NP-MRD: Showing NP-Card for 5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one (NP0326711)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 08:33:17 UTC

Updated at

2022-09-12 08:33:17 UTC

NP-MRD ID

NP0326711

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one

Description

5-(2-{5-Methoxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-9-en-14-yl}propyl)-3-methyl-2,5-dihydrofuran-2-one belongs to the class of organic compounds known as withanolides and derivatives. These are c28 steroids structurally characterized by an ergostane skeleton usually functionalized at carbons 1, 22 and 26 to form a lactone ring. 5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one is found in Abies mariesii, Abies sibirica and Abies veitchii. 5-(2-{5-Methoxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-9-en-14-yl}propyl)-3-methyl-2,5-dihydrofuran-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201501372D          

 34 38  0  0  0  0            999 V2000
   -1.1901   -3.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098   -2.3529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -2.2077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266   -1.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069   -1.1414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -1.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.8509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -1.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228   -0.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -1.5084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168   -2.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -2.7639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -2.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4850   -3.0585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705   -2.4028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -3.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -3.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -2.6932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -2.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5510   -3.6551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1776   -3.3919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939   -0.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1111   -0.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9830   -0.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4893    0.5584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2600    1.3509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9429    1.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9697    2.6384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5942    1.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3139    0.5316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3867    1.5368    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  1  0  0  0  0
  6  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
 11 12  1  0  0  0  0
 11 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
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  6 21  1  0  0  0  0
 21 22  1  0  0  0  0
  3 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 32 34  1  0  0  0  0
M  END

     RDKit          3D

 82 86  0  0  0  0  0  0  0  0999 V2000
   -7.8757   -0.3849   -0.5532 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7879   -0.8651    0.1692 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5536   -0.4971   -0.4224 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.7919   -1.7339   -0.7199 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3099   -1.6524   -0.5826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7946   -0.2241   -0.7177 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3656    0.2923   -2.0486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3209   -0.1572   -0.7594 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6025   -1.4540   -0.8933 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8452   -1.3957   -0.4338 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4832   -0.0739   -0.6482 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4837    0.2922   -2.1458 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8979   -0.0018   -0.2157 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6553   -1.2734   -0.0607 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2391   -2.2366    0.9777 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1263   -1.2038   -0.2491 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9505   -0.3302    0.6060 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.3616   -0.4334    0.1123 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8190    0.7435   -0.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1823    1.0828   -0.7058 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7791    1.7198    0.0853 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8444    2.9592   -0.0736 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6973    1.0327    0.5477 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9334    0.8240    1.0542 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4789    0.8984    1.4859 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7399    0.9646    0.1416 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8470    2.3567   -0.3801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6827    0.5716    0.3804 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2960    0.8486    1.5207 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7032    0.4185    1.7034 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4196    0.6112    0.3790 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8824    0.4175    0.5609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6058    1.7681    0.4052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2611   -0.0665    1.9425 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8544   -0.8012   -1.6026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8180   -0.7175   -0.1071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9110    0.7117   -0.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8501    0.0873   -1.3166 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1015   -2.1434   -1.7259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1404   -2.5425   -0.0100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8691   -2.2285   -1.4350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9637   -2.1211    0.3574 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4985    0.5488   -2.7330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8770    1.2675   -1.9214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9255   -0.4640   -2.5949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0223    0.4451   -1.6733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0662   -2.3014   -0.3567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5674   -1.7378   -1.9714 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8565   -1.6360    0.6399 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4217   -2.1705   -0.9792 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1070    1.3178   -2.3184 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9224   -0.4876   -2.7107 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5097    0.2699   -2.5692 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4802    0.6055   -0.9762 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3403   -1.8476   -1.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2218   -2.6758    1.3915 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7941   -1.8032    1.9003 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6988   -3.1337    0.6743 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5223   -2.2597   -0.1228 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3339   -0.8918   -1.3199 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0214   -0.6936    1.6704 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9411   -1.3593    0.0062 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5830    0.2724   -1.3505 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8964    1.2341    0.1308 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1719    2.0208   -1.3014 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4975    0.3892    1.8731 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2013    1.8640    0.7959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1826   -0.0337    2.0008 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2447    1.7460    2.1192 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0387    2.5696   -1.1310 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7902    3.0963    0.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8121    2.5622   -0.8820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7455    1.3877    2.2952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6630   -0.6485    2.0010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2018    1.0581    2.4421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2374    1.6692    0.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7768    2.0089   -0.6544 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5271    1.7654    1.0214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9021    2.5083    0.8822 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6614   -0.8926    2.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3220   -0.3896    1.9671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1985    0.7576    2.7047 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  1  6
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  6
 11 13  1  0
 13 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  6
 26 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 32 34  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 23  1  0
 23 21  1  0
 21 22  2  0
 21 19  1  0
 19 20  1  0
 19 18  2  0
 32  3  1  0
 18 17  1  0
 31  6  1  0
 28  8  1  0
 26 11  1  0
  1 35  1  0
  1 36  1  0
  1 37  1  0
  3 38  1  6
  4 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  7 43  1  0
  7 44  1  0
  7 45  1  0
  8 46  1  6
  9 47  1  0
  9 48  1  0
 10 49  1  0
 10 50  1  0
 12 51  1  0
 12 52  1  0
 12 53  1  0
 13 54  1  6
 24 66  1  0
 24 67  1  0
 25 68  1  0
 25 69  1  0
 27 70  1  0
 27 71  1  0
 27 72  1  0
 29 73  1  0
 30 74  1  0
 30 75  1  0
 31 76  1  6
 33 77  1  0
 33 78  1  0
 33 79  1  0
 34 80  1  0
 34 81  1  0
 34 82  1  0
 14 55  1  6
 15 56  1  0
 15 57  1  0
 15 58  1  0
 16 59  1  0
 16 60  1  0
 17 61  1  1
 20 63  1  0
 20 64  1  0
 20 65  1  0
 18 62  1  0
M  END


  Mrv1533004201501372D          

 34 38  0  0  0  0            999 V2000
   -1.1901   -3.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9098   -2.3529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0976   -2.2077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1827   -1.4318    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9948   -1.2866    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5266   -1.9173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8069   -1.1414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3387   -1.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6190   -0.9961    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4311   -0.8509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9629   -1.4816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3228   -0.7393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7875   -1.5084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0168   -2.3009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3340   -2.7639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6826   -2.2576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4850   -3.0585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8705   -2.4028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5902   -3.1787    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -3.3239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2463   -2.6932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4342   -2.8384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5510   -3.6551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1776   -3.3919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2939   -0.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1111   -0.9700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9830   -0.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4893    0.5584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2600    1.3509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9429    1.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9697    2.6384    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5942    1.3075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3139    0.5316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3867    1.5368    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  1  0  0  0  0
  6  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
 11 12  1  0  0  0  0
 11 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
 11 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  6 21  1  0  0  0  0
 21 22  1  0  0  0  0
  3 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 13 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 32 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0326711

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1CCC2(C)C3CCC4(C)C(CCC4(C)C3=CCC2C1(C)C)C(C)CC1OC(=O)C(C)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C31H48O3/c1-19(17-21-18-20(2)27(32)34-21)22-11-15-31(7)24-9-10-25-28(3,4)26(33-8)13-14-29(25,5)23(24)12-16-30(22,31)6/h9,18-19,21-23,25-26H,10-17H2,1-8H3

> <INCHI_KEY>
RHCAOVDBFCREAC-UHFFFAOYSA-N

> <FORMULA>
C31H48O3

> <MOLECULAR_WEIGHT>
468.722

> <EXACT_MASS>
468.360345406

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
57.09039285452239

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-(2-{5-methoxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-14-yl}propyl)-3-methyl-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
7.20

> <JCHEM_LOGP>
7.252142839333334

> <ALOGPS_LOGS>
-7.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.600548750330745

> <JCHEM_PKA_STRONGEST_BASIC>
-4.125634347619257

> <JCHEM_POLAR_SURFACE_AREA>
35.53

> <JCHEM_REFRACTIVITY>
139.30299999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.59e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(2-{5-methoxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-14-yl}propyl)-3-methyl-5H-furan-2-one

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  C   UNK     0      -2.221  -5.841   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.698  -4.392   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -0.182  -4.121   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.341  -2.673   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.857  -2.402   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.850  -3.579   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.373  -2.131   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.366  -3.308   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.889  -1.859   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.405  -1.588   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.398  -2.766   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.069  -1.380   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.937  -2.816   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.365  -4.295   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.090  -5.159   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.874  -4.214   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.505  -5.709   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.358  -4.485   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.835  -5.934   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.319  -6.205   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.326  -5.027   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.810  -5.298   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.028  -6.823   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.332  -6.332   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.882  -1.600   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.407  -1.811   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.302  -0.173   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      10.247   1.042   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       9.819   2.522   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      11.093   3.386   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      11.143   4.925   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      12.309   2.441   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.786   0.992   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.788   2.869   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   21                                             
CONECT    7    6                                                            
CONECT    8    6    9   18                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   16                                             
CONECT   12   11                                                            
CONECT   13   11   14   25                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17   18                                             
CONECT   17   16                                                            
CONECT   18   16    8   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    6   22                                                  
CONECT   22   21    3   23   24                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   13   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32   28                                                       
CONECT   34   32                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   76    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₄₈O₃

Average Mass

468.7220 Da

Monoisotopic Mass

468.36035 Da

IUPAC Name

5-(2-{5-methoxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-14-yl}propyl)-3-methyl-2,5-dihydrofuran-2-one

Traditional Name

5-(2-{5-methoxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-9-en-14-yl}propyl)-3-methyl-5H-furan-2-one

CAS Registry Number

Not Available

SMILES

COC1CCC2(C)C3CCC4(C)C(CCC4(C)C3=CCC2C1(C)C)C(C)CC1OC(=O)C(C)=C1

InChI Identifier

InChI=1S/C31H48O3/c1-19(17-21-18-20(2)27(32)34-21)22-11-15-31(7)24-9-10-25-28(3,4)26(33-8)13-14-29(25,5)23(24)12-16-30(22,31)6/h9,18-19,21-23,25-26H,10-17H2,1-8H3

InChI Key

RHCAOVDBFCREAC-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
Abies mariesii	LOTUS Database	35616633
Abies sibirica	LOTUS Database	35616633
Abies veitchii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as withanolides and derivatives. These are c28 steroids structurally characterized by an ergostane skeleton usually functionalized at carbons 1, 22 and 26 to form a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Withanolides and derivatives

Alternative Parents

Substituents

Triterpenoid
Withanolide-skeleton
Delta-7-steroid
2-furanone
Dihydrofuran
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Lactone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	7.2	ALOGPS
logP	7.25	ChemAxon
logS	-7	ALOGPS
pKa (Strongest Acidic)	13.6	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	35.53 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	139.3 m³·mol⁻¹	ChemAxon
Polarizability	57.09 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

634545

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one (NP0326711)

MOL for NP0326711 (5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one)

3D MOL for NP0326711 (5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one)

3D SDF for NP0326711 (5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one)

3D-SDF for NP0326711 (5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one)

PDB for NP0326711 (5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one)

3D PDB for NP0326711 (5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one)

SMILES for NP0326711 (5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one)

INCHI for NP0326711 (5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one)

Structure for NP0326711 (5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one)

3D Structure for NP0326711 (5-(2-{7-methoxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}propyl)-3-methyl-5h-furan-2-one)