1-(dec-9-en-1-yl)-2-hydroxybutane-1,2,4-tricarboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 61 60  0  0  0  0  0  0  0  0999 V2000
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    1.8078    1.5543    0.5929 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2120   -3.2074   -2.3357 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.5912   -3.1574    2.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 11 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 16 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
  9 44  1  0
 10 45  1  0
 10 46  1  0
 11 47  1  1
 15 48  1  0
 15 49  1  0
 15 50  1  0
 17 51  1  0
 18 52  1  0
 18 53  1  0
 19 54  1  0
 19 55  1  0
 23 56  1  0
 23 57  1  0
 23 58  1  0
 27 59  1  0
 27 60  1  0
 27 61  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0       8.647  -0.738  -0.905  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.678  -1.268  -0.179  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.135  -0.525   0.986  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.662  -0.237   0.849  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.858  -1.511   0.728  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.377  -1.201   0.594  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.124  -0.366  -0.631  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.630  -0.053  -0.814  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.118   0.699   0.351  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.309   1.135   0.351  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.308   0.067   0.285  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.230  -0.718  -0.953  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.082  -0.174  -2.091  0.00  0.00           O+0
HETATM   14  O   UNK     0      -1.315  -2.111  -0.986  0.00  0.00           O+0
HETATM   15  C   UNK     0      -1.242  -2.833  -2.188  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.718   0.502   0.580  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.783   1.039   1.888  0.00  0.00           O+0
HETATM   18  C   UNK     0      -3.268   1.516  -0.354  0.00  0.00           C+0
HETATM   19  C   UNK     0      -4.693   1.820   0.113  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.333   2.831  -0.763  0.00  0.00           C+0
HETATM   21  O   UNK     0      -4.794   3.364  -1.745  0.00  0.00           O+0
HETATM   22  O   UNK     0      -6.633   3.199  -0.451  0.00  0.00           O+0
HETATM   23  C   UNK     0      -7.361   4.153  -1.204  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.593  -0.693   0.569  0.00  0.00           C+0
HETATM   25  O   UNK     0      -3.747  -1.331  -0.503  0.00  0.00           O+0
HETATM   26  O   UNK     0      -4.257  -1.139   1.705  0.00  0.00           O+0
HETATM   27  C   UNK     0      -5.067  -2.284   1.592  0.00  0.00           C+0
HETATM   28  H   UNK     0       9.048   0.220  -0.667  0.00  0.00           H+0
HETATM   29  H   UNK     0       9.046  -1.289  -1.765  0.00  0.00           H+0
HETATM   30  H   UNK     0       7.245  -2.245  -0.395  0.00  0.00           H+0
HETATM   31  H   UNK     0       7.269  -1.157   1.896  0.00  0.00           H+0
HETATM   32  H   UNK     0       7.666   0.443   1.081  0.00  0.00           H+0
HETATM   33  H   UNK     0       5.338   0.304   1.753  0.00  0.00           H+0
HETATM   34  H   UNK     0       5.563   0.400  -0.066  0.00  0.00           H+0
HETATM   35  H   UNK     0       4.989  -2.077   1.671  0.00  0.00           H+0
HETATM   36  H   UNK     0       5.230  -2.069  -0.139  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.849  -2.162   0.491  0.00  0.00           H+0
HETATM   38  H   UNK     0       3.089  -0.679   1.544  0.00  0.00           H+0
HETATM   39  H   UNK     0       3.532  -0.852  -1.515  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.602   0.638  -0.541  0.00  0.00           H+0
HETATM   41  H   UNK     0       1.180  -1.058  -0.960  0.00  0.00           H+0
HETATM   42  H   UNK     0       1.490   0.506  -1.769  0.00  0.00           H+0
HETATM   43  H   UNK     0       1.276   0.018   1.260  0.00  0.00           H+0
HETATM   44  H   UNK     0       1.808   1.554   0.593  0.00  0.00           H+0
HETATM   45  H   UNK     0      -0.431   1.816  -0.554  0.00  0.00           H+0
HETATM   46  H   UNK     0      -0.429   1.829   1.219  0.00  0.00           H+0
HETATM   47  H   UNK     0      -1.071  -0.678   1.115  0.00  0.00           H+0
HETATM   48  H   UNK     0      -0.212  -3.207  -2.336  0.00  0.00           H+0
HETATM   49  H   UNK     0      -1.607  -2.265  -3.062  0.00  0.00           H+0
HETATM   50  H   UNK     0      -1.900  -3.723  -2.095  0.00  0.00           H+0
HETATM   51  H   UNK     0      -2.483   0.302   2.484  0.00  0.00           H+0
HETATM   52  H   UNK     0      -3.339   1.159  -1.401  0.00  0.00           H+0
