NP-MRD: Showing NP-Card for methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate (NP0316142)

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Record Information

Version

2.0

Created at

2022-09-11 15:08:20 UTC

Updated at

2022-09-11 15:08:20 UTC

NP-MRD ID

NP0316142

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate

Description

Methyl (1S,4aR,6S,7R,7aS)-6-{[(2E)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2S,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton. methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate is found in Duranta erecta. Based on a literature review very few articles have been published on methyl (1S,4aR,6S,7R,7aS)-6-{[(2E)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2S,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112217082D          

 55 58  0  0  1  0            999 V2000
    3.9934    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1368   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1368   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5658   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7079   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2789   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4782    1.6455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4699    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0574    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7676    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0051    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4176    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2426    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6551    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4801    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8926    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4801    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7176    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2426    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4176    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9429   -1.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1726   -0.8134    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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 23 28  1  0  0  0  0
 10 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
  8 33  1  0  0  0  0
 33 34  1  6  0  0  0
  5 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 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
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
 46 51  1  0  0  0  0
 51 52  2  0  0  0  0
 43 52  1  0  0  0  0
 37 53  1  0  0  0  0
 33 53  1  0  0  0  0
 53 54  1  6  0  0  0
 53 55  1  1  0  0  0
M  END

     RDKit          3D

 97100  0  0  0  0  0  0  0  0999 V2000
    1.9526    3.3792    6.8379 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0316    3.0524    5.8061 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3994    3.1126    4.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5798    3.4703    4.2489 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4524    2.7767    3.4257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7878    2.4108    3.8191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6951    2.0885    2.8486 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2764    1.2097    1.8011 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2142    1.2472    0.7466 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8601    0.0251    0.5962 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4696   -0.5004   -0.6201 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4855   -1.1904   -1.2626 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8961   -1.8362   -2.4829 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8555   -2.5674   -3.1951 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5605   -3.6348   -2.7022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5825   -4.3900   -3.5040 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3661   -4.0223   -1.5341 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4855   -0.1596   -1.7266 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4662   -0.7295   -2.5759 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6153   -0.3633   -3.9037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6600   -0.9810   -4.7806 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8637    0.5100   -4.4086 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0859    0.4556   -0.5078 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2350    1.8539   -0.8056 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5209    2.3448   -0.8905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8092    3.7704   -1.1916 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4830    1.5626   -0.7075 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3298    0.2257    0.7385 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8570   -0.8905    1.4384 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4670   -0.8287    2.6649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9641   -2.1085    3.2528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5725    0.2816    3.2169 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0508    1.6006    1.2541 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6832    2.7962    1.9728 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1541    3.9869    1.4774 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1373    2.6149    1.5703 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3458    1.1619    1.8901 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.4570    0.5821    1.2563 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4657   -0.0746    1.9263 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3793   -0.1568    3.1775 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6103   -0.6635    1.2101 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6362   -0.5388   -0.1010 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7193   -1.0848   -0.8823 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7832   -1.7566   -0.3658 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7963   -2.2556   -1.1920 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7479   -2.0819   -2.5580 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7493   -2.5741   -3.3855 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8869   -1.8182   -3.7102 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9177   -2.3900   -4.5917 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0032   -0.6607   -3.2384 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6859   -1.4110   -3.0783 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6839   -0.9172   -2.2627 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0944    0.5299    1.3095 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7234   -0.6709    2.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4110    0.1010    0.0064 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9012    2.6472    7.6765 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7481    4.3753    7.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0117    3.3739    6.4490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0215    2.3859    4.8951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2903    0.1774    2.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4474   -0.6452    1.3767 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9941   -1.9172   -0.6350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9927   -2.4223   -2.2343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5482   -1.0215   -3.1819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5822   -3.9585   -3.3842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6566   -5.4441   -3.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2524   -4.4984   -4.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8874    0.6035   -2.3043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4624   -1.4540   -4.1780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0613   -0.1867   -5.4404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1721   -1.7359   -5.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0960   -0.0345   -0.3839 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8120    4.0753   -0.8439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0738    4.4305   -0.6867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7941    3.8835   -2.2970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5345    1.1082    1.4179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0704   -2.6909    3.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6582   -1.9445    4.0800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4177   -2.6679    2.3982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0430    1.9525    0.1847 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6217    4.2769    1.9931 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7875    3.3250    2.0430 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1361    2.7480    0.4539 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3806    1.0295    2.9937 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3777   -1.1668    1.7460 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8203   -0.0089   -0.6268 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8737   -1.9223    0.6977 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6289   -2.7844   -0.7563 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5106   -2.9776   -5.4338 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6121   -3.0133   -3.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5390   -1.5417   -4.9820 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6158   -1.2551   -4.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8585   -0.3908   -2.7177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5010   -0.4422    3.1744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0435   -1.3028    1.6266 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6489   -1.3190    2.1483 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5081   -0.8814   -0.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 12 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 18 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  2  0
 23 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
  8 33  1  0
 33 53  1  0
 53 54  1  0
 53 55  1  6
 53 37  1  0
 37 36  1  0
 36 34  1  0
 34 35  1  6
 37 38  1  0
 38 39  1  0
 39 40  2  0
 39 41  1  0
 41 42  2  0
 42 43  1  0
 43 44  2  0
 44 45  1  0
 45 46  2  0
 46 47  1  0
 47 48  1  0
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 48 50  2  0
 46 51  1  0
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 34  5  1  0
 52 43  1  0
 28 10  1  0
 34 33  1  0
  1 56  1  0
  1 57  1  0
  1 58  1  0
  6 59  1  0
  8 60  1  1
 10 61  1  1
 12 62  1  1
 13 63  1  0
 13 64  1  0
 16 65  1  0
 16 66  1  0
 16 67  1  0
 18 68  1  6
 21 69  1  0
 21 70  1  0
 21 71  1  0
 23 72  1  1
 26 73  1  0
 26 74  1  0
 26 75  1  0
 28 76  1  1
 31 77  1  0
 31 78  1  0
 31 79  1  0
 33 80  1  6
 54 94  1  0
 54 95  1  0
 54 96  1  0
 55 97  1  0
 37 84  1  1
 36 82  1  0
 36 83  1  0
 35 81  1  0
 41 85  1  0
 42 86  1  0
 44 87  1  0
 45 88  1  0
 49 89  1  0
 49 90  1  0
 49 91  1  0
 51 92  1  0
 52 93  1  0
M  END


