NP-MRD: Showing NP-Card for (1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione (NP0231579)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-06 12:30:37 UTC

Updated at

2022-09-06 12:30:37 UTC

NP-MRD ID

NP0231579

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione

Description

11079-53-1 Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. (1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione is found in Hypericum perforatum. Based on a literature review very few articles have been published on 11079-53-1.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062214302D          

 39 40  0  0  1  0            999 V2000
   -1.2360    3.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4180    3.0191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0842    3.6736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1023    2.2569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6045    1.6024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    0.8402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5291    0.7325    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4214    1.5504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2134   -0.0297    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6116   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0241   -0.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8491   -0.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2616   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2616   -1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5291   -0.7919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2913   -1.1076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2913   -1.9326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5769   -2.3451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -1.9326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8521   -2.3451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -1.1076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0219   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3544    0.4552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2913    1.0482    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2913    1.8732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5769    2.2857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0058    2.2857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0058    3.1107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7203    1.8732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0535    0.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6369    1.3159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3692   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1942   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6067   -0.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4317   -0.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8442   -1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8442   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0535   -0.7919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6369   -1.3753    0.0000 O   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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 32 38  2  0  0  0  0
 16 38  1  0  0  0  0
 38 39  1  0  0  0  0
M  END

     RDKit          3D

 91 92  0  0  0  0  0  0  0  0999 V2000
    5.7798   -2.8382    0.6646 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2019   -1.9402   -0.3659 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1053   -1.1496   -1.2293 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8898   -1.8355   -0.5284 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3149   -0.9783   -1.5124 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4048    0.1337   -1.3157 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0823    0.0513   -0.7016 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3072   -0.9585   -1.6265 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3627    1.3572   -0.8835 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5117    2.0126   -2.2225 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1277    3.3652   -2.2574 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5878    4.4484   -2.5086 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0545    4.3725   -2.7672 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0429    5.7967   -2.5413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1204    1.2376   -0.5933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4082    0.6778    0.7873 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2253    1.6593    1.5989 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5466    1.9326    1.0735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6263    1.8890    1.8195 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5391    1.5568    3.2510 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9459    2.1738    1.2114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0732    0.5856    1.4220 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1672    1.2345    2.4007 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9083   -0.3649    0.7398 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0895   -0.1776    1.5995 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0554    0.3775    1.1008 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2588   -0.5668    3.0097 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2307   -2.0514    3.2310 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6142   -0.0735    3.5621 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2307   -1.6510    0.7307 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7587   -2.7970    0.8576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2496   -1.7131    0.5550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8276   -3.0363    0.2449 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2797   -3.1203    0.1157 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8827   -3.4151   -1.0125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1142   -3.6861   -2.2423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3655   -3.4819   -1.0983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0099   -0.6531    0.6660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4060   -0.7187    0.6758 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6894   -3.3086    0.1909 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1304   -2.3072    1.5616 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0493   -3.6233    0.9865 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1789   -1.3518   -0.9837 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0019   -1.3904   -2.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8490   -0.0777   -1.1079 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2968   -2.4426    0.1328 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1587   -0.5630   -2.1920 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8451   -1.6977   -2.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9046    1.0974   -1.0233 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1285    0.4342   -2.4270 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3972   -1.9693   -1.2598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7211   -0.6859   -1.7898 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7733   -0.9040   -2.6668 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7473    2.0777   -0.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5788    2.2155   -2.4845 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0897    1.4411   -3.0704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1752    3.4963   -2.0885 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4566    5.3709   -3.0344 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6192    3.8845   -1.9591 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1554    3.7342   -3.6956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0185    6.2270   -1.5181 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5367    6.4368   -3.2533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0733    5.6827   -2.9421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7469    0.8445   -1.3837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4434    2.3281   -0.5063 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3386    1.1828    2.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5904    2.5547    1.7580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6262    2.1827    0.0123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5034    1.7748    3.7747 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3037    0.5120    3.4371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7248    2.1878    3.6993 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8588    2.2915    0.1117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3901    3.1269    1.6109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6986    1.3791    1.4196 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5326   -0.0449    3.6860 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7631   -2.1972    4.2342 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2031   -2.4136    3.4343 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8276   -2.6247    2.5330 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5809    0.0574    4.6514 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7941    0.9040    3.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4392   -0.7369    3.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2986   -3.4504   -0.6655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4682   -3.7373    1.0610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9015   -2.9660    0.9864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7008   -2.7311   -2.6366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2930   -4.4022   -2.0933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7532   -4.0877   -3.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7374   -4.0046   -1.9877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8340   -2.4856   -0.9375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7046   -4.0944   -0.2141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9484   -0.7809    1.5026 H   0  0  0  0  0  0  0  0  0  0  0  0
 28 27  1  0
 27 29  1  0
 27 25  1  0
 25 26  2  0
 24 25  1  1
 24 30  1  0
 30 31  2  0
 30 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  2  3
 35 36  1  0
 35 37  1  0
 32 38  2  0
 38 39  1  0
 38 16  1  0
 16 17  1  1
 17 18  1  0
 18 19  2  3
 19 20  1  0
 19 21  1  0
 16 15  1  0
 15  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  3
 12 13  1  0
 12 14  1  0
  9  7  1  0
  7  8  1  6
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
 16 22  1  0
 22 23  2  0
  7 24  1  0
 22 24  1  0
 28 76  1  0
 28 77  1  0
 28 78  1  0
 27 75  1  0
 29 79  1  0
 29 80  1  0
 29 81  1  0
 33 82  1  0
 33 83  1  0
 34 84  1  0
 36 85  1  0
 36 86  1  0
 36 87  1  0
 37 88  1  0
 37 89  1  0
 37 90  1  0
 39 91  1  0
 17 66  1  0
 17 67  1  0
 18 68  1  0
 20 69  1  0
 20 70  1  0
 20 71  1  0
 21 72  1  0
 21 73  1  0
 21 74  1  0
 15 64  1  0
 15 65  1  0
  9 54  1  1
 10 55  1  0
 10 56  1  0
 11 57  1  0
 13 58  1  0
 13 59  1  0
 13 60  1  0
 14 61  1  0
 14 62  1  0
 14 63  1  0
  8 51  1  0
  8 52  1  0
  8 53  1  0
  6 49  1  0
  6 50  1  0
  5 47  1  0
  5 48  1  0
  4 46  1  0
  1 40  1  0
  1 41  1  0
  1 42  1  0
  3 43  1  0
  3 44  1  0
  3 45  1  0
M  END


