NP-MRD: Showing NP-Card for (4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid (NP0216191)

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Record Information

Version

2.0

Created at

2022-09-05 16:03:19 UTC

Updated at

2022-09-05 16:03:19 UTC

NP-MRD ID

NP0216191

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid

Description

(4AR,5S,6R,8aR)-5-{2-[(1R,2R,6S,9R,11S,13R,14S,17S,18S)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]Henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-1-carboxylic acid belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid is found in Salvia wagneriana. Based on a literature review very few articles have been published on (4aR,5S,6R,8aR)-5-{2-[(1R,2R,6S,9R,11S,13R,14S,17S,18S)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]Henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-1-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052218032D          

 47 55  0  0  1  0            999 V2000
    5.5560    3.0438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1089    2.4315    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9156    2.6041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4685    1.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2146    1.2068    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0213    1.3794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7675    0.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5742    0.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1271    0.1547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8281    1.5521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5136   -0.1905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7069   -0.3631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1540    0.2492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4079    1.0342    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8550    1.6465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2237    1.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0616    1.8729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4690    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6756    1.5253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3711    2.2958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5983    2.0578    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4093    1.1045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9503    0.9868    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8126    1.1184    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1617    0.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9800    0.2304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6606   -0.2922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9545    0.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8930    0.9576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3200    0.3019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5015    0.2407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9042    0.9545    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3907    0.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7121    1.1217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8027    1.9417    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5193    2.3504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2712    2.0109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8265    2.6210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4178    3.3377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6099    3.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0508    2.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4955    1.6711    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1561    2.4231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3500    1.6580    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5792    2.4566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3656    2.6531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8528    1.9913    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  7 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 23 22  1  1  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 28  1  1  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 36 40  2  0  0  0  0
 35 41  1  0  0  0  0
 41 42  1  0  0  0  0
 32 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 29 44  1  0  0  0  0
 44 45  1  1  0  0  0
 45 46  2  0  0  0  0
 47 46  1  6  0  0  0
 21 47  1  0  0  0  0
 24 47  1  0  0  0  0
M  END

     RDKit          3D

 97105  0  0  0  0  0  0  0  0999 V2000
   -3.2871    1.5340   -2.9779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7667    0.3523   -2.2228 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2412    0.2980   -2.2199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5543   -1.1669   -1.8432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2052   -1.2546   -0.4074 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3021   -0.4864    0.3417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3342   -2.6426    0.1010 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9672   -3.6657   -0.6715 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4471   -3.4664   -1.8038 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0964   -4.9930   -0.2035 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8318   -2.8894    1.2988 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1649   -1.8929    2.1434 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9450   -0.5538    1.4759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8353   -0.7981   -0.0052 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1611    0.2494   -0.8016 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4215    1.6126   -0.1950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7438   -0.0238   -1.1452 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6811   -0.2131   -0.1902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3377    0.8917    0.7382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3797    0.8354    2.0670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2727    2.2309    2.5345 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7355    2.9296    1.3859 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1223    2.2667    0.4480 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4072    2.6785    1.0127 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6215    4.1228    0.6721 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6703    4.9488    0.5794 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9609    4.3207    0.5011 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6373    3.1744    1.0535 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6760    2.0721    0.5767 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.7982    2.0899   -0.9302 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1779    1.5892   -1.3820 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3490    0.2343   -0.8257 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3768   -0.6975   -1.4647 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6105   -0.3349   -0.9999 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6852   -1.4076   -0.1309 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7220   -2.7263   -0.7549 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5065   -3.0514   -1.8448 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2860   -4.3729   -2.1597 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4161   -4.8218   -1.3071 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0475   -3.8905   -0.4526 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5117   -1.2739    0.8550 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2932    0.2184    0.7019 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4916    0.8666    1.3225 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9806    0.7342    1.1674 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9183    0.8331    2.6427 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0882    1.7025    3.1947 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1792    2.6250    2.5029 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6767    1.2558   -3.8887 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.5778    0.3818   -3.2727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6669   -1.2290   -1.9235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0034   -1.8045   -2.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5105   -0.9279    1.3377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2672   -0.6540   -0.2265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1587    0.5880    0.3543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8897   -5.5675   -0.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9191   -3.8906    1.6777 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.0725   -0.0499    1.9161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1659   -1.7134   -0.0900 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.6731   -1.1836    0.3643 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2756   -0.3136   -0.8053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4718   -0.0245    2.7163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8078    2.4774    3.4266 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5974    3.1666    0.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6168    3.3120    2.1282 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0525    1.3948   -1.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0661    1.4750   -2.5001 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9750    2.3042   -1.2348 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9211   -0.2036   -2.3749 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8373   -1.6222   -1.8817 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2173    1.5301    2.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.1613    1.3712    0.5788 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5529    0.1933    3.2853 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3266    3.6349    2.9900 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  1
  5 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  7  2  0
  7  8  1  0
  8 10  1  0
  8  9  2  0
 14 15  1  0
 15 16  1  1
 15 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
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 24 47  1  0
 47 46  1  0
 46 45  2  0
 45 44  1  0
 44 42  1  0
 42 43  1  1
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 41 35  1  0
 35 34  1  0
 34 32  1  0
 32 33  1  6
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 31 30  1  0
 29 30  1  6
 29 28  1  0
 28 27  1  0
 27 25  1  0
 25 26  2  0
 35 36  1  0
 36 40  2  0
 40 39  1  0
 39 38  1  0
 38 37  2  0
 15  2  1  0
 23 19  1  0
 29 24  1  0
 37 36  1  0
  7  5  1  0
 47 21  1  0
 29 44  1  0
 24 25  1  6
 32 42  1  0
  1 48  1  0
  1 49  1  0
  1 50  1  0
  2 51  1  6
  3 52  1  0
  3 53  1  0
  4 54  1  0
  4 55  1  0
  6 56  1  0
  6 57  1  0
  6 58  1  0
 14 65  1  1
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 13 64  1  0
 12 61  1  0
 12 62  1  0
 11 60  1  0
 10 59  1  0
 16 66  1  0
 16 67  1  0
 16 68  1  0
 17 69  1  0
 17 70  1  0
 18 71  1  0
 18 72  1  0
 20 73  1  0
 21 74  1  1
 23 75  1  6
 47 97  1  1
 46 96  1  0
 45 95  1  0
 44 94  1  6
 43 91  1  0
 43 92  1  0
 43 93  1  0
 41 89  1  0
 41 90  1  0
 35 85  1  1
 33 82  1  0
 33 83  1  0
 33 84  1  0
 31 80  1  0
 31 81  1  0
 30 78  1  0
 30 79  1  0
 28 76  1  0
 28 77  1  0
 40 88  1  0
 38 87  1  0
 37 86  1  0
M  END