  Mrv1652309112217082D          

 55 58  0  0  1  0            999 V2000
    3.9934    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2789   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7079   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1368   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1368   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8513   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5658   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079   -2.8875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7079   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1368   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4223   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -2.4750    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2789   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4782    1.6455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4699    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0574    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7676    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1801    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0051    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4176    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2426    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6551    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4801    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8926    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4801    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7176    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2426    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4176    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9429   -1.0637    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1726   -0.8134    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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
 10  9  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 23 28  1  0  0  0  0
 10 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
  8 33  1  0  0  0  0
 33 34  1  6  0  0  0
  5 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  1  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 39 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
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 48 50  2  0  0  0  0
 46 51  1  0  0  0  0
 51 52  2  0  0  0  0
 43 52  1  0  0  0  0
 37 53  1  0  0  0  0
 33 53  1  0  0  0  0
 53 54  1  6  0  0  0
 53 55  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0316142

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]2OC(C)=O)[C@@H]2[C@@](C)(O)[C@H](C[C@]12O)OC(=O)\C=C\C1=CC=C(OC(C)=O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C36H42O19/c1-17(37)47-16-25-28(50-19(3)39)29(51-20(4)40)30(52-21(5)41)33(53-25)55-34-31-35(6,44)26(14-36(31,45)24(15-48-34)32(43)46-7)54-27(42)13-10-22-8-11-23(12-9-22)49-18(2)38/h8-13,15,25-26,28-31,33-34,44-45H,14,16H2,1-7H3/b13-10+/t25-,26+,28-,29+,30-,31-,33+,34+,35+,36+/m1/s1

> <INCHI_KEY>
CAEQIFHUCPMGKE-BGYGKCIRSA-N

> <FORMULA>
C36H42O19

> <MOLECULAR_WEIGHT>
778.713

> <EXACT_MASS>
778.232029132

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
76.06582027472558

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (1S,4aR,6S,7R,7aS)-6-{[(2E)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2S,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1H,4aH,5H,6H,7H,7aH-cyclopenta[c]pyran-4-carboxylate

