NP-MRD: Showing NP-Card for (1E,22Z)-1,22-Diferuloyloxydocosane (NP0079700)

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Record Information

Version

2.0

Created at

2022-04-29 00:42:04 UTC

Updated at

2022-04-29 00:42:04 UTC

NP-MRD ID

NP0079700

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1E,22Z)-1,22-Diferuloyloxydocosane

Description

22-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}docosyl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring. (1E,22Z)-1,22-Diferuloyloxydocosane is found in Garcinia multiflora . Based on a literature review very few articles have been published on 22-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}docosyl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292202422D          

 50 51  0  0  0  0            999 V2000
   15.7184   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.1512   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.5801   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.2946   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.0091   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.7235   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   36.4380   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.4380   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   37.1525   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8670   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8670   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.5814   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.5814   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8670   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.1525   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.1525   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8670   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   39.2959   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   39.2959   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  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  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 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
 42 45  1  0  0  0  0
 41 46  1  0  0  0  0
 46 47  1  0  0  0  0
  3 48  1  0  0  0  0
 48 49  1  0  0  0  0
  2 50  1  0  0  0  0
M  END

     RDKit          3D

112113  0  0  0  0  0  0  0  0999 V2000
    9.7819   -2.2960    0.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8655   -1.7775    1.3767 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.7403   -0.8109    0.9663 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5802   -0.2405   -0.2979 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3933    0.7220   -0.7837 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2815    1.4936   -1.9940 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2105    1.8733   -2.5547 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8557    1.6759   -2.1625 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9170    2.1348   -2.9571 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3200    1.0788   -1.0555 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9757    0.9232   -0.7173 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2606    0.1068   -1.7359 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7740   -0.0544   -1.3627 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1638   -0.8709   -2.4502 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7448   -1.1812   -2.4301 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1668   -2.0756   -1.4039 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3671   -1.7051   -0.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6072   -2.5333    0.9576 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1550   -2.4734    1.0593 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2514   -2.7523   -0.0570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2041   -2.6640    0.4767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4920   -1.3059    1.0702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2648   -0.1666    0.1163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5625    1.1354    0.7944 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0052    1.2138    1.1855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3159    2.5338    1.8738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7154    2.6941    2.2281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8042    2.6845    1.2081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7385    3.6761    0.1246 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8146    3.6085   -0.9942 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0308    2.7847   -2.1797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3465    1.3509   -2.0474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6141    1.2525   -1.4249 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3067    0.1254   -1.1181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8013   -0.9812   -1.3941 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6125    0.2794   -0.4807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3868   -0.7217   -0.1381 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6897   -0.5870    0.4963 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2719    0.6084    0.8270 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5134    0.6848    1.4258 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2059   -0.4694    1.7083 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.4530   -0.3847    2.3097 O   0  0  0  0  0  0  0  0  0  0  0  0
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  -12.7288   -4.0856    1.3233 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4264   -1.7218    0.8011 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4499    1.1271    0.0818 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5996    0.5620    1.3160 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7618   -0.4117    1.7952 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9437   -0.9654    3.0630 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8583   -1.7255    0.7544 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0022   -2.4692   -0.4088 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5632   -3.3108    1.1022 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8166   -0.6489   -0.9514 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.2672    1.7822   -2.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3458    2.4560   -3.5077 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9491    0.4400    0.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5536    1.9444   -0.5952 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2420    0.6255   -2.7051 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7043   -0.8998   -1.7718 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3204    0.9767   -1.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7341   -1.8733   -2.5353 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4651   -0.4082   -3.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1853   -0.1832   -2.4409 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.1234   -2.2995   -1.7375 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.4644   -2.0106    0.2330 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3534   -0.6188    0.2140 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9983   -3.6017    0.8213 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0389   -2.2891    1.9888 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8770   -1.4774    1.5800 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8596   -3.2018    1.8962 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2127   -1.9931   -0.8786 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3582   -3.7905   -0.4129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8800   -2.7950   -0.3934 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.5927   -1.3158    1.3089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2199   -0.1600   -0.2707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9913   -0.2736   -0.7303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9829    1.1543    1.7684 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.1468    2.9462   -2.8911 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.4611    0.9801   -3.1415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5862    0.6803   -1.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0110    1.2782   -0.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9945   -1.7103   -0.3582 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7696    1.5412    0.6270 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.9468    1.6618    1.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.9524   -1.2245    2.5140 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.4217   -4.8859    1.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5110   -4.1324    0.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7698   -4.2577    1.8533 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0046   -2.6869    0.5580 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.1214    1.9025   -0.2946 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.4212    0.9002    1.9490 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3541   -1.6744    3.4427 H   0  0  0  0  0  0  0  0  0  0  0  0
 45 44  1  0
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 50112  1  0
 48111  1  0
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 39103  1  0
 40104  1  0
 42105  1  0
M  END


