NP-MRD: Showing NP-Card for [(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate (NP0204385)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 00:02:57 UTC

Updated at

2022-09-05 00:02:58 UTC

NP-MRD ID

NP0204385

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate

Description

Isokarounidiol diacetate belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups. [(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate is found in Cucurbita moschata and Trichosanthes cucumeroides. Based on a literature review very few articles have been published on Isokarounidiol diacetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052202022D          

 38 42  0  0  1  0            999 V2000
    7.9140   -2.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7707   -1.6788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4027   -1.1485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9955   -1.3966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8522   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9337   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  6  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  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  1  0  0  0
  6 23  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 24 36  1  0  0  0  0
 36 37  1  6  0  0  0
 37 38  2  0  0  0  0
 16 38  1  0  0  0  0
M  END

     RDKit          3D

 90 94  0  0  0  0  0  0  0  0999 V2000
   -9.3007    2.1096    1.3616 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8450    2.2733    0.9826 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5403    3.0662    0.0677 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9030    1.5694    1.6297 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5580    1.4376    1.5676 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9714    0.7615    0.3712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2862    1.5005   -0.8928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4883   -0.6668    0.3251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4244   -1.6651    0.6154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2380   -1.5355   -0.3567 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.8378   -1.8279   -1.7236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2874   -2.6172   -0.0009 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8741   -2.4496   -0.3977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4562   -1.0382   -0.7209 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6015   -0.8252   -2.2106 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9964   -0.8960   -0.4381 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5330    0.3036   -0.1743 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7410    1.4443    0.3332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7265    1.3243   -0.0641 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2349   -0.0797    0.1169 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0307   -0.4376    1.5679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6895   -0.1352   -0.2877 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4660    0.7956    0.5727 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9922    0.5260   -0.4007 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1414    0.7810   -1.8823 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5043    1.7349    0.3259 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8233    1.4692    1.0211 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7613    0.6693    0.1370 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9748    0.5251    0.8909 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1607    1.1415    0.5045 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4215    0.9915    1.2878 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0995    1.8366   -0.5533 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1976   -0.6545   -0.2425 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5078   -1.0949   -1.6332 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8316   -1.6891    0.7015 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7152   -0.6710    0.0837 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1076   -1.9771   -0.2116 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8236   -2.0914   -0.4583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4830    2.5254    2.3720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9427    2.5917    0.5957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5084    1.0181    1.3579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1479    0.9645    2.5276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1292    2.5154    1.5735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2606    1.2838   -1.3394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5355    1.1481   -1.6764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1006    2.5828   -0.7359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0111   -0.8744   -0.6347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2784   -0.8075    1.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8587   -2.6797    0.3735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1224   -1.7080    1.6575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8734   -2.1794   -1.6914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7126   -0.9717   -2.4157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2471   -2.6521   -2.1720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4150   -2.8929    1.0880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6596   -3.5552   -0.5180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5797   -3.0958   -1.2445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2519   -2.7977    0.4805 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3981   -0.7996   -2.7409 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0949    0.0979   -2.5008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1168   -1.6937   -2.6833 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1049    2.3834   -0.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8442    1.5238    1.4393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9426    1.7636   -1.0461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2422    1.9853    0.6959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9617   -0.7701    2.0752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2291   -1.1882    1.7262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7055    0.4516    2.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7328    0.2794   -1.3276 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1954    1.8469    0.2497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2393    0.7560    1.6410 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1558    1.0077   -2.2034 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6432   -0.0107   -2.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5383    1.7154   -2.0872 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7850    1.9967    1.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5736    2.6290   -0.3376 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7065    0.9959    2.0076 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3079    2.4663    1.2017 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0111    1.3224   -0.7206 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2460    1.0450    2.3775 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9688    0.0662    1.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0829    1.8452    0.9905 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6142   -1.3563   -2.2402 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1486   -0.3256   -2.1574 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1478   -2.0267   -1.6708 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2760   -1.6803    1.6688 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7564   -2.6853    0.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8736   -1.3994    0.8846 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7049   -0.5949    1.2181 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7403   -2.8860   -0.2286 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3768   -3.0852   -0.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  6  5  1  1
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  6
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  1
 20 22  1  0
 22 23  1  0
 17 24  1  0
 24 25  1  6
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
 28 33  1  0
 33 34  1  0
 33 35  1  0
 33 36  1  0
 36 37  1  0
 37 38  2  0
 23  6  1  0
 36 24  1  0
 22 10  1  0
 20 14  1  0
 38 16  1  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
  5 42  1  0
  5 43  1  0
  7 44  1  0
  7 45  1  0
  7 46  1  0
  8 47  1  0
  8 48  1  0
  9 49  1  0
  9 50  1  0
 11 51  1  0
 11 52  1  0
 11 53  1  0
 12 54  1  0
 12 55  1  0
 13 56  1  0
 13 57  1  0
 15 58  1  0
 15 59  1  0
 15 60  1  0
 18 61  1  0
 18 62  1  0
 19 63  1  0
 19 64  1  0
 21 65  1  0
 21 66  1  0
 21 67  1  0
 22 68  1  6
 23 69  1  0
 23 70  1  0
 25 71  1  0
 25 72  1  0
 25 73  1  0
 26 74  1  0
 26 75  1  0
 27 76  1  0
 27 77  1  0
 28 78  1  6
 31 79  1  0
 31 80  1  0
 31 81  1  0
 34 82  1  0
 34 83  1  0
 34 84  1  0
 35 85  1  0
 35 86  1  0
 35 87  1  0
 36 88  1  1
 37 89  1  0
 38 90  1  0
M  END


  Mrv1652309052202022D          

 38 42  0  0  1  0            999 V2000
    7.9140   -2.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7707   -1.6788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4027   -1.1485    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9955   -1.3966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8522   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9337   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9355    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9355    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4452    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  6  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  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  1  0  0  0
  6 23  1  0  0  0  0
 17 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 28 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 24 36  1  0  0  0  0
 36 37  1  6  0  0  0
 37 38  2  0  0  0  0
 16 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0204385

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC[C@]1(C)CC[C@]2(C)CC[C@]3(C)C4=C(CC[C@@]3(C)[C@@H]2C1)[C@@]1(C)CC[C@@H](OC(C)=O)C(C)(C)[C@@H]1C=C4

> <INCHI_IDENTIFIER>
InChI=1S/C34H52O4/c1-22(35)37-21-30(5)16-17-31(6)18-19-33(8)25-10-11-26-29(3,4)28(38-23(2)36)13-14-32(26,7)24(25)12-15-34(33,9)27(31)20-30/h10-11,26-28H,12-21H2,1-9H3/t26-,27+,28+,30+,31+,32+,33+,34-/m0/s1

> <INCHI_KEY>
BGGXREMBPKLZCX-HQQKMQDPSA-N

> <FORMULA>
C34H52O4

> <MOLECULAR_WEIGHT>
524.786

> <EXACT_MASS>
524.386560154

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
62.46521601441272

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R,4aS,6aS,8aR,10R,12aS,14aS,14bR)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,2,3,4,4a,5,6,6a,8a,9,10,11,12,12a,13,14,14a,14b-octadecahydropicen-2-yl]methyl acetate

> <JCHEM_LOGP>
6.599041016999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.698352992007849

> <JCHEM_POLAR_SURFACE_AREA>
52.6

> <JCHEM_REFRACTIVITY>
152.835

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,4aS,6aS,8aR,10R,12aS,14aS,14bR)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      14.773  -4.650   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      14.505  -3.134   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      15.685  -2.144   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      13.058  -2.607   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      12.791  -1.090   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.076  -2.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.574   3.437   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.034   3.437   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.494   3.437   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.264  -0.564   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.746   0.770   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -2.516   2.104   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.056   2.104   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -1.746   3.437   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.883   2.630   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       0.831   3.620   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   23                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   22                                             
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   20                                             
CONECT   15   14                                                            
CONECT   16   14   17   38                                                  
CONECT   17   16   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   14   21   22                                             
CONECT   21   20                                                            
CONECT   22   20   10   23                                                  
CONECT   23   22    6                                                       
CONECT   24   17   25   26   36                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   28   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33   24   37                                                  
CONECT   37   36   38                                                       
CONECT   38   37   16                                                       
MASTER        0    0    0    0    0    0    0    0   38    0   84    0
END

View in JSmol

Synonyms

Value	Source
Isokarounidiol diacetic acid	Generator

Chemical Formula

C₃₄H₅₂O₄

Average Mass

524.7860 Da

Monoisotopic Mass

524.38656 Da

IUPAC Name

[(2R,4aS,6aS,8aR,10R,12aS,14aS,14bR)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,2,3,4,4a,5,6,6a,8a,9,10,11,12,12a,13,14,14a,14b-octadecahydropicen-2-yl]methyl acetate

Traditional Name

[(2R,4aS,6aS,8aR,10R,12aS,14aS,14bR)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC[C@]1(C)CC[C@]2(C)CC[C@]3(C)C4=C(CC[C@@]3(C)[C@@H]2C1)[C@@]1(C)CC[C@@H](OC(C)=O)C(C)(C)[C@@H]1C=C4

InChI Identifier

InChI=1S/C34H52O4/c1-22(35)37-21-30(5)16-17-31(6)18-19-33(8)25-10-11-26-29(3,4)28(38-23(2)36)13-14-32(26,7)24(25)12-15-34(33,9)27(31)20-30/h10-11,26-28H,12-21H2,1-9H3/t26-,27+,28+,30+,31+,32+,33+,34-/m0/s1

InChI Key

BGGXREMBPKLZCX-HQQKMQDPSA-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
Cucurbita moschata	LOTUS Database	35616633
Trichosanthes cucumeroides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dicarboxylic acids and derivatives. These are organic compounds containing exactly two carboxylic acid groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Dicarboxylic acids and derivatives

Direct Parent

Dicarboxylic acids and derivatives

Alternative Parents

Substituents

Dicarboxylic acid or derivatives
Carboxylic acid ester
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	6.6	ChemAxon
pKa (Strongest Basic)	-6.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	152.84 m³·mol⁻¹	ChemAxon
Polarizability	62.47 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	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

8544998

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10369552

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate (NP0204385)

MOL for NP0204385 ([(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate)

3D MOL for NP0204385 ([(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate)

3D SDF for NP0204385 ([(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate)

3D-SDF for NP0204385 ([(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate)

PDB for NP0204385 ([(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate)

3D PDB for NP0204385 ([(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate)

SMILES for NP0204385 ([(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate)

INCHI for NP0204385 ([(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate)

Structure for NP0204385 ([(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate)

3D Structure for NP0204385 ([(2r,4as,6as,8ar,10r,12as,14as,14br)-10-(acetyloxy)-2,4a,6a,9,9,12a,14a-heptamethyl-1,3,4,5,6,8a,10,11,12,13,14,14b-dodecahydropicen-2-yl]methyl acetate)