NP-MRD: Showing NP-Card for methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate (NP0253778)

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Record Information

Version

2.0

Created at

2022-09-07 17:45:03 UTC

Updated at

2022-09-07 17:45:03 UTC

NP-MRD ID

NP0253778

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate

Description

Lipidyl Pseudopterane C belongs to the class of organic compounds known as furoic acid esters. These are ester derivatives of furoic acid. methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate is found in Antillogorgia acerosa. Based on a literature review very few articles have been published on Lipidyl Pseudopterane C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072219452D          

 47 49  0  0  1  0            999 V2000
   -0.9350   -5.5200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8237   -4.7026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0601   -4.3902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4760   -4.1974    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7309   -4.9820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559   -4.9820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8108   -4.1974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8434   -4.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3277   -5.2734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5457   -6.0691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9656   -6.6557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3438   -6.2782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5617   -7.0739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7779   -1.6904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3285   -0.9986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6029   -1.6904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0088   -4.1094    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
  4  2  1  6  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  2  0  0  0  0
  9 10  1  0  0  0  0
  6 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  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
 19 24  1  6  0  0  0
 21 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 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  1  0  0  0  0
 36 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  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 25 46  1  0  0  0  0
  4 46  1  0  0  0  0
 46 47  1  6  0  0  0
M  END

     RDKit          3D

105107  0  0  0  0  0  0  0  0999 V2000
   -3.3488   -1.1675    2.6668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2618   -0.5892    1.8579 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0921    0.8580    1.7982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2897   -1.4260    1.1554 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.7070   -1.1118    1.4359 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3971   -0.0978    0.5879 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7198    0.7143   -0.1013 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4527    1.5324   -0.7876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7371    1.2298   -0.5226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7335    0.1759    0.3664 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8870   -0.4918    0.9336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8052   -1.4461    1.7446 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1540   -0.0681    0.5722 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3623   -0.6045    1.0254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6322    2.5159   -1.6295 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.3754    2.7747   -2.8621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7260    4.0548   -3.0873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7752    1.7675   -3.8783 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3853    1.7997   -1.8303 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.6530    0.2844   -2.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4730   -0.1893   -1.8209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5552    0.8632   -2.3719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3049    0.8794   -2.4508 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4596    1.9037   -2.8198 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0628   -1.4403   -1.1616 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7103   -1.3943   -0.7561 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6866   -2.1420   -1.2817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9930   -2.9380   -2.2035 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2700   -2.0555   -0.8228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1335   -0.9885    0.2270 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3360   -0.8570    0.7114 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7811   -2.1278    1.3020 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0935   -2.2413    1.9283 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3465   -2.0471    1.1842 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6737   -0.7291    0.6169 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0267   -0.7156   -0.0934 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1510   -1.0617    0.8269 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2399   -0.0854    1.9837 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4503    1.3134    1.5032 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7174    1.4854    0.6878 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9446    1.1356    1.4589 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1677    1.3304    0.6117 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1937    0.4803   -0.6317 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4987    0.7651   -1.3981 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5246    2.2221   -1.7604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8923   -2.0192   -0.1135 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.1223   -2.4116   -0.7413 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5852   -0.6403    3.2020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4062   -2.2589    2.7711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9703    1.4836    1.7496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5115    1.2489    2.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4037    1.1135    0.9400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1972   -2.3670    1.8777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3057   -2.0779    1.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8890   -0.7312    2.4788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6069    1.7548   -0.9586 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1578   -0.2022    0.3308 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4156   -1.7182    0.8650 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6628   -0.3204    2.0322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4350    3.4225   -1.0287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4719    4.8621   -2.3902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2753    4.2602   -3.9935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3828    2.2335   -4.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4705    1.0558   -3.3878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9368    1.1881   -4.2910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8373    1.8297   -0.8150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6858    0.0318   -2.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9940   -2.2090   -1.9834 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4131   -1.8435   -1.6873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0215   -3.0774   -0.4623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7409   -1.2625    1.0980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3962   -0.0204   -0.2080 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9013   -0.6059   -0.2182 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3361   -0.0533    1.4611 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9851   -2.5426    2.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7681   -2.9082    0.4460 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1218   -3.2342    2.5052 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1238   -1.5210    2.8513 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2003   -2.4130    1.8733 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4079   -2.8345    0.3584 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9335   -0.3716   -0.1040 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7308    0.0073    1.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0116   -1.4384   -0.9480 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2001    0.2985   -0.5040 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0211   -2.0990    1.1851 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1149   -0.9831    0.2538 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0887   -0.3969    2.6563 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3514   -0.1107    2.6319 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5868    1.9524    2.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6072    1.6751    0.9185 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6809    0.9079   -0.2398 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7766    2.5761    0.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9556    0.0659    1.7911 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0408    1.8159    2.3469 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.1100    1.1948    1.1800 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1492    2.3933    0.2670 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3303    0.6822   -1.3180 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.2424   -0.5812   -0.3265 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3297    0.4762   -0.6993 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5017    0.1168   -2.2905 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.1798    2.7540   -1.0228 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9534    2.4000   -2.7758 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5175    2.6840   -1.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4527   -3.0430    0.1105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4889   -3.2212   -0.3288 H   0  0  0  0  0  0  0  0  0  0  0  0
 45 44  1  0
 44 43  1  0
 43 42  1  0
 42 41  1  0
 41 40  1  0
 40 39  1  0
 39 38  1  0
 38 37  1  0
 37 36  1  0
 36 35  1  0
 35 34  1  0
 34 33  1  0
 33 32  1  0
 32 31  1  0
 31 30  1  0
 30 29  1  0
 29 27  1  0
 27 28  2  0
 27 26  1  0
 26 25  1  0
 25 46  1  0
 46 47  1  0
 46  4  1  0
  4  5  1  0
  5  6  1  0
  6 10  2  0
 10  9  1  0
  9  8  2  0
  8  7  1  0
  8 15  1  0
 15 19  1  0
 19 24  1  0
 24 22  1  0
 22 23  2  0
 22 21  1  0
 21 20  2  0
 15 16  1  0
 16 18  1  0
 16 17  2  3
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  1  0
  4  2  1  0
  2  3  1  0
  2  1  2  3
 21 25  1  0
  7  6  1  0
 20 19  1  0
 45101  1  0
 45102  1  0
 45103  1  0
 44 99  1  0
 44100  1  0
 43 97  1  0
 43 98  1  0
 42 95  1  0
 42 96  1  0
 41 93  1  0
 41 94  1  0
 40 91  1  0
 40 92  1  0
 39 89  1  0
 39 90  1  0
 38 87  1  0
 38 88  1  0
 37 85  1  0
 37 86  1  0
 36 83  1  0
 36 84  1  0
 35 81  1  0
 35 82  1  0
 34 79  1  0
 34 80  1  0
 33 77  1  0
 33 78  1  0
 32 75  1  0
 32 76  1  0
 31 73  1  0
 31 74  1  0
 30 71  1  0
 30 72  1  0
 29 69  1  0
 29 70  1  0
 25 68  1  6
 46104  1  1
 47105  1  0
  4 53  1  1
  5 54  1  0
  5 55  1  0
  9 56  1  0
 15 60  1  1
 19 66  1  1
 20 67  1  0
 18 63  1  0
 18 64  1  0
 18 65  1  0
 17 61  1  0
 17 62  1  0
 14 57  1  0
 14 58  1  0
 14 59  1  0
  3 50  1  0
  3 51  1  0
  3 52  1  0
  1 48  1  0
  1 49  1  0
M  END