  Mrv1652304292202422D          

 50 51  0  0  0  0            999 V2000
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   18.5762    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   22.1486   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.7223   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.4367   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.1512   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.8657   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.5801   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.2946   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.0091   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.7235   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   36.4380   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   36.4380   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   37.1525   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8670   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8670   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.5814   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   38.5814   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8670   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.1525   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.1525   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   37.8670   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   39.2959   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   39.2959   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
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 14 15  1  0  0  0  0
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 16 17  1  0  0  0  0
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 20 21  1  0  0  0  0
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 29 30  1  0  0  0  0
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 31 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
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
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 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
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 39 44  1  0  0  0  0
 42 45  1  0  0  0  0
 41 46  1  0  0  0  0
 46 47  1  0  0  0  0
  3 48  1  0  0  0  0
 48 49  1  0  0  0  0
  2 50  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0079700

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(\C=C\C(=O)OCCCCCCCCCCCCCCCCCCCCCCOC(=O)\C=C/C2=CC(OC)=C(O)C=C2)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C42H62O8/c1-47-39-33-35(23-27-37(39)43)25-29-41(45)49-31-21-19-17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-20-22-32-50-42(46)30-26-36-24-28-38(44)40(34-36)48-2/h23-30,33-34,43-44H,3-22,31-32H2,1-2H3/b29-25-,30-26+

> <INCHI_KEY>
FKPYDKGDBYFMGX-ZUSIYWPSSA-N

> <FORMULA>
C42H62O8

> <MOLECULAR_WEIGHT>
694.95

> <EXACT_MASS>
694.444468956

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
84.69783783560808

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
22-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}docosyl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
9.16

> <JCHEM_LOGP>
12.516187560666669

> <ALOGPS_LOGS>
-7.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.16883689042575

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.566776899097789

> <JCHEM_PKA_STRONGEST_BASIC>
-4.587682067289761

> <JCHEM_POLAR_SURFACE_AREA>
111.52000000000001

> <JCHEM_REFRACTIVITY>
202.9052

> <JCHEM_ROTATABLE_BOND_COUNT>
31

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.88e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
22-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}docosyl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0      29.341  -4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      28.007  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      28.007  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      29.341  -1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      30.675  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      30.675  -3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      32.008  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      33.342  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      34.676  -1.540   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      34.676   0.000   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      36.009  -2.310   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      37.343  -1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      38.677  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      40.010  -1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      41.344  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      42.678  -1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      44.011  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      45.345  -1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      46.679  -2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      48.012  -1.540   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      49.346  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      50.680  -1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      52.013  -2.310   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      53.347  -1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      54.681  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      56.015  -1.540   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      57.348  -2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      58.682  -1.540   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      60.016  -2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      61.349  -1.540   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      62.683  -2.310   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      64.017  -1.540   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      65.350  -2.310   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      66.684  -1.540   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      68.018  -2.310   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      68.018  -3.850   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      69.351  -1.540   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      70.685  -2.310   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      70.685  -3.850   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      72.019  -4.620   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      72.019  -6.160   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      70.685  -6.930   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      69.351  -6.160   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      69.351  -4.620   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      70.685  -8.470   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      73.352  -6.930   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      73.352  -8.470   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      26.674  -1.540   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      25.340  -2.310   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0      26.674  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   50                                                  
CONECT    3    2    4   48                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
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                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   44                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   46                                                  
CONECT   42   41   43   45                                                  
CONECT   43   42   44                                                       
CONECT   44   43   39                                                       
CONECT   45   42                                                            
CONECT   46   41   47                                                       
CONECT   47   46                                                            
CONECT   48    3   49                                                       
CONECT   49   48                                                            
CONECT   50    2                                                            
MASTER        0    0    0    0    0    0    0    0   50    0  102    0
END