HETATM   53  H   UNK     0      -2.735   2.503  -0.297  0.00  0.00           H+0
HETATM   54  H   UNK     0      -4.585   2.301   1.119  0.00  0.00           H+0
HETATM   55  H   UNK     0      -5.281   0.912   0.248  0.00  0.00           H+0
HETATM   56  H   UNK     0      -7.223   4.010  -2.298  0.00  0.00           H+0
HETATM   57  H   UNK     0      -8.432   4.024  -0.942  0.00  0.00           H+0
HETATM   58  H   UNK     0      -7.076   5.172  -0.880  0.00  0.00           H+0
HETATM   59  H   UNK     0      -6.071  -2.079   2.047  0.00  0.00           H+0
HETATM   60  H   UNK     0      -5.251  -2.559   0.526  0.00  0.00           H+0
HETATM   61  H   UNK     0      -4.591  -3.157   2.116  0.00  0.00           H+0
CONECT    1    2   28   29                                                  
CONECT    2    1    3   30                                                  
CONECT    3    2    4   31   32                                             
CONECT    4    3    5   33   34                                             
CONECT    5    4    6   35   36                                             
CONECT    6    5    7   37   38                                             
CONECT    7    6    8   39   40                                             
CONECT    8    7    9   41   42                                             
CONECT    9    8   10   43   44                                             
CONECT   10    9   11   45   46                                             
CONECT   11   10   12   16   47                                             
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   48   49   50                                             
CONECT   16   11   17   18   24                                             
CONECT   17   16   51                                                       
CONECT   18   16   19   52   53                                             
CONECT   19   18   20   54   55                                             
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   56   57   58                                             
CONECT   24   16   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   59   60   61                                             
CONECT   28    1                                                            
CONECT   29    1                                                            
CONECT   30    2                                                            
CONECT   31    3                                                            
CONECT   32    3                                                            
CONECT   33    4                                                            
CONECT   34    4                                                            
CONECT   35    5                                                            
CONECT   36    5                                                            
CONECT   37    6                                                            
CONECT   38    6                                                            
CONECT   39    7                                                            
CONECT   40    7                                                            
CONECT   41    8                                                            
CONECT   42    8                                                            
CONECT   43    9                                                            
CONECT   44    9                                                            
CONECT   45   10                                                            
CONECT   46   10                                                            
CONECT   47   11                                                            
CONECT   48   15                                                            
CONECT   49   15                                                            
CONECT   50   15                                                            
CONECT   51   17                                                            
CONECT   52   18                                                            
CONECT   53   18                                                            
CONECT   54   19                                                            
CONECT   55   19                                                            
CONECT   56   23                                                            
CONECT   57   23                                                            
CONECT   58   23                                                            
CONECT   59   27                                                            
CONECT   60   27                                                            
CONECT   61   27                                                            
MASTER        0    0    0    0    0    0    0    0   61    0  120    0
END