  Mrv1652309072219452D          

 47 49  0  0  1  0            999 V2000
   -0.9350   -5.5200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8237   -4.7026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0601   -4.3902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4760   -4.1974    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7309   -4.9820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559   -4.9820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8108   -4.1974    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8434   -4.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3277   -5.2734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5457   -6.0691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9656   -6.6557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3438   -6.2782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5617   -7.0739    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7779   -1.6904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3285   -0.9986    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6029   -1.6904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0088   -4.1094    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
  4  2  1  6  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  2  0  0  0  0
  9 10  1  0  0  0  0
  6 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
  8 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  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
 19 24  1  6  0  0  0
 21 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 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  1  0  0  0  0
 36 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  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 25 46  1  0  0  0  0
  4 46  1  0  0  0  0
 46 47  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0253778

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCC(=O)O[C@H]1[C@H](O)[C@H](CC2=C(C=C(O2)[C@@H]([C@@H]2OC(=O)C1=C2)C(C)=C)C(=O)OC)C(C)=C

> <INCHI_IDENTIFIER>
InChI=1S/C39H58O8/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-34(40)47-37-30-25-33(46-39(30)43)35(27(4)5)32-24-29(38(42)44-6)31(45-32)23-28(26(2)3)36(37)41/h24-25,28,33,35-37,41H,2,4,7-23H2,1,3,5-6H3/t28-,33-,35+,36-,37-/m1/s1

