NP-MRD: Showing NP-Card for methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate (NP0254915)

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Record Information

Version

2.0

Created at

2022-09-07 19:13:47 UTC

Updated at

2022-09-07 19:13:47 UTC

NP-MRD ID

NP0254915

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate

Description

Dichapetalin C belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate is found in Dichapetalum madagascariense. Based on a literature review very few articles have been published on Dichapetalin C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072221132D          

 46 52  0  0  1  0            999 V2000
    0.5169   -2.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3576   -1.6681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4230   -1.4012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0445   -1.9439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5823   -0.5917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3629   -0.3249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9843   -0.8675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8251   -1.6770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7650   -0.6007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3864   -1.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8438   -1.7648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9291   -0.5219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0078   -1.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7885   -1.4192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0391   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0346    0.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7241    1.0967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2667    0.4752    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6683   -0.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8434   -0.2329    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2450   -0.9535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0699   -0.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4932   -0.2580    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3181   -0.2705    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8948   -0.9786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7197   -0.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5446   -1.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9679   -0.2956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7928   -0.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2162    0.4000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0411    0.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4644    1.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2893    1.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6909    0.3623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2676   -0.3458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4427   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8146    1.1206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9897    1.1332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5664    0.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1648    1.1457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7414    0.4376    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3399    1.1583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5150    1.1708    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1134    1.8915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0916    0.4627    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6901    1.1833    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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 20 19  1  6  0  0  0
 15 20  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 23 22  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 30 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 28 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 24 41  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  0  0  0  0
 23 45  1  0  0  0  0
 18 45  1  0  0  0  0
 45 46  1  1  0  0  0
M  END

     RDKit          3D

 98104  0  0  0  0  0  0  0  0999 V2000
   -4.7702   -4.5373   -0.0838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7451   -3.1381   -0.0549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2391   -2.3825    0.9739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7553   -2.9432    1.9790 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2394   -0.8653    0.9564 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7379   -0.5769    0.8244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2325    0.7621    0.7925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3946    1.3477    1.8869 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6033    1.5890   -0.3893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0088    2.1736   -0.2246 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.1192    3.0486    0.9867 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2000    2.9714   -1.3541 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0501    1.0776   -0.2842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8090    0.3630   -1.4800 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5225   -0.3112   -0.1776 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4883    1.2021   -0.1128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0299    1.6078    0.0621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2706    0.4889   -0.5897 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7197    0.0382   -1.8655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1648   -0.6857   -0.5529 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4999   -1.9713   -0.2945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1664   -2.1465   -0.3024 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6528   -0.9662   -0.5902 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1148   -1.1151   -0.3788 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4624   -1.5376    1.0146 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6838   -2.1611   -1.3216 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1456   -2.2328   -0.9731 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8535   -1.1120   -0.8947 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3077   -1.1097   -0.5533 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6214    0.1769    0.1422 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0426    0.3813    0.4110 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5222    0.2492    1.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8725    0.4356    1.9929 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7688    0.7602    0.9979 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2981    0.8932   -0.2817 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9646    0.7066   -0.5609 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1913    1.2160   -0.6907 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8337    1.3600   -0.4919 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1525    0.1646   -1.1646 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3764    0.4176   -2.6682 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7156    0.1940   -0.7982 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3234    1.2326    0.2231 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8302    1.4254    0.1903 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5012    2.3165   -0.8278 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0309    0.1872    0.1014 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3394   -0.2611    1.5241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9196   -5.0101   -0.5744 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9049   -4.8785    0.9752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7444   -4.8125   -0.5861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8968   -0.4845    1.9189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9849   -1.0488   -0.1894 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3022   -1.2564    1.5284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9694    2.5047   -0.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5338    1.0306   -1.3353 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1654    3.5584    1.1627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4166    2.5033    1.9054 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8669    3.8369    0.7523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3666    3.4917   -1.5537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0187    0.4357    0.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0266    1.5765   -0.4516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0951   -0.3023   -1.3059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1675   -0.5086   -1.1194 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8085    1.6890   -1.0536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9910    1.5991    0.7903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7624    1.7781    1.1072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8023    2.5413   -0.4917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4835    0.6588   -2.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2715   -0.6760   -2.5612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0914   -2.8468   -0.0972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2242   -3.1370   -0.0987 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5534   -0.7697   -1.7013 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1965   -0.8387    1.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9492   -2.5346    1.1631 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5375   -1.7597    1.1100 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5710   -1.8893   -2.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2403   -3.1603   -1.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6571   -3.1641   -0.7809 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4365   -1.9307    0.2028 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9393   -1.3313   -1.4158 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9889    0.2215    1.0557 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8597   -0.0018    2.4998 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2653    0.3352    2.9983 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8378    0.9097    1.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9795    1.1443   -1.0685 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5725    0.8098   -1.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5337    2.2579   -1.1090 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5872    1.4591    0.5608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4087    0.8729   -3.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1997    1.1009   -2.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4576   -0.5460   -3.2089 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1636    0.5120   -1.7380 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7104    1.0434    1.2328 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7674    2.1949   -0.1093 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5660    1.9565    1.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6169    3.2659   -0.5037 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4253   -0.1477    1.7288 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1724    0.3680    2.2820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1371   -1.3540    1.6622 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  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  6
 10 13  1  0
 13 14  1  0
  5 15  1  0
 15 16  1  0
 16 17  1  0
 18 17  1  1
 18 19  1  0
 19 20  1  0
 20 21  1  6
 21 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  1  1
 24 26  1  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  1  0
 30 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  6
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 20 15  1  0
 45 23  1  0
 36 31  1  0
 20 18  1  0
 41 24  1  0
 45 18  1  0
 39 28  1  0
  1 47  1  0
  1 48  1  0
  1 49  1  0
  5 50  1  1
  6 51  1  0
  6 52  1  0
  9 53  1  0
  9 54  1  0
 11 55  1  0
 11 56  1  0
 11 57  1  0
 12 58  1  0
 13 59  1  0
 13 60  1  0
 14 61  1  0
 15 62  1  6
 16 63  1  0
 16 64  1  0
 17 65  1  0
 17 66  1  0
 19 67  1  0
 19 68  1  0
 21 69  1  0
 22 70  1  0
 23 71  1  6
 25 72  1  0
 25 73  1  0
 25 74  1  0
 26 75  1  0
 26 76  1  0
 27 77  1  0
 29 78  1  0
 29 79  1  0
 30 80  1  1
 38 86  1  0
 38 87  1  0
 40 88  1  0
 40 89  1  0
 40 90  1  0
 41 91  1  6
 42 92  1  0
 42 93  1  0
 43 94  1  1
 44 95  1  0
 46 96  1  0
 46 97  1  0
 46 98  1  0
 32 81  1  0
 33 82  1  0
 34 83  1  0
 35 84  1  0
 36 85  1  0
M  END


