NP-MRD: Showing NP-Card for 1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate (NP0157293)

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Record Information

Version

2.0

Created at

2022-09-02 14:38:37 UTC

Updated at

2022-09-02 14:38:37 UTC

NP-MRD ID

NP0157293

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate

Description

Bis(beyerane-15-ene-19-ol)malonate belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate is found in Helichrysum tenax. Based on a literature review very few articles have been published on Bis(beyerane-15-ene-19-ol)malonate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022216382D          

 47 54  0  0  1  0            999 V2000
   -5.6135   -2.4922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3087   -2.9364    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6254   -2.1746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1240   -1.5195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3059   -1.6261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9892   -2.3879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8045   -0.9709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9865   -1.0775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6698   -1.8393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4851   -0.4224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6670   -0.5290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1656    0.1262    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6075   -0.4813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8979    0.5062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9350    1.3303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2397    1.7745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5075    1.3945    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5515    2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4704    0.5704    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7367    0.1731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0341    0.6081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0181    1.4518    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8741    1.3709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2502    2.1549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6259    2.7510    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1179    3.4133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1266    3.1773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8659    2.7374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8055    1.8599    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2450    2.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7505   -3.5439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9976   -4.3311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8028   -4.5107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3610   -3.9032    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6014   -4.6924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1139   -3.1160    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6675   -2.4918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4765   -2.6602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7801   -3.4475    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.5908   -3.0664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2124   -3.6745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8296   -4.4481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.5184   -4.9022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2683   -5.1061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4232   -4.9456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1797   -4.1003    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.2543   -3.9812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  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
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 28  1  1  0  0  0
 22 29  1  0  0  0  0
 17 29  1  0  0  0  0
 25 30  1  0  0  0  0
 22 30  1  6  0  0  0
  2 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
  2 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  6  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 46 45  1  1  0  0  0
 39 46  1  0  0  0  0
 34 46  1  0  0  0  0
 42 47  1  0  0  0  0
 39 47  1  6  0  0  0
M  END

     RDKit          3D

111118  0  0  0  0  0  0  0  0999 V2000
    3.4966   -2.3072    1.4711 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0492   -2.0966    0.0404 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8619   -2.3375   -0.8554 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7888   -1.4617   -0.6463 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6446   -1.6177   -1.3912 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5124   -2.5184   -2.2596 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5212   -0.7107   -1.2025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3325   -1.2371   -0.0521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9363   -0.9042    1.0848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4160   -2.0147   -0.1695 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2921   -2.5921    0.7133 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1919   -1.7711    1.5430 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.9959   -2.8547    2.3685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5896   -0.9242    2.6223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5394    0.5303    2.3602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9050    1.0050    1.0002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9569    0.2978    0.2558 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5316    0.1915   -1.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2768   -1.0179    0.8654 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.0874   -1.8716   -0.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2554   -1.1691   -0.6600 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3377    0.2809   -0.5406 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.4596    0.9342   -1.8978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2771    1.9619   -1.8621 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6978    2.1772   -0.4492 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.0794    2.7364   -0.3232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6334    3.0174    0.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2811    2.4202   -0.2488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2930    1.0217    0.2227 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.6800    0.7330    0.0656 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9874   -3.2710   -0.1564 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1812   -3.1997    0.7570 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6277   -1.7894    1.0247 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2220   -0.8481   -0.0912 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.7902   -1.3314   -1.3760 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6943   -0.7769   -0.0727 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2521    0.1218   -1.1742 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7890    1.5180   -0.9353 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2403    1.5900   -0.6496 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.0849    1.7441   -1.8636 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1714    2.4743   -1.5566 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0575    2.9663   -0.1757 C   0  0  2  0  0  0  0  0  0  0  0  0
    8.6356    4.3158    0.0674 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6857    1.9665    0.7498 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1764    0.5658    0.5464 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7004    0.5318    0.2941 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5405    2.9271    0.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1153   -1.3461    1.8595 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6937   -3.0672    1.3828 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3018   -2.6723    2.1464 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1499   -2.4204   -1.9246 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4655   -3.3637   -0.5966 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1358    0.2825   -0.9098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1260   -0.5776   -2.0990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6202   -3.2522    1.3879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8598   -3.4214    0.1764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8975   -2.3765    2.7404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3174   -3.2114    3.1817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1305   -3.7025    1.6802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6343   -1.3223    2.9996 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2500   -1.0060    3.5802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4582    0.8493    2.5266 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0736    1.1350    3.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1082    2.1093    1.1239 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9577    1.0291    0.3768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0242   -0.6073   -1.7544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4296    0.2419   -1.3320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8787    1.1503   -1.6978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0116   -0.7869    1.7113 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4791   -2.7265    0.5574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4378   -2.3660   -0.8233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2706   -1.4497   -1.7576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2166   -1.6137   -0.2781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9285    0.5803   -2.7852 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5789    2.5409   -2.7380 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2151    3.6126   -0.9730 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8062    1.9281   -0.5429 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2298    2.9858    0.7554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7094    4.0258   -0.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7118    2.9719    1.3139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5392    3.1029    0.1399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3294    2.5299   -1.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6281    1.0368    1.3042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5254    0.2006   -0.3678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6135    0.7106    1.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2352   -3.4694   -1.2160 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3991   -4.1788    0.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0109   -3.6950    1.7335 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9870   -3.8152    0.2622 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3276   -1.4549    2.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7601   -1.8579    1.0766 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6131   -0.6614   -1.7668 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1029   -1.4712   -2.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3310   -2.3131   -1.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4782   -0.2008    0.8803 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5245   -0.2037   -2.1970 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1531    0.2274   -1.1672 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2386    1.9958   -0.0964 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5474    2.1203   -1.8358 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8805    1.3438   -2.8479 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9793    2.6469   -2.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5399    4.3296    0.6930 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8503    4.9238    0.6018 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7716    4.8327   -0.9072 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5333    2.3211    1.7983 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7817    1.9465    0.5797 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7797    0.0416   -0.1972 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3582    0.0348    1.5237 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2015    0.7509    1.2847 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1078    3.7764   -0.4819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2908    2.8904    1.1109 H   0  0  0  0  0  0  0  0  0  0  0  0
 42 43  1  6
 42 47  1  0
 47 39  1  0
 39 38  1  0
 38 37  1  0
 37 36  1  0
 36  2  1  0
  2  1  1  1
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  1 48  1  0
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 29 83  1  1
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 27 79  1  0
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 26 78  1  0
 30 84  1  0
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 21 72  1  0
 21 73  1  0
 20 70  1  0
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 19 69  1  1
 23 74  1  0
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 31 86  1  0
 31 87  1  0
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 32 89  1  0
 33 90  1  0
 33 91  1  0
 35 92  1  0
 35 93  1  0
 35 94  1  0
 46109  1  1
 45107  1  0
 45108  1  0
 44105  1  0
 44106  1  0
 40100  1  0
 41101  1  0
M  END