> <INCHI_KEY>
YVVIDKGYYJHJSZ-GJMMFDPESA-N

> <FORMULA>
C39H58O8

> <MOLECULAR_WEIGHT>
654.885

> <EXACT_MASS>
654.413168828

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
105

> <JCHEM_AVERAGE_POLARIZABILITY>
78.21987837809397

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2R,3R,7R,8R,9R)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1^{3,6}]pentadeca-1(13),6(15),11-triene-12-carboxylate

> <JCHEM_LOGP>
9.659672937333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.790999309620446

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.572986027129943

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0456083732405705

> <JCHEM_POLAR_SURFACE_AREA>
112.27

> <JCHEM_REFRACTIVITY>
184.054

> <JCHEM_ROTATABLE_BOND_COUNT>
22

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2R,3R,7R,8R,9R)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1^{3,6}]pentadeca-1(13),6(15),11-triene-12-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.745 -10.304   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.538  -8.778   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.112  -8.195   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.755  -7.835   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.231  -9.300   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -4.771  -9.300   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -5.247  -7.835   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -7.174  -8.642   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.212  -9.844   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.619 -11.329   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -5.536 -12.424   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      -8.108 -11.719   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -8.515 -13.205   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.319  -3.155   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.480  -1.864   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -4.859  -3.155   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      17.338  -5.390   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      20.005  -5.390   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      21.339  -4.620   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      22.673  -5.390   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      24.006  -4.620   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       0.016  -7.671   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   46                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   15                                                  
CONECT    9    8   10                                                       
CONECT   10    9    6   11                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13                                                            
CONECT   15    8   16   19                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   15   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   25                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   19                                                       
CONECT   25   21   26   46                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   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                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44                                                            
CONECT   46   25    4   47                                                  
CONECT   47   46                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₅₈O₈

Average Mass

654.8850 Da

Monoisotopic Mass

654.41317 Da

IUPAC Name

methyl (2R,3R,7R,8R,9R)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1^{3,6}]pentadeca-1(13),6(15),11-triene-12-carboxylate

Traditional Name

methyl (2R,3R,7R,8R,9R)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1^{3,6}]pentadeca-1(13),6(15),11-triene-12-carboxylate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCC(=O)O[C@H]1[C@H](O)[C@H](CC2=C(C=C(O2)[C@@H]([C@@H]2OC(=O)C1=C2)C(C)=C)C(=O)OC)C(C)=C

InChI Identifier

InChI=1S/C39H58O8/c1-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-34(40)47-37-30-25-33(46-39(30)43)35(27(4)5)32-24-29(38(42)44-6)31(45-32)23-28(26(2)3)36(37)41/h24-25,28,33,35-37,41H,2,4,7-23H2,1,3,5-6H3/t28-,33-,35+,36-,37-/m1/s1

InChI Key

YVVIDKGYYJHJSZ-GJMMFDPESA-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
Antillogorgia acerosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furoic acid esters. These are ester derivatives of furoic acid.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Furans

Sub Class

Furoic acid and derivatives

Direct Parent

Furoic acid esters

Alternative Parents

Substituents

Furoic acid ester
Furan-3-carboxylic acid ester
Furan-3-carboxylic acid or derivatives
Fatty acid ester
2-furanone
Dicarboxylic acid or derivatives
Fatty acyl
Dihydrofuran
Methyl ester
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Heteroaromatic compound
Secondary alcohol
Lactone
Carboxylic acid ester
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Alcohol
Organic oxide
Organic oxygen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	9.66	ChemAxon
pKa (Strongest Acidic)	12.57	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	112.27 Å²	ChemAxon
Rotatable Bond Count	22	ChemAxon
Refractivity	184.05 m³·mol⁻¹	ChemAxon
Polarizability	78.22 Å³	ChemAxon
Number of Rings	3	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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

27023887

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

102279560

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate (NP0253778)

MOL for NP0253778 (methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate)

3D MOL for NP0253778 (methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate)

3D SDF for NP0253778 (methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate)

3D-SDF for NP0253778 (methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate)

PDB for NP0253778 (methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate)

3D PDB for NP0253778 (methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate)

SMILES for NP0253778 (methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate)

INCHI for NP0253778 (methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate)

Structure for NP0253778 (methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate)

3D Structure for NP0253778 (methyl (2r,3r,7r,8r,9r)-8-hydroxy-7-(octadecanoyloxy)-5-oxo-2,9-bis(prop-1-en-2-yl)-4,14-dioxatricyclo[9.2.1.1³,⁶]pentadeca-1(13),6(15),11-triene-12-carboxylate)