  Mrv1652309072221132D          

 46 52  0  0  1  0            999 V2000
    0.5169   -2.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3576   -1.6681    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4230   -1.4012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0445   -1.9439    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5823   -0.5917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3629   -0.3249    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9843   -0.8675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8251   -1.6770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7650   -0.6007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3864   -1.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8438   -1.7648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9291   -0.5219    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0078   -1.6860    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7885   -1.4192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0391   -0.0491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0346    0.7726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7241    1.0967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2667    0.4752    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6683   -0.2454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8434   -0.2329    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2450   -0.9535    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0699   -0.9661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4932   -0.2580    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3181   -0.2705    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8948   -0.9786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7197   -0.9912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5446   -1.0037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9679   -0.2956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7928   -0.3082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2162    0.4000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0411    0.3874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4644    1.0955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2893    1.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6909    0.3623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2676   -0.3458    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4427   -0.3333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8146    1.1206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9897    1.1332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5664    0.4250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1648    1.1457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7414    0.4376    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3399    1.1583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5150    1.1708    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1134    1.8915    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0916    0.4627    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6901    1.1833    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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 20 19  1  6  0  0  0
 15 20  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 23 22  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  6  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 31 36  1  0  0  0  0
 30 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 28 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 24 41  1  0  0  0  0
 41 42  1  1  0  0  0
 42 43  1  0  0  0  0
 43 44  1  6  0  0  0
 43 45  1  0  0  0  0
 23 45  1  0  0  0  0
 18 45  1  0  0  0  0
 45 46  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0254915

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(CC(=O)CC(C)(O)CO)C1CC[C@]23C[C@]12C=C[C@@H]1[C@@]2(C)CC=C4C[C@H](OC[C@]4(C)[C@@H]2C[C@@H](O)[C@@]31C)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C39H52O7/c1-34(44,22-40)20-26(41)18-27(33(43)45-5)28-12-16-39-21-38(28,39)15-13-30-35(2)14-11-25-17-29(24-9-7-6-8-10-24)46-23-36(25,3)31(35)19-32(42)37(30,39)4/h6-11,13,15,27-32,40,42,44H,12,14,16-23H2,1-5H3/t27?,28?,29-,30+,31+,32+,34?,35+,36-,37-,38+,39+/m0/s1

> <INCHI_KEY>
ALPNOVCGOWNGSI-LAGWCKPZSA-N

> <FORMULA>
C39H52O7

> <MOLECULAR_WEIGHT>
632.838

> <EXACT_MASS>
632.371304014

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
98

> <JCHEM_AVERAGE_POLARIZABILITY>
72.2542424804798

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 6,7-dihydroxy-2-[(1S,2R,3R,5R,6R,9S,14S,15R,18S)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0^{1,18}.0^{2,15}.0^{5,14}.0^{6,11}]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate

> <JCHEM_LOGP>
3.6861070263333326

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.25596943825541

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.885546498635566

> <JCHEM_PKA_STRONGEST_BASIC>
-0.1660955797634448

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
177.1031

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 6,7-dihydroxy-2-[(1S,2R,3R,5R,6R,9S,14S,15R,18S)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0^{1,18}.0^{2,15}.0^{5,14}.0^{6,11}]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate

> <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       0.965  -4.625   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.668  -3.114   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.790  -2.616   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.950  -3.629   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.087  -1.105   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.544  -0.606   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -3.704  -1.619   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -3.407  -3.130   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -5.161  -1.121   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.321  -2.134   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.308  -3.294   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -7.334  -0.974   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -7.481  -3.147   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -8.939  -2.649   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.073  -0.092   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.065   1.442   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.352   2.047   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.365   0.887   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.114  -0.458   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.574  -0.435   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.324  -1.780   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.864  -1.803   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.654  -0.482   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.194  -0.505   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.404  -1.827   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.943  -1.850   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.483  -1.874   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       9.273  -0.552   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.813  -0.575   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      11.604   0.747   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      13.143   0.723   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.934   2.045   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      15.473   2.022   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      16.223   0.676   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      15.433  -0.645   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.893  -0.622   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      10.854   2.092   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       9.314   2.115   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.524   0.793   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.774   2.139   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.984   0.817   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.234   2.162   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.695   2.185   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       3.945   3.531   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       3.904   0.864   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       3.155   2.209   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   15                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14                                                       
CONECT   14   13                                                            
CONECT   15    5   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   45                                             
CONECT   19   18   20                                                       
CONECT   20   19   15   18   21                                             
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   45                                                  
CONECT   24   23   25   26   41                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   39                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   37                                                  
CONECT   31   30   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   31                                                       
CONECT   37   30   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   28   40   41                                             
CONECT   40   39                                                            
CONECT   41   39   24   42                                                  
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   23   18   46                                             
CONECT   46   45                                                            
MASTER        0    0    0    0    0    0    0    0   46    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₉H₅₂O₇

Average Mass

632.8380 Da

Monoisotopic Mass

632.37130 Da

IUPAC Name

methyl 6,7-dihydroxy-2-[(1S,2R,3R,5R,6R,9S,14S,15R,18S)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0^{1,18}.0^{2,15}.0^{5,14}.0^{6,11}]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate

Traditional Name

methyl 6,7-dihydroxy-2-[(1S,2R,3R,5R,6R,9S,14S,15R,18S)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0^{1,18}.0^{2,15}.0^{5,14}.0^{6,11}]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate

CAS Registry Number

Not Available

SMILES

COC(=O)C(CC(=O)CC(C)(O)CO)C1CC[C@]23C[C@]12C=C[C@@H]1[C@@]2(C)CC=C4C[C@H](OC[C@]4(C)[C@@H]2C[C@@H](O)[C@@]31C)C1=CC=CC=C1

InChI Identifier

InChI=1S/C39H52O7/c1-34(44,22-40)20-26(41)18-27(33(43)45-5)28-12-16-39-21-38(28,39)15-13-30-35(2)14-11-25-17-29(24-9-7-6-8-10-24)46-23-36(25,3)31(35)19-32(42)37(30,39)4/h6-11,13,15,27-32,40,42,44H,12,14,16-23H2,1-5H3/t27?,28?,29-,30+,31+,32+,34?,35+,36-,37-,38+,39+/m0/s1

InChI Key

ALPNOVCGOWNGSI-LAGWCKPZSA-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
Dichapetalum madagascariense	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Bile acid, alcohol, or derivatives
Naphthopyran
Naphthalene
Fatty alcohol
Gamma-keto acid
Fatty acid ester
Fatty acyl
Benzenoid
Pyran
Oxane
Keto acid
Beta-hydroxy ketone
Monocyclic benzene moiety
Methyl ester
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
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
logP	3.69	ChemAxon
pKa (Strongest Acidic)	13.89	ChemAxon
pKa (Strongest Basic)	-0.17	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	177.1 m³·mol⁻¹	ChemAxon
Polarizability	72.25 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

102003025

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate (NP0254915)

MOL for NP0254915 (methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate)

3D MOL for NP0254915 (methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate)

3D SDF for NP0254915 (methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate)

3D-SDF for NP0254915 (methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate)

PDB for NP0254915 (methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate)

3D PDB for NP0254915 (methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate)

SMILES for NP0254915 (methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate)

INCHI for NP0254915 (methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate)

Structure for NP0254915 (methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate)

3D Structure for NP0254915 (methyl 6,7-dihydroxy-2-[(1s,2r,3r,5r,6r,9s,14s,15r,18s)-3-hydroxy-2,6,14-trimethyl-9-phenyl-8-oxahexacyclo[16.3.1.0¹,¹⁸.0²,¹⁵.0⁵,¹⁴.0⁶,¹¹]docosa-11,16-dien-19-yl]-6-methyl-4-oxoheptanoate)