NP-MRD: Showing NP-Card for 2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate (NP0319403)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 20:24:43 UTC

Updated at

2022-09-11 20:24:43 UTC

NP-MRD ID

NP0319403

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate

Description

2-(4A,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6H,6aH,7H,8H,10aH-benzo[c]isochromene-2-carboxylate belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton. 2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate is found in Cannabis sativa. 2-(4A,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6H,6aH,7H,8H,10aH-benzo[c]isochromene-2-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241501222D          

 41 45  0  0  0  0            999 V2000
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   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
    0.4323   -2.0127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -1.0942    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
   -0.0000    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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   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
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4138    0.5230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   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
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
  8 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 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  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 32 38  1  0  0  0  0
 38 39  1  0  0  0  0
 29 39  1  0  0  0  0
 37 40  1  0  0  0  0
 16 41  1  0  0  0  0
M  END

     RDKit          3D

 95 99  0  0  0  0  0  0  0  0999 V2000
   -3.3807    7.1006   -0.1186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7919    5.8032   -0.7651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7191    4.7285   -0.5583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5697    4.5436    0.9331 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5475    3.4859    1.3020 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9247    2.1365    0.8309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2132    1.8566    0.4288 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5786    0.6050   -0.0242 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6723   -0.4030   -0.0892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3788   -0.1748    0.3023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3897   -1.1422    0.2755 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0068    1.1179    0.7688 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3703    1.2773    1.1856 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7724    2.3824    1.6092 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2809    0.1999    1.1238 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5893    0.4470    1.5458 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1771    1.5397    0.6830 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5382    0.8890    2.9798 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3878   -0.8325    1.4593 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8147   -0.6037    1.9080 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5344   -1.9334    1.8160 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8516   -2.1364    0.3311 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9152   -3.6387    0.1197 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1934   -1.5481    0.0700 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2861   -0.7462   -1.1975 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3483   -1.2338   -2.2697 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9608   -1.0951   -1.7270 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8801   -0.5036   -2.5272 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7656   -1.5364   -0.4863 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4090   -1.4186    0.0871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0700   -1.7379   -0.5889 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2594   -2.6096    0.5716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1826   -3.5112    0.6644 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3141   -4.3796    1.9087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1489   -3.7498   -0.4126 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8055   -3.0976   -1.6952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2235   -1.7064   -1.5453 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2059   -0.6201   -1.3691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6036   -1.0975   -0.9535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4403    0.1691   -2.6724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8621    0.3487   -0.4173 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8958    7.9669   -0.5810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6256    7.1323    0.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2855    7.2971   -0.2425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7385    5.4803   -0.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9534    5.9492   -1.8328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8863    3.8354   -1.1391 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7490    5.2450   -0.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1734    5.5056    1.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5383    4.3818    1.4411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3593    3.5686    2.3813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6153    3.8169    0.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9508    2.6262    0.4891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5879   -2.0668   -0.0205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4118    1.9573   -0.0023 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5862    2.3361    1.3274 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0043    1.1822    0.0496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0249    1.8955    3.1070 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4803    1.0087    3.3567 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0256    0.1725    3.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9227   -1.5279    2.2185 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3109    0.0697    1.1506 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8840   -0.1700    2.9262 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4707   -1.8220    2.4094 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8603   -2.6992    2.2002 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8961   -4.0896    0.1734 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3886   -3.9131   -0.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4940   -4.0466    0.9787 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9818   -2.3516    0.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5235   -0.8835    0.9031 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0310    0.3167   -1.0005 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3246   -0.7405   -1.5965 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5401   -2.2662   -2.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5114   -0.5873   -3.1589 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2589   -0.3733   -3.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5511    0.4907   -2.2029 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9985   -1.1990   -2.6527 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7155   -0.8452   -0.5462 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0098   -2.4649    0.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1429   -2.1359   -1.1186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5301   -2.4450    1.4032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1127   -5.1124    1.8120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3231   -4.7956    2.1739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5514   -3.6459    2.7299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2051   -3.5977   -0.0902 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1192   -4.8757   -0.5774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9779   -3.7196   -2.1567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6107   -3.1115   -2.4347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7387   -1.5225   -2.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9957   -1.8928   -1.5777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6710   -1.2586    0.1392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2657   -0.1987   -1.1449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4636    0.5204   -2.7617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6783    0.9714   -2.7763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2477   -0.5428   -3.5044 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  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 31  1  0
 31 32  1  0
 32 33  2  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 38 40  1  0
 38 41  1  0
  9 10  1  0
 10 11  1  0
 10 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  1
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  2  0
 29 30  1  0
 12  6  1  0
 30 19  1  0
 41  8  1  0
 29 22  1  0
 37 31  1  0
  1 42  1  0
  1 43  1  0
  1 44  1  0
  2 45  1  0
  2 46  1  0
  3 47  1  0
  3 48  1  0
  4 49  1  0
  4 50  1  0
  5 51  1  0
  5 52  1  0
  7 53  1  0
 31 80  1  6
 32 81  1  0
 34 82  1  0
 34 83  1  0
 34 84  1  0
 35 85  1  0
 35 86  1  0
 36 87  1  0
 36 88  1  0
 37 89  1  6
 39 90  1  0
 39 91  1  0
 39 92  1  0
 40 93  1  0
 40 94  1  0
 40 95  1  0
 11 54  1  0
 17 55  1  0
 17 56  1  0
 17 57  1  0
 18 58  1  0
 18 59  1  0
 18 60  1  0
 19 61  1  1
 20 62  1  0
 20 63  1  0
 21 64  1  0
 21 65  1  0
 23 66  1  0
 23 67  1  0
 23 68  1  0
 24 69  1  0
 24 70  1  0
 25 71  1  0
 25 72  1  0
 26 73  1  0
 26 74  1  0
 28 75  1  0
 28 76  1  0
 28 77  1  0
 30 78  1  0
 30 79  1  0
M  END


  Mrv1533004241501222D          

 41 45  0  0  0  0            999 V2000
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   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
    0.4323   -2.0127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0980   -1.0942    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
   -0.0000    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
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 O   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
    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 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4138    0.5230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5888    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 C   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
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
  8 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
  6 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 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  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 32 38  1  0  0  0  0
 38 39  1  0  0  0  0
 29 39  1  0  0  0  0
 37 40  1  0  0  0  0
 16 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0319403

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC1=CC2=C(C3C=C(C)CCC3C(C)(C)O2)C(O)=C1C(=O)OC(C)(C)C1CCC2(C)CCCC(C)=C2C1

> <INCHI_IDENTIFIER>
InChI=1S/C37H54O4/c1-9-10-11-14-25-21-30-32(27-20-23(2)15-16-28(27)36(6,7)40-30)33(38)31(25)34(39)41-35(4,5)26-17-19-37(8)18-12-13-24(3)29(37)22-26/h20-21,26-28,38H,9-19,22H2,1-8H3

> <INCHI_KEY>
LTBABPUGMQQBAI-UHFFFAOYSA-N

> <FORMULA>
C37H54O4

> <MOLECULAR_WEIGHT>
562.835

> <EXACT_MASS>
562.402210219

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
95

> <JCHEM_AVERAGE_POLARIZABILITY>
68.593377160346

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6H,6aH,7H,8H,10aH-benzo[c]isochromene-2-carboxylate

> <ALOGPS_LOGP>
8.37

> <JCHEM_LOGP>
10.546347563000001

> <ALOGPS_LOGS>
-6.49

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.51047841984251

> <JCHEM_PKA_STRONGEST_BASIC>
-4.115300381685201

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
169.66490000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.84e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6aH,7H,8H,10aH-benzo[c]isochromene-2-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.807  -3.757   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.183  -2.043   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.000   1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       8.002   1.540   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.106   0.976   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.566   3.644   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      10.669   3.080   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.003   5.390   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      13.337   4.620   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      13.337   6.160   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      14.670   5.390   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      16.004   4.620   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      16.004   3.080   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      14.670   2.310   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      13.337   3.080   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      12.003   2.310   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      14.670   0.770   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   19                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   41                                                  
CONECT   17   16   18                                                       
CONECT   18   17   13   19                                                  
CONECT   19   18    8   20                                                  
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    6   23                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26   30   39                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34   38                                             
CONECT   33   32                                                            
CONECT   34   32   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   40                                                  
CONECT   38   37   32   39                                                  
CONECT   39   38   29                                                       
CONECT   40   37                                                            
CONECT   41   16                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

View in JSmol

Synonyms

Value	Source
2-(4a,8-Dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6H,6ah,7H,8H,10ah-benzo[c]isochromene-2-carboxylic acid	Generator

Chemical Formula

C₃₇H₅₄O₄

Average Mass

562.8350 Da

Monoisotopic Mass

562.40221 Da

IUPAC Name

2-(4a,8-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6H,6aH,7H,8H,10aH-benzo[c]isochromene-2-carboxylate

Traditional Name

2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6aH,7H,8H,10aH-benzo[c]isochromene-2-carboxylate

CAS Registry Number

Not Available

SMILES

CCCCCC1=CC2=C(C3C=C(C)CCC3C(C)(C)O2)C(O)=C1C(=O)OC(C)(C)C1CCC2(C)CCCC(C)=C2C1

InChI Identifier

InChI=1S/C37H54O4/c1-9-10-11-14-25-21-30-32(27-20-23(2)15-16-28(27)36(6,7)40-30)33(38)31(25)34(39)41-35(4,5)26-17-19-37(8)18-12-13-24(3)29(37)22-26/h20-21,26-28,38H,9-19,22H2,1-8H3

InChI Key

LTBABPUGMQQBAI-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
Cannabis sativa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids. These are sesquiterpenoids with a structure based on the eudesmane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids

Alternative Parents

Substituents

Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoid
2,2-dimethyl-1-benzopyran
Chromane
Benzopyran
Salicylic acid or derivatives
1-benzopyran
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Benzenoid
Vinylogous acid
Carboxylic acid ester
Monocarboxylic acid or derivatives
Oxacycle
Ether
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
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	8.37	ALOGPS
logP	10.55	ChemAxon
logS	-6.5	ALOGPS
pKa (Strongest Acidic)	9.51	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	169.66 m³·mol⁻¹	ChemAxon
Polarizability	68.59 Å³	ChemAxon
Number of Rings	5	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

74336922

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate (NP0319403)

MOL for NP0319403 (2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate)

3D MOL for NP0319403 (2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate)

3D SDF for NP0319403 (2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate)

3D-SDF for NP0319403 (2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate)

PDB for NP0319403 (2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate)

3D PDB for NP0319403 (2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate)

SMILES for NP0319403 (2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate)

INCHI for NP0319403 (2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate)

Structure for NP0319403 (2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate)

3D Structure for NP0319403 (2-(4a,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalen-2-yl)propan-2-yl 1-hydroxy-6,6,9-trimethyl-3-pentyl-6ah,7h,8h,10ah-benzo[c]isochromene-2-carboxylate)