  Mrv1652309062214302D          

 39 40  0  0  1  0            999 V2000
   -1.2360    3.1268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4180    3.0191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0842    3.6736    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1023    2.2569    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6045    1.6024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    0.8402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5291    0.7325    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4214    1.5504    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2134   -0.0297    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.6116   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0241   -0.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8491   -0.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2616   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2616   -1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5291   -0.7919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2913   -1.1076    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2913   -1.9326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5769   -2.3451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -1.9326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8521   -2.3451    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1376   -1.1076    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0219   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3544    0.4552    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2913    1.0482    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2913    1.8732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5769    2.2857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0058    2.2857    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0058    3.1107    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7203    1.8732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0535    0.7325    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6369    1.3159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3692   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1942   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6067   -0.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4317   -0.7442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8442   -1.4586    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8442   -0.0297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0535   -0.7919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6369   -1.3753    0.0000 O   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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  6  0  0  0
  7  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 35 37  1  0  0  0  0
 32 38  2  0  0  0  0
 16 38  1  0  0  0  0
 38 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0231579

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)[C@]12C(=O)C(CC=C(C)C)=C(O)[C@](CC=C(C)C)(C[C@H](CC=C(C)C)[C@@]1(C)CCC=C(C)C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H52O4/c1-22(2)13-12-19-33(11)27(16-14-23(3)4)21-34(20-18-25(7)8)30(37)28(17-15-24(5)6)31(38)35(33,32(34)39)29(36)26(9)10/h13-15,18,26-27,37H,12,16-17,19-21H2,1-11H3/t27-,33+,34-,35+/m0/s1

> <INCHI_KEY>
KGSZHKRKHXOAMG-IIFCFJOHSA-N

> <FORMULA>
C35H52O4

> <MOLECULAR_WEIGHT>
536.797

> <EXACT_MASS>
536.386560154

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
91

> <JCHEM_AVERAGE_POLARIZABILITY>
63.645276514715945

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,5S,7S,8R)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione

> <JCHEM_LOGP>
9.666358571

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
19.344345466304535

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.674655635201598

> <JCHEM_PKA_STRONGEST_BASIC>
-7.065784167207119

> <JCHEM_POLAR_SURFACE_AREA>
71.44

> <JCHEM_REFRACTIVITY>
166.68250000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,5S,7S,8R)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.307   5.837   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.780   5.636   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.157   6.857   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.191   4.213   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.128   2.991   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.539   1.568   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.988   1.367   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.787   2.894   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.398  -0.055   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.142  -0.055   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.912  -1.389   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.452  -1.389   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.222  -0.055   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.222  -2.723   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.988  -1.478   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.410  -2.068   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.410  -3.608   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.077  -4.378   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.257  -3.608   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.591  -4.378   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.257  -2.068   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.907  -0.055   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.662   0.850   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.410   1.957   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.410   3.497   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.077   4.267   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.744   4.267   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.744   5.807   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.078   3.497   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.833   1.367   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.922   2.456   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.423  -0.055   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.963  -0.055   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.733  -1.389   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.273  -1.389   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       9.043  -2.723   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       9.043  -0.055   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       3.833  -1.478   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       4.922  -2.567   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   24                                             
CONECT    8    7                                                            
CONECT    9    7   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    9   16                                                       
CONECT   16   15   17   22   38                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   16   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    7   25   30                                             
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   24   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   38                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
CONECT   38   32   16   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₂O₄

Average Mass

536.7970 Da

Monoisotopic Mass

536.38656 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)[C@]12C(=O)C(CC=C(C)C)=C(O)[C@](CC=C(C)C)(C[C@H](CC=C(C)C)[C@@]1(C)CCC=C(C)C)C2=O

InChI Identifier

InChI=1S/C35H52O4/c1-22(2)13-12-19-33(11)27(16-14-23(3)4)21-34(20-18-25(7)8)30(37)28(17-15-24(5)6)31(38)35(33,32(34)39)29(36)26(9)10/h13-15,18,26-27,37H,12,16-17,19-21H2,1-11H3/t27-,33+,34-,35+/m0/s1

InChI Key

KGSZHKRKHXOAMG-IIFCFJOHSA-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
Hypericum perforatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Bicyclic monoterpenoids

Alternative Parents

Substituents

Bicyclic monoterpenoid
Cyclohexenone
Vinylogous acid
Ketone
Enol
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	9.67	ChemAxon
pKa (Strongest Acidic)	4.67	ChemAxon
pKa (Strongest Basic)	-7.1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	71.44 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	166.68 m³·mol⁻¹	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00034542

Chemspider ID

8112650

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9937023

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione (NP0231579)

MOL for NP0231579 ((1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D MOL for NP0231579 ((1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D SDF for NP0231579 ((1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D-SDF for NP0231579 ((1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione)

PDB for NP0231579 ((1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D PDB for NP0231579 ((1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione)

SMILES for NP0231579 ((1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione)

INCHI for NP0231579 ((1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione)

Structure for NP0231579 ((1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione)

3D Structure for NP0231579 ((1s,5s,7s,8r)-4-hydroxy-8-methyl-3,5,7-tris(3-methylbut-2-en-1-yl)-8-(4-methylpent-3-en-1-yl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione)