NP-MRD: Showing NP-Card for 1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate (NP0164769)

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Record Information

Version

2.0

Created at

2022-09-02 23:42:57 UTC

Updated at

2022-09-02 23:42:58 UTC

NP-MRD ID

NP0164769

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate

Description

1-[5-(1,2,4A,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations. 1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate is found in Parentucellia latifolia. Based on a literature review very few articles have been published on 1-[5-(1,2,4a,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032201422D          

 47 50  0  0  0  0            999 V2000
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6157   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4282   -2.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8979   -1.4803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2406   -1.9690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7709   -2.6010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4888   -3.3762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3012   -3.2330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0191   -4.0082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8315   -3.8650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7369   -4.7835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9244   -4.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3941   -4.2947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6763   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  4  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 24 31  1  0  0  0  0
 18 31  1  0  0  0  0
  2 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  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  1  0  0  0  0
 40 42  1  0  0  0  0
 40 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 34 46  1  0  0  0  0
 39 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END

     RDKit          3D

115118  0  0  0  0  0  0  0  0999 V2000
   -6.9557    4.3579   -0.2393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6473    3.0142   -0.1790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5798    2.8774    0.7019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3461    1.6428    0.8849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9201    0.4824    0.0590 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.0510   -0.5256   -0.1321 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4286   -0.9184    1.3169 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2770   -0.0280   -0.7703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4666   -1.7463   -0.7550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9658   -1.7456   -0.8499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3770   -0.5318   -1.4981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1309    0.7540   -1.1705 C   0  0  1  0  0  0  0  0  0  0  0  0
   -9.0761    0.9287   -2.3839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2583    1.9196   -1.1015 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.8351    1.9015   -1.4604 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7829    1.8571   -0.4446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6554    0.7721    0.4950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6315    0.4485    1.5500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5415    0.0024    0.4770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3135   -1.0934    1.4474 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1415   -0.8309    2.1753 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8735   -0.6789    1.6892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7109   -0.7789    0.4502 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3066   -0.4058    2.5412 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5083   -0.3035    1.7053 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8546    0.7971    1.2101 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3244   -1.4039    1.4167 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5008   -1.1805    0.5857 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1116   -2.5280    0.4774 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2925   -2.8845    0.8543 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6741   -4.3400    0.6488 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3034   -2.0385    1.4709 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6198   -1.9510    0.8400 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9160   -1.4552   -0.4978 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3172   -2.3342   -1.6067 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4575   -1.6802   -0.6687 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.8700   -1.7406   -2.0996 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2613   -0.8332    0.2286 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7233    0.5215    0.5013 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6943    0.9776   -0.5028 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.5181    1.4360   -1.7360 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1053    2.2243    0.0075 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8688    3.0469    0.9827 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9282    2.6438   -0.3665 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    1.7881   -1.3494 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2487    0.3917   -0.6601 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6864   -0.0392   -0.8689 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.3726    4.4450   -1.1664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3799    4.5669    0.6679 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8047    5.0897   -0.3580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8460    3.7132    1.3747 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4625    1.8315    0.8159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2470    1.4112    2.0045 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2193   -0.1193    0.7284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4998   -1.2412    1.8228 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8376   -0.0190    1.8304 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2065   -1.7087    1.2833 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1422   -0.6278   -0.3262 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5692    1.0055   -0.6130 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3891   -0.2730   -1.8695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7149   -2.6659   -0.1333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9145   -2.0158   -1.7532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6955   -2.6492   -1.4619 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5268   -1.9386    0.1601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3139   -0.5077   -1.2645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4162   -0.7427   -2.6133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4410    1.4748   -3.1485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9107    1.5798   -2.1902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2680   -0.0429   -2.8578 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6763    2.5194   -2.1329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5860    2.8365   -2.1167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5988    1.0875   -2.2213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7947    2.8510    0.