  Mrv1652309052218032D          

 47 55  0  0  1  0            999 V2000
    5.5560    3.0438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1089    2.4315    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9156    2.6041    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4685    1.9918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2146    1.2068    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0213    1.3794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7675    0.5945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5742    0.7671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1271    0.1547    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8281    1.5521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5136   -0.1905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7069   -0.3631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1540    0.2492    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4079    1.0342    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8550    1.6465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2237    1.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0616    1.8729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4690    1.2990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6756    1.5253    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3711    2.2958    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5983    2.0578    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4093    1.1045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9503    0.9868    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8126    1.1184    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1617    0.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9800    0.2304    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6606   -0.2922    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9545    0.0901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8930    0.9576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3200    0.3019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5015    0.2407    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9042    0.9545    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3907    0.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7121    1.1217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8027    1.9417    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5193    2.3504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2712    2.0109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8265    2.6210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4178    3.3377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6099    3.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0508    2.2813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4955    1.6711    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1561    2.4231    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3500    1.6580    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5792    2.4566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3656    2.6531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8528    1.9913    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  7 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  6  0  0  0
  5 14  1  0  0  0  0
 14 15  1  0  0  0  0
  2 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  6  0  0  0
 23 22  1  1  0  0  0
 19 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 28  1  1  0  0  0
 24 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 36 40  2  0  0  0  0
 35 41  1  0  0  0  0
 41 42  1  0  0  0  0
 32 42  1  0  0  0  0
 42 43  1  1  0  0  0
 42 44  1  0  0  0  0
 29 44  1  0  0  0  0
 44 45  1  1  0  0  0
 45 46  2  0  0  0  0
 47 46  1  6  0  0  0
 21 47  1  0  0  0  0
 24 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0216191

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@]2(C)[C@H](CCC=C2C(O)=O)[C@@]1(C)CCC1=C[C@@H]2O[C@H]1[C@@]13[C@@H]2C=C[C@@H]2[C@@]4(C)C[C@H](O[C@]4(C)CC[C@@]12COC3=O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C40H50O7/c1-23-11-14-36(3)27(33(41)42)7-6-8-30(36)35(23,2)15-12-24-19-28-26-9-10-31-37(4)20-29(25-13-18-44-21-25)47-38(37,5)16-17-39(31)22-45-34(43)40(26,39)32(24)46-28/h7,9-10,13,18-19,21,23,26,28-32H,6,8,11-12,14-17,20,22H2,1-5H3,(H,41,42)/t23-,26-,28+,29+,30-,31-,32-,35+,36+,37-,38-,39+,40-/m1/s1

> <INCHI_KEY>
HLWXOXRRWFGBKK-SKWFETBXSA-N

> <FORMULA>
C40H50O7

> <MOLECULAR_WEIGHT>
642.833

> <EXACT_MASS>
642.35565395

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
70.4952222457946

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4aR,5S,6R,8aR)-5-{2-[(1R,2R,6S,9R,11S,13R,14S,17S,18S)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0^{2,6}.0^{2,17}.0^{6,14}.0^{9,13}]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-1-carboxylic acid

> <JCHEM_LOGP>
6.476570123666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.706199852417265

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8504518637589724

> <JCHEM_POLAR_SURFACE_AREA>
95.2

> <JCHEM_REFRACTIVITY>
177.81219999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(4aR,5S,6R,8aR)-5-{2-[(1R,2R,6S,9R,11S,13R,14S,17S,18S)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0^{2,6}.0^{2,17}.0^{6,14}.0^{9,13}]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid

> <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      10.371   5.682   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.403   4.539   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.909   4.861   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.941   3.718   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.467   2.253   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.973   2.575   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      14.499   1.110   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.005   1.432   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      17.037   0.289   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      16.479   2.897   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      14.025  -0.356   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.519  -0.678   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.487   0.465   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.961   1.930   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.929   3.074   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.751   2.082   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.448   3.496   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.342   2.425   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.861   2.847   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.293   4.285   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.850   3.841   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       4.497   2.062   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       5.507   1.842   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.384   2.088   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.035   0.626   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.563   0.430   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       3.100  -0.545   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       1.782   0.168   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.667   1.788   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.597   0.564   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.936   0.449   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.688   1.782   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.596   0.538   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -3.196   2.094   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -3.365   3.625   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -4.703   4.387   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -6.106   3.754   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -7.143   4.893   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -6.380   6.230   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      -4.872   5.918   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -1.961   4.258   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.925   3.119   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      -0.291   4.523   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       0.653   3.095   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       1.081   4.586   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.549   4.952   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       3.459   3.717   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   15                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   14                                             
CONECT    6    5                                                            
CONECT    7    5    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    5   15                                                  
CONECT   15   14    2   16   17                                             
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   47                                                  
CONECT   22   21   23                                                       
CONECT   23   22   19   24                                                  
CONECT   24   23   25   29   47                                             
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   24   30   44                                             
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34   42                                             
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36   41                                                  
CONECT   36   35   37   40                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   36                                                       
CONECT   41   35   42                                                       
CONECT   42   41   32   43   44                                             
CONECT   43   42                                                            
CONECT   44   42   29   45                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   21   24                                                  
MASTER        0    0    0    0    0    0    0    0   47    0  110    0
END

View in JSmol

Synonyms

Value	Source
(4AR,5S,6R,8ar)-5-{2-[(1R,2R,6S,9R,11S,13R,14S,17S,18S)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0,.0,.0,.0,]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-1-carboxylate	Generator

Chemical Formula

C₄₀H₅₀O₇

Average Mass

642.8330 Da

Monoisotopic Mass

642.35565 Da

IUPAC Name

(4aR,5S,6R,8aR)-5-{2-[(1R,2R,6S,9R,11S,13R,14S,17S,18S)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0^{2,6}.0^{2,17}.0^{6,14}.0^{9,13}]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,5,6,7,8,8a-octahydronaphthalene-1-carboxylic acid

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@]2(C)[C@H](CCC=C2C(O)=O)[C@@]1(C)CCC1=C[C@@H]2O[C@H]1[C@@]13[C@@H]2C=C[C@@H]2[C@@]4(C)C[C@H](O[C@]4(C)CC[C@@]12COC3=O)C1=COC=C1

InChI Identifier

InChI=1S/C40H50O7/c1-23-11-14-36(3)27(33(41)42)7-6-8-30(36)35(23,2)15-12-24-19-28-26-9-10-31-37(4)20-29(25-13-18-44-21-25)47-38(37,5)16-17-39(31)22-45-34(43)40(26,39)32(24)46-28/h7,9-10,13,18-19,21,23,26,28-32H,6,8,11-12,14-17,20,22H2,1-5H3,(H,41,42)/t23-,26-,28+,29+,30-,31-,32-,35+,36+,37-,38-,39+,40-/m1/s1

InChI Key

HLWXOXRRWFGBKK-SKWFETBXSA-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
Salvia wagneriana	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
19-oxosteroid
Clerodane diterpenoid
Oxosteroid
Steroid
Naphthofuran
Dicarboxylic acid or derivatives
Gamma butyrolactone
Tetrahydrofuran
Heteroaromatic compound
Dihydrofuran
Furan
Carboxylic acid ester
Lactone
Organoheterocyclic compound
Oxacycle
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Ether
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
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
logP	6.48	ChemAxon
pKa (Strongest Acidic)	4.71	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	95.2 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	177.81 m³·mol⁻¹	ChemAxon
Polarizability	70.5 Å³	ChemAxon
Number of Rings	9	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

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

162966717

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid (NP0216191)

MOL for NP0216191 ((4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid)

3D MOL for NP0216191 ((4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid)

3D SDF for NP0216191 ((4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid)

3D-SDF for NP0216191 ((4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid)

PDB for NP0216191 ((4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid)

3D PDB for NP0216191 ((4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid)

SMILES for NP0216191 ((4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid)

INCHI for NP0216191 ((4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid)

Structure for NP0216191 ((4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid)

3D Structure for NP0216191 ((4ar,5s,6r,8ar)-5-{2-[(1r,2r,6s,9r,11s,13r,14s,17s,18s)-11-(furan-3-yl)-9,13-dimethyl-3-oxo-4,10,21-trioxahexacyclo[16.2.1.0²,⁶.0²,¹⁷.0⁶,¹⁴.0⁹,¹³]henicosa-15,19-dien-20-yl]ethyl}-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid)