NP-MRD: Showing NP-Card for methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate (NP0211624)

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Record Information

Version

2.0

Created at

2022-09-05 09:59:29 UTC

Updated at

2022-09-05 09:59:30 UTC

NP-MRD ID

NP0211624

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate

Description

Methyl 2-[(1R,2S,3S,4S,6S,7R,8S,10R,12R,13R,15R,16R)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]Octadecan-6-yl]acetate belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid. Based on a literature review very few articles have been published on methyl 2-[(1R,2S,3S,4S,6S,7R,8S,10R,12R,13R,15R,16R)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]Octadecan-6-yl]acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052211592D          

 55 61  0  0  1  0            999 V2000
    4.4814    6.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4991    5.6559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9195    4.9752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2319    5.4949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0239    4.0484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9344    3.0325    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0424    2.0712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8256    2.8293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6293    2.3624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7332    1.7148    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4337    1.9324    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255    2.6357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4136    3.3628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6663    2.8502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6297    1.7771    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0803    0.9265    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2537   -0.0916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4457   -1.0271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1767   -1.4938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484   -1.5890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8876    0.9850    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6127    0.2908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3191   -0.3555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1522   -0.5923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5429   -1.2182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6845    1.2753    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6384    1.1297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5292    1.3783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0843    2.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3126    0.9778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532    0.9505    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9163    0.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9182   -0.7798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1328   -0.8610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2563   -1.7522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0139   -2.6394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5487    0.9221    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0870    0.1366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6442    0.7267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2146    0.8744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6256   -0.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2647   -0.6904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9660   -1.4595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1423   -1.4130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0680   -0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491    1.6543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5639    2.3912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8414    2.9835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0118    3.3241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7882    3.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3147    4.1277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4079    2.3953    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2070    3.1442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1143    2.4461    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6248    3.3962    0.0000 C   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
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 10 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
  7 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 15 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 31 37  1  0  0  0  0
 37 38  1  1  0  0  0
 37 39  1  6  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 41 45  2  0  0  0  0
 37 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  1  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  2  0  0  0  0
 47 52  1  0  0  0  0
 15 52  1  0  0  0  0
 52 53  1  1  0  0  0
 12 53  1  0  0  0  0
 52 54  1  0  0  0  0
  6 54  1  0  0  0  0
 10 54  1  0  0  0  0
 54 55  1  1  0  0  0
M  END

     RDKit          2D

101107  0  0  0  0  0  0  0  0999 V2000
   -8.0377    1.8541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6111    1.3906    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4964    2.3943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8082    3.8615    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0698    1.9307    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6432    1.4672    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3313    2.9344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3350    4.0492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8395    3.0912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2294    1.7209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1401    2.6151    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943    1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8578    2.6401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2760    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3943   -1.2135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1775    0.2228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8998    0.3521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0818   -0.5714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4726   -0.0095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8730   -2.0568    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1971    1.2574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3119    2.2611    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7385    1.7976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8532    2.8013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0503    0.3303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1570    2.2835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8646    3.1506    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0584    4.6380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4434    5.2139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8671    5.5495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7062   -2.6807    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5010   -3.9528    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2959   -5.2249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7950   -5.1725    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.3866   -7.8214    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4086   -3.6844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7735   -4.6079    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1128   -5.0089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4789   -6.3683    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6118   -5.0612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5353   -3.8792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9449   -4.3922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8925   -5.8913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4506   -6.3048    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8351   -3.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1470   -1.7537    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9419   -0.4816    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4410   -0.5340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2358    0.7381    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1452   -1.8584    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323   -0.7500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0323    0.7500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3442    0.7172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5577   -0.1645    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4642    2.3176    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5012    0.4275    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5741    3.2807    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1484    3.4287    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8647    0.6587    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8253    0.5439    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3387    5.1639    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2203    5.0529    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5638    3.1888    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4325    3.8862    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1514    4.5585    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4918    3.9996    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3542    2.5356    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1840    3.7192    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4530   -1.3755    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8634    0.5524    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0345   -1.4003    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9107    1.3813    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9679    3.8050    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8569    1.6865    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7211    3.7853    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2300    4.0537    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8284    5.7899    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8675    6.5990    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8462    3.7690    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1551   -2.2926    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7731   -3.1579    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.6969   -5.7900    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4831   -2.3801    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1884   -3.5534    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9376   -7.7143    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2534   -2.7325    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3971   -4.6117    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5959   -2.1419    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5350    1.4880    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5079   -0.0568    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3332    1.9361    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7712   -1.0461    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2849    1.1475    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9958   -1.5553    0.0000 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  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  6
 11 12  1  0
 12 13  1  1
 12 14  1  0
 15 14  1  1
 15 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  2  0
 33 35  1  0
 35 36  1  0
 31 37  1  0
 37 38  1  0
 37 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  1  0
 49 51  2  0
 47 52  1  0
 52 53  1  1
 52 54  1  0
 54 55  1  1
 37 39  1  6
 39 40  2  0
 39 41  1  0
 41 45  2  0
 45 44  1  0
 44 43  1  0
 43 42  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 16 21  1  0
 21 22  1  1
 22 23  1  0
 23 24  1  0
 23 25  2  0
 21 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  2  0
 54  6  1  0
 42 41  1  0
 26  7  1  0
 54 10  1  0
 21 10  1  0
 53 12  1  0
 52 15  1  0
  1 56  1  0
  1 57  1  0
  1 58  1  0
  5 59  1  0
  5 60  1  0
  6 61  1  6
  8 62  1  0
  8 63  1  0
  8 64  1  0
  9 65  1  0
  9 66  1  0
 13 67  1  0
 13 68  1  0
 13 69  1  0
 31 81  1  1
 32 82  1  0
 32 83  1  0
 36 84  1  0
 36 85  1  0
 36 86  1  0
 38 87  1  0
 38 88  1  0
 38 89  1  0
 46 93  1  0
 46 94  1  0
 47 95  1  6
 50 96  1  0
 50 97  1  0
 50 98  1  0
 55 99  1  0
 55100  1  0
 55101  1  0
 45 92  1  0
 43 91  1  0
 42 90  1  0
 16 70  1  6
 19 71  1  0
 19 72  1  0
 19 73  1  0
 24 74  1  0
 24 75  1  0
 24 76  1  0
 26 77  1  1
 29 78  1  0
 29 79  1  0
 29 80  1  0
M  END