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7967    2.0111   -1.0234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0301   -0.5884    1.4526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1136    0.5146    2.5673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4698    1.1412    1.6314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8156    0.2263   -0.2895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1404   -1.2087    2.1660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1894   -2.0645    0.8794 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2019    0.5863    3.0619 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3814   -1.1801    3.3334 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1283   -0.8135   -0.3720 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1228   -0.4322    1.0893 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4194   -3.2750    0.0072 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6650   -4.5758    1.0273 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5178   -4.5271   -0.4307 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8818   -4.9441    1.1706 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8601   -1.0893    1.8627 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5175   -2.5770    2.4847 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0883   -2.9918    0.9382 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2716   -1.3786    1.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8792   -3.2570   -1.7575 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2254   -2.4796   -1.4655 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3951   -1.7345   -2.5411 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5497   -2.7577   -0.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9043   -1.2743   -2.1591 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0113   -2.7909   -2.4663 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2756   -1.1843   -2.8166 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4021   -1.3431    1.2281 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3083   -0.8044   -0.1955 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5922    1.2435    0.3957 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4112    0.6691    1.5495 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5550    1.0392   -1.6876 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6311    2.5362   -1.7200 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0295    1.1780   -2.6753 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8885    3.1927    0.5549 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9078    2.5944    1.9944 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4017    4.0500    1.1232 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4517    3.5443   -0.0298 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7351    1.6612   -2.2960 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1583    2.0940   -1.5180 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5430   -0.2260   -1.1969 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0359    0.6261    0.3912 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7287   -0.0597   -2.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
 37 36  1  0
 36 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  6
 40 47  1  0
 47 46  1  0
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 47 34  1  0
 34 35  1  6
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 29 28  1  0
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 15 14  1  0
 14  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  1  0
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 12 13  1  6
 34 36  1  0
 12 14  1  0
 42 40  1  0
 12  5  1  0
 37 97  1  0
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 38100  1  0
 38101  1  0
 39102  1  0
 39103  1  0
 41104  1  0
 41105  1  0
 41106  1  0
 47115  1  6
 46113  1  0
 46114  1  0
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 45112  1  0
 44110  1  0
 43107  1  0
 43108  1  0
 43109  1  0
 35 93  1  0
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 32 89  1  0
 32 90  1  0
 31 86  1  0
 31 87  1  0
 31 88  1  0
 29 85  1  0
 28 83  1  0
 28 84  1  0
 24 81  1  0
 24 82  1  0
 20 79  1  0
 20 80  1  0
 19 78  1  0
 18 75  1  0
 18 76  1  0
 18 77  1  0
 16 73  1  0
 16 74  1  0
 15 71  1  0
 15 72  1  0
 14 70  1  6
  1 48  1  0
  1 49  1  0
  1 50  1  0
  3 51  1  0
  4 52  1  0
  4 53  1  0
  5 54  1  1
  7 55  1  0
  7 56  1  0
  7 57  1  0
  8 58  1  0
  8 59  1  0
  8 60  1  0
  9 61  1  0
  9 62  1  0
 10 63  1  0
 10 64  1  0
 11 65  1  0
 11 66  1  0
 13 67  1  0
 13 68  1  0
 13 69  1  0
M  END


  Mrv1652309032201422D          

 47 50  0  0  0  0            999 V2000
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6157   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4282   -2.1123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8979   -1.4803    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2406   -1.9690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7709   -2.6010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4888   -3.3762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3012   -3.2330    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0191   -4.0082    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8315   -3.8650    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7369   -4.7835    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9244   -4.9267    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3941   -4.2947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6763   -3.5195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  4  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 24 31  1  0  0  0  0
 18 31  1  0  0  0  0
  2 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 35 37  2  0  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  1  0  0  0  0
 40 42  1  0  0  0  0
 40 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 34 46  1  0  0  0  0
 39 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0164769

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCC2(C)C(CCC=C2C)C1(C)CCC(C)=CCOC(=O)CC(=O)OCC=C(C)CCC1C(C)=CCC2C(C)(C)CCCC12C

> <INCHI_IDENTIFIER>
InChI=1S/C43H68O4/c1-30(15-17-35-32(3)16-18-36-40(6,7)23-12-24-43(35,36)10)21-27-46-38(44)29-39(45)47-28-22-31(2)19-25-41(8)34(5)20-26-42(9)33(4)13-11-14-37(41)42/h13,16,21-22,34-37H,11-12,14-15,17-20,23-29H2,1-10H3

> <INCHI_KEY>
OZJBEUHJCWOKKL-UHFFFAOYSA-N

> <FORMULA>
C43H68O4

> <MOLECULAR_WEIGHT>
649.013

> <EXACT_MASS>
648.51176067

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
115

> <JCHEM_AVERAGE_POLARIZABILITY>
79.70554135414562

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-[5-(1,2,4a,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate

> <ALOGPS_LOGP>
9.71

> <JCHEM_LOGP>
11.200578533000002

> <ALOGPS_LOGS>
-7.04

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.194126933535006

> <JCHEM_PKA_STRONGEST_BASIC>
-6.857434128941894

> <JCHEM_POLAR_SURFACE_AREA>
52.60000000000001

> <JCHEM_REFRACTIVITY>
198.25600000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.93e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      12.003  -0.770   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      13.337   0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      13.337   1.540   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      14.670  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.004   0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      16.004   1.540   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      17.338  -0.770   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      18.672   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      20.005  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.005  -2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      18.672  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.339  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      21.339  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      22.673  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      21.683  -6.570   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      23.199  -3.943   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      22.209  -2.763   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      24.716  -3.675   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      25.706  -4.855   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.179  -6.302   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.696  -6.035   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      26.169  -7.482   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      27.686  -7.215   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      25.642  -8.929   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      24.126  -9.197   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      23.136  -8.017   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      23.662  -6.570   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      -0.527  -1.447   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -1.517   0.267   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       4.001   0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   32                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   31                                             
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   31                                             
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   24   18                                                  
CONECT   32    2   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   46                                                  
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   46                                                  
CONECT   40   39   41   42   43                                             
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   40   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   34   39   47                                             
CONECT   47   46                                                            
MASTER        0    0    0    0    0    0    0    0   47    0  100    0
END

View in JSmol

Synonyms

Value	Source
1-[5-(1,2,4a,5-Tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioic acid	Generator

Chemical Formula

C₄₃H₆₈O₄

Average Mass

649.0130 Da

Monoisotopic Mass

648.51176 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1CCC2(C)C(CCC=C2C)C1(C)CCC(C)=CCOC(=O)CC(=O)OCC=C(C)CCC1C(C)=CCC2C(C)(C)CCCC12C

InChI Identifier

InChI=1S/C43H68O4/c1-30(15-17-35-32(3)16-18-36-40(6,7)23-12-24-43(35,36)10)21-27-46-38(44)29-39(45)47-28-22-31(2)19-25-41(8)34(5)20-26-42(9)33(4)13-11-14-37(41)42/h13,16,21-22,34-37H,11-12,14-15,17-20,23-29H2,1-10H3

InChI Key

OZJBEUHJCWOKKL-UHFFFAOYSA-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
Parentucellia latifolia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Colensane and clerodane diterpenoids

Alternative Parents

Substituents

Clerodane 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	9.71	ALOGPS
logP	11.2	ChemAxon
logS	-7	ALOGPS
pKa (Strongest Acidic)	13.19	ChemAxon
pKa (Strongest Basic)	-6.9	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	198.26 m³·mol⁻¹	ChemAxon
Polarizability	79.71 Å³	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

163042377

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate (NP0164769)

MOL for NP0164769 (1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate)

3D MOL for NP0164769 (1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate)

3D SDF for NP0164769 (1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate)

3D-SDF for NP0164769 (1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate)

PDB for NP0164769 (1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate)

3D PDB for NP0164769 (1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate)

SMILES for NP0164769 (1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate)

INCHI for NP0164769 (1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate)

Structure for NP0164769 (1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate)

3D Structure for NP0164769 (1-[5-(1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] 3-[5-(2,5,5,8a-tetramethyl-1,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-yl] propanedioate)