View in JSmol

Synonyms

Value	Source
22-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}docosyl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₄₂H₆₂O₈

Average Mass

694.9500 Da

Monoisotopic Mass

694.44447 Da

IUPAC Name

22-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}docosyl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

Traditional Name

22-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy}docosyl (2Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

COC1=CC(\C=C\C(=O)OCCCCCCCCCCCCCCCCCCCCCCOC(=O)\C=C/C2=CC(OC)=C(O)C=C2)=CC=C1O

InChI Identifier

InChI=1S/C42H62O8/c1-47-39-33-35(23-27-37(39)43)25-29-41(45)49-31-21-19-17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-20-22-32-50-42(46)30-26-36-24-28-38(44)40(34-36)48-2/h23-30,33-34,43-44H,3-22,31-32H2,1-2H3/b29-25-,30-26+

InChI Key

FKPYDKGDBYFMGX-ZUSIYWPSSA-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
Garcinia multiflora	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acids and derivatives. These are aromatic compounds containing Aromatic compounds containing a cinnamic acid moiety (or a derivative thereof) hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acids and derivatives

Alternative Parents

Substituents

Coumaric acid or derivatives
Fatty alcohol ester
Cinnamic acid ester
Methoxyphenol
Anisole
Phenoxy compound
Phenol ether
Styrene
Methoxybenzene
Phenol
1-hydroxy-2-unsubstituted benzenoid
Fatty acid ester
Alkyl aryl ether
Fatty acyl
Monocyclic benzene moiety
Benzenoid
Dicarboxylic acid or derivatives
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Carboxylic acid derivative
Ether
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	9.16	ALOGPS
logP	12.52	ChemAxon
logS	-7.4	ALOGPS
pKa (Strongest Acidic)	9.57	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	111.52 Å²	ChemAxon
Rotatable Bond Count	31	ChemAxon
Refractivity	202.91 m³·mol⁻¹	ChemAxon
Polarizability	84.7 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00044401

Chemspider ID

9214932

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11039760

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (1E,22Z)-1,22-Diferuloyloxydocosane (NP0079700)

MOL for NP0079700 ((1E,22Z)-1,22-Diferuloyloxydocosane)

3D MOL for NP0079700 ((1E,22Z)-1,22-Diferuloyloxydocosane)

3D SDF for NP0079700 ((1E,22Z)-1,22-Diferuloyloxydocosane)

3D-SDF for NP0079700 ((1E,22Z)-1,22-Diferuloyloxydocosane)

PDB for NP0079700 ((1E,22Z)-1,22-Diferuloyloxydocosane)

3D PDB for NP0079700 ((1E,22Z)-1,22-Diferuloyloxydocosane)

SMILES for NP0079700 ((1E,22Z)-1,22-Diferuloyloxydocosane)

INCHI for NP0079700 ((1E,22Z)-1,22-Diferuloyloxydocosane)

Structure for NP0079700 ((1E,22Z)-1,22-Diferuloyloxydocosane)

3D Structure for NP0079700 ((1E,22Z)-1,22-Diferuloyloxydocosane)