  Mrv1652309052211592D          

 55 61  0  0  1  0            999 V2000
    4.4814    6.5067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4991    5.6559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9195    4.9752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2319    5.4949    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0239    4.0484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9344    3.0325    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0424    2.0712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8256    2.8293    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6293    2.3624    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7332    1.7148    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4337    1.9324    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255    2.6357    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4136    3.3628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6663    2.8502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6297    1.7771    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0803    0.9265    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2537   -0.0916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4457   -1.0271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1767   -1.4938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6484   -1.5890    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8876    0.9850    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6127    0.2908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3191   -0.3555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1522   -0.5923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5429   -1.2182    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6845    1.2753    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6384    1.1297    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5292    1.3783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0843    2.0443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3126    0.9778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3532    0.9505    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9163    0.2284    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9182   -0.7798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1328   -0.8610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2563   -1.7522    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0139   -2.6394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5487    0.9221    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0870    0.1366    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6442    0.7267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2146    0.8744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6256   -0.1687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2647   -0.6904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9660   -1.4595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1423   -1.4130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0680   -0.6152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1491    1.6543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5639    2.3912    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8414    2.9835    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0118    3.3241    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7882    3.0197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3147    4.1277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4079    2.3953    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2070    3.1442    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1143    2.4461    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6248    3.3962    0.0000 C   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
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 15 14  1  1  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 10 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
 21 26  1  0  0  0  0
  7 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 15 31  1  0  0  0  0
 31 32  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
 31 37  1  0  0  0  0
 37 38  1  1  0  0  0
 37 39  1  6  0  0  0
 39 40  2  0  0  0  0
 39 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  2  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 41 45  2  0  0  0  0
 37 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  1  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 49 51  2  0  0  0  0
 47 52  1  0  0  0  0
 15 52  1  0  0  0  0
 52 53  1  1  0  0  0
 12 53  1  0  0  0  0
 52 54  1  0  0  0  0
  6 54  1  0  0  0  0
 10 54  1  0  0  0  0
 54 55  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0211624

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@H]1C2(C)C[C@]34O[C@]5(C)O[C@]6([C@H](CC(=O)OC)[C@@](C)(C[C@@H](OC(C)=O)[C@]6(O5)[C@]13C)C(=O)C1=COC=C1)[C@H](OC(C)=O)[C@@]4(OC(C)=O)[C@H]2OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C38H46O17/c1-18(39)49-25-15-31(5,28(45)22-11-12-48-16-22)24(14-27(44)47-10)36-30(51-20(3)41)37(52-21(4)42)29(50-19(2)40)32(6)17-35(37)33(7,23(32)13-26(43)46-9)38(25,36)55-34(8,53-35)54-36/h11-12,16,23-25,29-30H,13-15,17H2,1-10H3/t23-,24+,25+,29-,30-,31+,32?,33+,34+,35-,36+,37-,38-/m0/s1

> <INCHI_KEY>
WDSUDLNQRNVFBV-MTNCESCVSA-N

> <FORMULA>
C38H46O17

> <MOLECULAR_WEIGHT>
774.769

> <EXACT_MASS>
774.273500021

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
101

> <JCHEM_AVERAGE_POLARIZABILITY>
37.01358333580652

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[(1R,2S,3S,4S,6S,7R,8S,10R,12R,13R,15R,16R)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1^{5,8}.0^{1,12}.0^{3,8}.0^{7,12}]octadecan-6-yl]acetate