> <JCHEM_LOGP>
0.3115153269999976

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.835013186733576

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.087771470271974

> <JCHEM_PKA_STRONGEST_BASIC>
-3.437033935428884

> <JCHEM_POLAR_SURFACE_AREA>
252.24999999999997

> <JCHEM_REFRACTIVITY>
177.27829999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl (1S,4aR,6S,7R,7aS)-6-{[(2E)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2S,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1H,5H,6H,7aH-cyclopenta[c]pyran-4-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       7.454   6.160   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.454   4.620   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.787   4.620   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       7.454   0.000   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       6.121  -2.310   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.454  -3.080   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.788  -2.310   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.122  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.455  -2.310   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.455  -0.770   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      10.122  -0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.122   1.540   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.788  -0.770   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.122  -4.620   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      11.455  -5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      12.789  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.789  -3.080   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      14.123  -5.390   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.788  -5.390   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.788  -6.930   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      10.122  -7.700   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.455  -6.930   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.122  -9.240   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       7.454  -4.620   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.121  -5.390   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.121  -6.930   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       7.454  -7.700   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       4.787  -7.700   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       4.626   3.072   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       0.877   0.770   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       0.107   2.104   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       0.877   3.437   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -1.433   2.104   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -2.203   3.437   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -3.743   3.437   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      -4.513   2.104   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -6.053   2.104   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      -6.823   3.437   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      -8.363   3.437   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      -9.133   2.104   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      -8.363   0.770   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0     -10.673   2.104   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      -6.053   4.771   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      -4.513   4.771   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       3.627  -1.986   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       2.189  -1.518   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   34                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   33                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   28                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18   12   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24   28                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   23   10   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33    8   34   53                                                  
CONECT   34   33    5   35   36                                             
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38   53                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   52                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47   51                                                  
CONECT   47   46   48                                                       
CONECT   48   47   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48                                                            
CONECT   51   46   52                                                       
CONECT   52   51   43                                                       
CONECT   53   37   33   54   55                                             
CONECT   54   53                                                            
CONECT   55   53                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  116    0
END

View in JSmol

Synonyms

Value	Source
Methyl (1S,4ar,6S,7R,7as)-6-{[(2E)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2S,3R,4S,5R,6R)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1H,4ah,5H,6H,7H,7ah-cyclopenta[c]pyran-4-carboxylic acid	Generator

Chemical Formula

C₃₆H₄₂O₁₉

Average Mass

778.7130 Da

Monoisotopic Mass

778.23203 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](COC(C)=O)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]2OC(C)=O)[C@@H]2[C@@](C)(O)[C@H](C[C@]12O)OC(=O)\C=C\C1=CC=C(OC(C)=O)C=C1

InChI Identifier

InChI=1S/C36H42O19/c1-17(37)47-16-25-28(50-19(3)39)29(51-20(4)40)30(52-21(5)41)33(53-25)55-34-31-35(6,44)26(14-36(31,45)24(15-48-34)32(43)46-7)54-27(42)13-10-22-8-11-23(12-9-22)49-18(2)38/h8-13,15,25-26,28-31,33-34,44-45H,14,16H2,1-7H3/b13-10+/t25-,26+,28-,29+,30-,31-,33+,34+,35+,36+/m1/s1

InChI Key

CAEQIFHUCPMGKE-BGYGKCIRSA-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
Duranta erecta	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as iridoid o-glycosides. These are iridoid monoterpenes containing a glycosyl (usually a pyranosyl) moiety linked to the iridoid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene glycosides

Direct Parent

Iridoid O-glycosides

Alternative Parents

Substituents

Iridoid o-glycoside
Cinnamic acid or derivatives
Hexose monosaccharide
Cinnamic acid ester
Glycosyl compound
Iridoid-skeleton
O-glycosyl compound
Aromatic monoterpenoid
Bicyclic monoterpenoid
Monoterpenoid
Phenol ester
Phenoxy compound
Styrene
Fatty acid ester
Monocyclic benzene moiety
Fatty acyl
Monosaccharide
Benzenoid
Oxane
Alpha,beta-unsaturated carboxylic ester
Tertiary alcohol
Methyl ester
Vinylogous ester
Enoate ester
Cyclic alcohol
Carboxylic acid ester
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Organic oxygen compound
Carbonyl group
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Alcohol
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

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

8875755

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10700414

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate (NP0316142)

MOL for NP0316142 (methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate)

3D MOL for NP0316142 (methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate)

3D SDF for NP0316142 (methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate)

3D-SDF for NP0316142 (methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate)

PDB for NP0316142 (methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate)

3D PDB for NP0316142 (methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate)

SMILES for NP0316142 (methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate)

INCHI for NP0316142 (methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate)

Structure for NP0316142 (methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate)

3D Structure for NP0316142 (methyl (1s,4ar,6s,7r,7as)-6-{[(2e)-3-[4-(acetyloxy)phenyl]prop-2-enoyl]oxy}-4a,7-dihydroxy-7-methyl-1-{[(2s,3r,4s,5r,6r)-3,4,5-tris(acetyloxy)-6-[(acetyloxy)methyl]oxan-2-yl]oxy}-1h,5h,6h,7ah-cyclopenta[c]pyran-4-carboxylate)