  Mrv1652309022216382D          

 47 54  0  0  1  0            999 V2000
   -5.6135   -2.4922    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3087   -2.9364    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.6254   -2.1746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1240   -1.5195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3059   -1.6261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9892   -2.3879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8045   -0.9709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9865   -1.0775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6698   -1.8393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4851   -0.4224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6670   -0.5290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1656    0.1262    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6075   -0.4813    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8979    0.5062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9350    1.3303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2397    1.7745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5075    1.3945    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5515    2.2184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4704    0.5704    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7367    0.1731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0341    0.6081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0181    1.4518    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8741    1.3709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2502    2.1549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6259    2.7510    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1179    3.4133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1266    3.1773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8659    2.7374    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8055    1.8599    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2450    2.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7505   -3.5439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9976   -4.3311    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8028   -4.5107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3610   -3.9032    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6014   -4.6924    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1139   -3.1160    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.6675   -2.4918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4765   -2.6602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7801   -3.4475    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.5908   -3.0664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2124   -3.6745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8296   -4.4481    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  -10.5184   -4.9022    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2683   -5.1061    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4232   -4.9456    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1797   -4.1003    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -9.2543   -3.9812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  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
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 29 28  1  1  0  0  0
 22 29  1  0  0  0  0
 17 29  1  0  0  0  0
 25 30  1  0  0  0  0
 22 30  1  6  0  0  0
  2 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
  2 36  1  0  0  0  0
 36 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  6  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 46 45  1  1  0  0  0
 39 46  1  0  0  0  0
 34 46  1  0  0  0  0
 42 47  1  0  0  0  0
 39 47  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0157293

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]12C[C@@]3(CC[C@H]4[C@@](C)(COC(=O)CC(=O)OC[C@@]5(C)CCC[C@]6(C)[C@H]7CC[C@]8(C)C[C@@]7(CC[C@@H]56)C=C8)CCC[C@]4(C)[C@H]3CC1)C=C2

> <INCHI_IDENTIFIER>
InChI=1S/C43H64O4/c1-36-17-9-32-40(5)15-7-13-38(3,30(40)11-19-42(32,26-36)23-21-36)28-46-34(44)25-35(45)47-29-39(4)14-8-16-41(6)31(39)12-20-43-24-22-37(2,27-43)18-10-33(41)43/h21-24,30-33H,7-20,25-29H2,1-6H3/t30-,31-,32+,33+,36-,37-,38+,39+,40-,41-,42+,43+/m0/s1

> <INCHI_KEY>
YSKDTUNRKSSWKE-JJNJUOAYSA-N

> <FORMULA>
C43H64O4

> <MOLECULAR_WEIGHT>
644.981

> <EXACT_MASS>
644.480460541

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
111

> <JCHEM_AVERAGE_POLARIZABILITY>
77.77943319269423

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,3-bis{[(1S,4R,5S,9R,10R,13R)-5,9,13-trimethyltetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadec-14-en-5-yl]methyl} propanedioate

> <ALOGPS_LOGP>
6.85

> <JCHEM_LOGP>
9.666063354333335

> <ALOGPS_LOGS>
-7.95

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.359412083928667

> <JCHEM_PKA_STRONGEST_BASIC>
-6.847985309558388

> <JCHEM_POLAR_SURFACE_AREA>
52.60000000000001

> <JCHEM_REFRACTIVITY>
189.3768

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.31e-06 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,3-bis{[(1S,4R,5S,9R,10R,13R)-5,9,13-trimethyltetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadec-14-en-5-yl]methyl} propanedioate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0     -10.478  -4.652   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -11.776  -5.481   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -12.367  -4.059   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0     -11.431  -2.836   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -9.904  -3.035   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -9.313  -4.457   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -8.968  -1.812   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -7.441  -2.011   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -6.850  -3.433   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -6.506  -0.788   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -4.978  -0.987   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.043   0.236   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.001  -0.899   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.409   0.945   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.479   2.483   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.181   3.312   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.814   2.603   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.896   4.141   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.745   1.065   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.375   0.323   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.064   1.135   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.034   2.710   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.632   2.559   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.334   4.022   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.168   5.135   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.087   6.371   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.236   5.931   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.616   5.110   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.504   3.472   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.457   3.949   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -10.734  -6.615   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -11.196  -8.085   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -12.699  -8.420   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -13.740  -7.286   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -14.189  -8.759   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -13.279  -5.817   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -14.313  -4.651   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -15.823  -4.966   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -16.389  -6.435   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -17.903  -5.724   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -19.063  -6.859   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0     -18.349  -8.303   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0     -19.634  -9.151   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -17.301  -9.531   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0     -15.723  -9.232   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -15.269  -7.654   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0     -17.275  -7.432   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   31   36                                             
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   19                                             
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   29                                             
CONECT   18   17                                                            
CONECT   19   17   12   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   29   30                                             
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27   30                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   22   17                                                  
CONECT   30   25   22                                                       
CONECT   31    2   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36   46                                             
CONECT   35   34                                                            
CONECT   36   34    2   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   46   47                                             
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43   44   47                                             
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   39   34                                                  
CONECT   47   42   39                                                       
MASTER        0    0    0    0    0    0    0    0   47    0  108    0
END

View in JSmol

Synonyms

Value	Source
Bis(beyerane-15-ene-19-ol)malonic acid	Generator

Chemical Formula

C₄₃H₆₄O₄

Average Mass

644.9810 Da

Monoisotopic Mass

644.48046 Da

IUPAC Name

1,3-bis{[(1S,4R,5S,9R,10R,13R)-5,9,13-trimethyltetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadec-14-en-5-yl]methyl} propanedioate

Traditional Name

1,3-bis{[(1S,4R,5S,9R,10R,13R)-5,9,13-trimethyltetracyclo[11.2.1.0^{1,10}.0^{4,9}]hexadec-14-en-5-yl]methyl} propanedioate

CAS Registry Number

Not Available

SMILES

C[C@]12C[C@@]3(CC[C@H]4[C@@](C)(COC(=O)CC(=O)OC[C@@]5(C)CCC[C@]6(C)[C@H]7CC[C@]8(C)C[C@@]7(CC[C@@H]56)C=C8)CCC[C@]4(C)[C@H]3CC1)C=C2

InChI Identifier

InChI=1S/C43H64O4/c1-36-17-9-32-40(5)15-7-13-38(3,30(40)11-19-42(32,26-36)23-21-36)28-46-34(44)25-35(45)47-29-39(4)14-8-16-41(6)31(39)12-20-43-24-22-37(2,27-43)18-10-33(41)43/h21-24,30-33H,7-20,25-29H2,1-6H3/t30-,31-,32+,33+,36-,37-,38+,39+,40-,41-,42+,43+/m0/s1

InChI Key

YSKDTUNRKSSWKE-JJNJUOAYSA-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
Helichrysum tenax	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Beyerane diterpenoid
1,3-dicarbonyl compound
Dicarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	6.85	ALOGPS
logP	9.67	ChemAxon
logS	-8	ALOGPS
pKa (Strongest Acidic)	12.36	ChemAxon
pKa (Strongest Basic)	-6.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	189.38 m³·mol⁻¹	ChemAxon
Polarizability	77.78 Å³	ChemAxon
Number of Rings	8	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

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

102175034

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate (NP0157293)

MOL for NP0157293 (1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate)

3D MOL for NP0157293 (1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate)

3D SDF for NP0157293 (1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate)

3D-SDF for NP0157293 (1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate)

PDB for NP0157293 (1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate)

3D PDB for NP0157293 (1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate)

SMILES for NP0157293 (1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate)

INCHI for NP0157293 (1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate)

Structure for NP0157293 (1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate)

3D Structure for NP0157293 (1,3-bis{[(1s,4r,5s,9r,10r,13r)-5,9,13-trimethyltetracyclo[11.2.1.0¹,¹⁰.0⁴,⁹]hexadec-14-en-5-yl]methyl} propanedioate)