> <JCHEM_LOGP>
1.585210780666667

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-2.98966398537362

> <JCHEM_POLAR_SURFACE_AREA>
215.7

> <JCHEM_REFRACTIVITY>
177.24319999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(1R,2S,3S,4S,6S,7R,8S,10R,12R,13R,15R,16R)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1^{5,8}.0^{1,12}.0^{3,8}.0^{7,12}]octadecan-6-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       8.365  12.146   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.398  10.558   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       7.316   9.287   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.033  10.257   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.511   7.557   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.344   5.661   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.546   3.866   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.008   5.281   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.641   4.410   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.969   3.201   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.276   3.607   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.954   4.920   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.239   6.277   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.977   5.320   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.909   3.317   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.750   1.729   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.074  -0.171   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.432  -1.917   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       7.797  -2.789   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.944  -2.966   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.257   1.839   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.610   0.543   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.929  -0.664   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.484  -1.106   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      10.347  -2.274   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       8.744   2.381   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.525   2.109   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      12.188   2.573   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      13.224   3.816   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      13.650   1.825   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       4.393   1.774   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.444   0.426   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.447  -1.456   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.981  -1.607   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       6.078  -3.271   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       5.626  -4.927   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.891   1.721   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       2.029   0.255   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.202   1.357   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -0.401   1.632   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       1.168  -0.315   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       2.361  -1.289   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       1.803  -2.724   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       0.266  -2.638   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0      -0.127  -1.148   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.145   3.088   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       2.919   4.464   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       1.571   5.569   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       0.022   6.205   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      -1.471   5.637   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0      -0.587   7.705   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0       4.495   4.471   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0       5.986   5.869   0.000  0.00  0.00           O+0
HETATM   54  C   UNK     0       5.813   4.566   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0       4.900   6.340   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   54                                                  
CONECT    7    6    8    9   26                                             
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   21   54                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   14   53                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   31   52                                             
CONECT   16   15   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   10   22   26                                             
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   21    7   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   15   32   37                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35                                                            
CONECT   37   31   38   39   46                                             
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   42   45                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   41                                                       
CONECT   46   37   47                                                       
CONECT   47   46   48   52                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50   51                                                  
CONECT   50   49                                                            
CONECT   51   49                                                            
CONECT   52   47   15   53   54                                             
CONECT   53   52   12                                                       
CONECT   54   52    6   10   55                                             
CONECT   55   54                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  122    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[(1R,2S,3S,4S,6S,7R,8S,10R,12R,13R,15R,16R)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1,.0,.0,.0,]octadecan-6-yl]acetic acid	Generator

Chemical Formula

C₃₈H₄₆O₁₇

Average Mass

774.7690 Da

Monoisotopic Mass

774.27350 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@H]1C2(C)C[C@]34O[C@]5(C)O[C@]6([C@H](CC(=O)OC)[C@@](C)(C[C@@H](OC(C)=O)[C@]6(O5)[C@]13C)C(=O)C1=COC=C1)[C@H](OC(C)=O)[C@@]4(OC(C)=O)[C@H]2OC(C)=O

InChI Identifier

InChI=1S/C38H46O17/c1-18(39)49-25-15-31(5,28(45)22-11-12-48-16-22)24(14-27(44)47-10)36-30(51-20(3)41)37(52-21(4)42)29(50-19(2)40)32(6)17-35(37)33(7,23(32)13-26(43)46-9)38(25,36)55-34(8,53-35)54-36/h11-12,16,23-25,29-30H,13-15,17H2,1-10H3/t23-,24+,25+,29-,30-,31+,32?,33+,34+,35-,36+,37-,38-/m0/s1

InChI Key

WDSUDLNQRNVFBV-MTNCESCVSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Prostaglandins and related compounds

Alternative Parents

Substituents

Prostaglandin skeleton
Hexacarboxylic acid or derivatives
Diterpenoid
Aryl alkyl ketone
Aryl ketone
Ortho ester
Dioxepane
Carboxylic acid orthoester
1,3-dioxepane
Meta-dioxane
Heteroaromatic compound
Methyl ester
Furan
Meta-dioxolane
Orthocarboxylic acid derivative
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163189487

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate (NP0211624)

MOL for NP0211624 (methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate)

3D MOL for NP0211624 (methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate)

3D SDF for NP0211624 (methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate)

3D-SDF for NP0211624 (methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate)

PDB for NP0211624 (methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate)

3D PDB for NP0211624 (methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate)

SMILES for NP0211624 (methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate)

INCHI for NP0211624 (methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate)

Structure for NP0211624 (methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate)

3D Structure for NP0211624 (methyl 2-[(1r,2s,3s,4s,6s,7r,8s,10r,12r,13r,15r,16r)-2,3,4,13-tetrakis(acetyloxy)-15-(furan-3-carbonyl)-16-(2-methoxy-2-oxoethyl)-5,7,10,15-tetramethyl-9,11,17-trioxahexacyclo[8.6.1.1⁵,⁸.0¹,¹².0³,⁸.0⁷,¹²]octadecan-6-yl]acetate)