RDKit          3D

61 60  0  0  0  0  0  0  0  0999 V2000
    8.6468   -0.7375   -0.9045 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6775   -1.2677   -0.1789 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1351   -0.5247    0.9858 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6616   -0.2372    0.8488 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8579   -1.5112    0.7283 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3774   -1.2014    0.5941 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1243   -0.3656   -0.6305 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6300   -0.0534   -0.8137 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1184    0.6989    0.3507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3088    1.1352    0.3509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3075    0.0668    0.2846 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2299   -0.7176   -0.9534 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0824   -0.1740   -2.0914 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3154   -2.1112   -0.9855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2422   -2.8333   -2.1880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7176    0.5018    0.5801 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7826    1.0389    1.8883 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2677    1.5158   -0.3538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6927    1.8202    0.1126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3332    2.8307   -0.7633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7940    3.3635   -1.7450 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6328    3.1993   -0.4510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3614    4.1530   -1.2041 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5934   -0.6925    0.5690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7469   -1.3305   -0.5032 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2567   -1.1386    1.7048 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0667   -2.2843    1.5920 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0483    0.2201   -0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0462   -1.2890   -1.7654 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2448   -2.2447   -0.3949 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2689   -1.1572    1.8959 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6662    0.4432    1.0813 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3381    0.3044    1.7529 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5630    0.4004   -0.0656 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9886   -2.0769    1.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2299   -2.0687   -0.1390 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8485   -2.1621    0.4905 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0892   -0.6788    1.5439 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5320   -0.8517   -1.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6022    0.6379   -0.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1795   -1.0582   -0.9602 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4896    0.5064   -1.7691 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2763    0.0178    1.2600 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8078    1.5543    0.5929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4305    1.8159   -0.5536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4293    1.8287    1.2191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0714   -0.6780    1.1149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2120   -3.2074   -2.3357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6067   -2.2646   -3.0624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9001   -3.7225   -2.0948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4829    0.3018    2.4840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3389    1.1588   -1.4015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7349    2.5035   -0.2966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5855    2.3013    1.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2806    0.9118    0.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2227    4.0098   -2.2979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4321    4.0240   -0.9421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0764    5.1716   -0.8796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0705   -2.0788    2.0467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2507   -2.5591    0.5258 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5912   -3.1574    2.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 14 15  1  0
 11 16  1  0
 16 17  1  1
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 16 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  0
  6 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
  9 44  1  0
 10 45  1  0
 10 46  1  0
 11 47  1  1
 15 48  1  0
 15 49  1  0
 15 50  1  0
 17 51  1  0
 18 52  1  0
 18 53  1  0
 19 54  1  0
 19 55  1  0
 23 56  1  0
 23 57  1  0
 23 58  1  0
 27 59  1  0
 27 60  1  0
 27 61  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Value	Source
Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoic acid	Generator
1,2,4-Trimethyl (1S)-1-(dec-9-en-1-yl)-2-hydroxybutane-1,2,4-tricarboxylic acid	Generator

Chemical Formula

C₂₀H₃₄O₇

Average Mass

386.4850 Da

Monoisotopic Mass

386.23045 Da

IUPAC Name

1,2,4-trimethyl (1S,2S)-1-(dec-9-en-1-yl)-2-hydroxybutane-1,2,4-tricarboxylate

Traditional Name

1,2,4-trimethyl (1S,2S)-1-(dec-9-en-1-yl)-2-hydroxybutane-1,2,4-tricarboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)CCC(O)([C@H](CCCCCCCCC=C)C(=O)OC)C(=O)OC

InChI Identifier

InChI=1S/C20H34O7/c1-5-6-7-8-9-10-11-12-13-16(18(22)26-3)20(24,19(23)27-4)15-14-17(21)25-2/h5,16,24H,1,6-15H2,2-4H3/t16-,20?/m1/s1

InChI Key

PYMFODJLNHATSF-QRIPLOBPSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Penicillium solitum	NPAtlas	22276851

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Fatty acid methyl ester
Fatty acid ester
Fatty acyl
Methyl ester
Tertiary alcohol
Carboxylic acid ester
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	3.46	ALOGPS
logP	3.64	ChemAxon
logS	-4.9	ALOGPS
pKa (Strongest Acidic)	11.9	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	99.13 Å²	ChemAxon
Rotatable Bond Count	18	ChemAxon
Refractivity	100.71 m³·mol⁻¹	ChemAxon
Polarizability	43.27 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA012458

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78437750

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139586565

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate (NP0010604)

MOL for NP0010604 (Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate)

3D MOL for NP0010604 (Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate)

3D SDF for NP0010604 (Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate)

3D-SDF for NP0010604 (Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate)

PDB for NP0010604 (Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate)

3D PDB for NP0010604 (Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate)

SMILES for NP0010604 (Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate)

INCHI for NP0010604 (Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate)

Structure for NP0010604 (Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate)

3D Structure for NP0010604 (Trimethyl 4-hydroxy-4,5-dicarboxy-14-pentadecenoate)