NP-MRD: Showing NP-Card for methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate (NP0220702)

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Record Information

Version

2.0

Created at

2022-09-05 22:05:22 UTC

Updated at

2022-09-05 22:05:22 UTC

NP-MRD ID

NP0220702

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate

Description

Methyl (9R,12S,13S)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate is found in Wedelia acapulcensis. Based on a literature review very few articles have been published on methyl (9R,12S,13S)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062200052D          

 33 32  0  0  1  0            999 V2000
   15.6980    5.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4776    5.3839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6335    4.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0099    4.0337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2303    4.3038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6067    3.7637    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.7626    2.9535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5421    2.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6980    1.8734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1658    3.2236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8271    4.0337    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.2035    3.4936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4239    3.7637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8003    3.2236    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0207    3.4936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3971    2.9535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6175    3.2236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9939    2.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2143    2.9535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5907    2.4135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8111    2.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3434    1.3333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4079    2.4135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7843    1.8734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9562    2.4135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7357    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3594    2.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8916    1.3333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6712    4.8439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8916    5.1139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2680    4.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7357    5.9240    0.0000 O   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  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  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
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 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
 14 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 11 30  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
M  END

     RDKit          3D

 73 72  0  0  0  0  0  0  0  0999 V2000
   -8.5129   -1.0547   -1.6535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0003   -1.2197   -1.3703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8480   -0.9959    0.0701 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.3424    0.9072   -0.2101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8859    0.8568    0.1558 C   0  0  2  0  0  0  0  0  0  0  0  0
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    0.4736   -0.2037    0.8383 C   0  0  1  0  0  0  0  0  0  0  0  0
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    3.4337   -0.6503    0.8235 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7335   -1.1075   -0.5797 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6446   -0.1984   -1.3475 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9940   -0.0113   -0.7017 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8368    0.9007   -1.6009 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1586    1.1198   -0.9903 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2295    1.5055    0.1914 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3438    0.9011   -1.7058 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.5683    1.1341   -1.0492 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1946    0.0815    2.1843 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3676   -0.8658    3.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0932   -0.6224    4.6026 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7798   -2.0289    2.8840 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7538   -2.2939   -1.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3817   -2.9568   -0.5494 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.8578    1.2076    1.2509 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6186    4.7360   -0.0699 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.0175   -1.1995    0.7388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8596   -0.9395    1.7796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9170    0.2422   -0.8425 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8727   -1.2324    0.7703 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0386    1.7739    0.1012 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5935    0.3455   -0.8521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4751    1.4312    0.4736 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5964    1.0092    1.9443 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4538   -0.4945    1.2943 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309062200052D          

 33 32  0  0  1  0            999 V2000
   15.6980    5.6540    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4776    5.3839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.6335    4.5738    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0099    4.0337    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2303    4.3038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6067    3.7637    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.7626    2.9535    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.5421    2.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6980    1.8734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1658    3.2236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8271    4.0337    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.2035    3.4936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4239    3.7637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8003    3.2236    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.0207    3.4936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3971    2.9535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6175    3.2236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9939    2.6835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.1875    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3434    1.3333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4079    2.4135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7843    1.8734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9562    2.4135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   12.8916    1.3333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   12.7357    5.9240    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
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  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
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 31 32  1  0  0  0  0
 31 33  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0220702

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC\C=C/C[C@H](OC(C)=O)[C@@H](OC(C)=O)\C=C\[C@@H](CCCCCCCC(=O)OC)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H40O8/c1-6-7-11-15-23(32-20(3)27)24(33-21(4)28)18-17-22(31-19(2)26)14-12-9-8-10-13-16-25(29)30-5/h7,11,17-18,22-24H,6,8-10,12-16H2,1-5H3/b11-7-,18-17+/t22-,23+,24+/m1/s1

> <INCHI_KEY>
PQQKAKFNGYAFMM-GTUZTZDDSA-N

> <FORMULA>
C25H40O8

> <MOLECULAR_WEIGHT>
468.587

> <EXACT_MASS>
468.272318248

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
52.242814718498266

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (9R,10E,12S,13S,15Z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate

> <JCHEM_LOGP>
4.354621340333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.414432506687329

> <JCHEM_POLAR_SURFACE_AREA>
105.20000000000002

> <JCHEM_REFRACTIVITY>
125.13489999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
21

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl (9R,10E,12S,13S,15Z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      29.303  10.554   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      30.758  10.050   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      31.049   8.538   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      29.885   7.530   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      28.430   8.034   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      27.266   7.026   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      27.557   5.513   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      29.012   5.009   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      29.303   3.497   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      30.176   6.017   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      25.811   7.530   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      24.646   6.521   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      23.191   7.026   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      22.027   6.017   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      20.572   6.521   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      19.408   5.513   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.953   6.017   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      16.789   5.009   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      15.333   5.513   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      14.169   4.505   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.714   5.009   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      11.550   4.001   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.841   2.489   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      10.095   4.505   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       8.931   3.497   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      22.318   4.505   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      23.773   4.001   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      24.938   5.009   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      24.064   2.489   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      25.520   9.042   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      24.064   9.546   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      22.900   8.538   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      23.773  11.058   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12   30                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   26                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24                                                            
CONECT   26   14   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   11   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   64    0
END

View in JSmol

Synonyms

Value	Source
Methyl (9R,12S,13S)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoic acid	Generator

Chemical Formula

C₂₅H₄₀O₈

Average Mass

468.5870 Da

Monoisotopic Mass

468.27232 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC\C=C/C[C@H](OC(C)=O)[C@@H](OC(C)=O)\C=C\[C@@H](CCCCCCCC(=O)OC)OC(C)=O

InChI Identifier

InChI=1S/C25H40O8/c1-6-7-11-15-23(32-20(3)27)24(33-21(4)28)18-17-22(31-19(2)26)14-12-9-8-10-13-16-25(29)30-5/h7,11,17-18,22-24H,6,8-10,12-16H2,1-5H3/b11-7-,18-17+/t22-,23+,24+/m1/s1

InChI Key

PQQKAKFNGYAFMM-GTUZTZDDSA-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
Wedelia acapulcensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Lineolic acids and derivatives

Direct Parent

Lineolic acids and derivatives

Alternative Parents

Substituents

Octadecanoid
Tetracarboxylic acid or derivatives
Fatty alcohol ester
Fatty acid methyl ester
Fatty acid ester
Methyl ester
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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

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

163030925

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate (NP0220702)

MOL for NP0220702 (methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate)

3D MOL for NP0220702 (methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate)

3D SDF for NP0220702 (methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate)

3D-SDF for NP0220702 (methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate)

PDB for NP0220702 (methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate)

3D PDB for NP0220702 (methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate)

SMILES for NP0220702 (methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate)

INCHI for NP0220702 (methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate)

Structure for NP0220702 (methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate)

3D Structure for NP0220702 (methyl (9r,10e,12s,13s,15z)-9,12,13-tris(acetyloxy)octadeca-10,15-dienoate)