NP-MRD: Showing NP-Card for (2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid (NP0240907)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 00:50:30 UTC

Updated at

2022-09-07 00:50:30 UTC

NP-MRD ID

NP0240907

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid

Description

CHEMBL508565 belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid is found in Saussurea muliensis. Based on a literature review very few articles have been published on CHEMBL508565.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072202502D          

 43 48  0  0  1  0            999 V2000
    5.9337    1.9394    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
    6.8522    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -4.5888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  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
    4.8395    0.4125    0.0000 C   0  0  1  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
    5.2520    1.1270    0.0000 C   0  0  1  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
    4.0145    0.4125    0.0000 C   0  0  2  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
    2.7770   -0.3020    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
    1.5395    0.4125    0.0000 C   0  0  2  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  1  0  0  0  0  0  0  0  0  0
    0.4452   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -1.3966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1053   -0.0538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   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
    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
    2.7770    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6907    1.9475    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
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
  4 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 30 29  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  1  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 32 37  1  0  0  0  0
 37 38  1  0  0  0  0
 39 38  1  6  0  0  0
 30 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 29 42  1  0  0  0  0
 24 42  1  0  0  0  0
 42 43  1  6  0  0  0
M  END

     RDKit          3D

 95100  0  0  0  0  0  0  0  0999 V2000
    3.1122   -0.3762   -1.8856 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5170    0.4725   -0.7504 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0407    1.8490   -0.9089 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1134   -0.1008    0.5272 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3930   -0.6516    0.2287 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5461   -0.1400    0.8024 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4218    0.8284    1.5960 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8724   -0.6746    0.5239 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9457   -0.1757    1.0763 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3109   -0.6728    0.8341 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3867   -0.0672    1.4736 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6624   -0.5232    1.2549 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9489   -1.5769    0.4143 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2484   -2.0309    0.2004 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8782   -2.1713   -0.2153 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5828   -1.7234   -0.0058 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2436   -1.2078    0.9965 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8470   -0.8376    1.3392 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3572    0.3971    0.5504 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6653    1.5674    1.3926 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0434    0.3052   -0.7832 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3892    1.0594   -1.8933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0871    0.7333   -1.9966 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7746    0.9808   -0.6716 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7054    2.4607   -0.4250 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1214    0.1164    0.3379 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8374   -0.0561    1.6323 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2611    0.3121    1.5563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9458    0.6076    0.4821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3704    0.9534    0.6135 C   0  0  2  0  0  0  0  0  0  0  0  0
   -6.2090    0.0150    1.4174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9011   -1.0852    0.7196 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.2155   -2.4281    0.8379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2503   -1.3261    1.3696 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5881   -0.6218    2.3383 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1082   -2.3044    0.9132 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2402   -0.7749   -0.7167 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4284    0.7172   -0.7969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0707    1.3586   -0.6203 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.3287    1.1997   -1.9006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8985    1.6698   -1.6557 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2193    0.5941   -0.8398 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4232   -0.7568   -1.4396 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5123   -1.3381   -1.5054 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3509   -0.6480   -2.6424 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9302    0.1365   -2.3929 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4982    2.2341    0.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3473    2.6162   -1.2300 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9086    1.8917   -1.6345 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2681    0.7200    1.2345 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9344   -1.4921   -0.1513 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8044    0.6653    1.7604 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1533    0.7643    2.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.4708   -0.0181    1.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5733   -2.7532    0.8272 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0639   -3.0134   -0.8923 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7634   -2.2068   -0.5112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3234   -2.0407    0.2542 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7147   -1.6304    1.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7463   -0.6302    2.4388 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2036   -1.7213    1.1530 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2342    1.3162    2.3424 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2680    2.3641    0.9294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2426    2.0883    1.8226 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8776   -0.7867   -1.0699 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8383    0.6897   -2.8520 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4930    2.1314   -1.8941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5026    1.3929   -2.8121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1606   -0.2868   -2.3711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3095    2.8163    0.4091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6612    2.8582   -0.3889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0835    2.9383   -1.3810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0835   -0.9198   -0.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7080   -1.1128    1.9680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4039    0.5415    2.4649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7802    0.3333    2.5345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3313    1.8960    1.2754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6738   -0.3318    2.3535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0278    0.6614    1.8755 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6525   -3.1013    1.5765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1391   -2.3389    1.0727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2912   -2.9224   -0.1522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8633   -3.0230    0.2422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4739   -1.1093   -1.4225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1818   -1.3074   -1.0265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0489    1.0891    0.0705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8708    1.0390   -1.7604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3286    2.4729   -0.5741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7169    1.9513   -2.6608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4067    0.2449   -2.4083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0460    2.6077   -1.0414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4658    1.8586   -2.6325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5157   -1.4263   -1.3958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6627   -0.7296   -2.5257 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1881   -1.3453   -0.8918 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  1
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  1
 24 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 32 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  6
 32 34  1  1
 34 36  1  0
 34 35  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 13 15  1  0
 15 16  2  0
 21  2  1  0
 42 24  1  0
 16 10  1  0
 26 19  1  0
 42 29  1  0
 39 30  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  3 47  1  0
  3 48  1  0
  3 49  1  0
  4 50  1  1
 17 58  1  0
 17 59  1  0
 18 60  1  0
 18 61  1  0
 20 62  1  0
 20 63  1  0
 20 64  1  0
 21 65  1  6
 22 66  1  0
 22 67  1  0
 23 68  1  0
 23 69  1  0
 25 70  1  0
 25 71  1  0
 25 72  1  0
 26 73  1  6
 27 74  1  0
 27 75  1  0
 28 76  1  0
 30 77  1  1
 31 78  1  0
 31 79  1  0
 33 80  1  0
 33 81  1  0
 33 82  1  0
 37 84  1  0
 37 85  1  0
 38 86  1  0
 38 87  1  0
 39 88  1  1
 40 89  1  0
 40 90  1  0
 41 91  1  0
 41 92  1  0
 43 93  1  0
 43 94  1  0
 43 95  1  0
 36 83  1  0
  8 51  1  0
  9 52  1  0
 11 53  1  0
 12 54  1  0
 14 55  1  0
 15 56  1  0
 16 57  1  0
M  END


  Mrv1652309072202502D          

 43 48  0  0  1  0            999 V2000
    5.9337    1.9394    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
    6.8522    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.3145    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5520   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7270   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3145   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -4.5888    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -3.1599    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4895   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -0.3020    0.0000 C   0  0  0  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
    4.8395    0.4125    0.0000 C   0  0  1  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
    5.2520    1.1270    0.0000 C   0  0  1  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
    4.0145    0.4125    0.0000 C   0  0  2  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
    2.7770   -0.3020    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
    1.5395    0.4125    0.0000 C   0  0  2  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  1  0  0  0  0  0  0  0  0  0
    0.4452   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6165   -1.3966    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1053   -0.0538    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   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
    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
    2.7770    1.1270    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6907    1.9475    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
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 10 16  1  0  0  0  0
  4 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
  2 21  1  0  0  0  0
 21 22  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 19 26  1  0  0  0  0
 26 27  1  1  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 30 29  1  6  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  1  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 32 37  1  0  0  0  0
 37 38  1  0  0  0  0
 39 38  1  6  0  0  0
 30 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 29 42  1  0  0  0  0
 24 42  1  0  0  0  0
 42 43  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0240907

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)[C@@H](CC[C@@]2(C)[C@H]1CC[C@]1(C)[C@@H]2CC=C2[C@@H]3C[C@](C)(CC[C@@H]3CC[C@@]12C)C(O)=O)OC(=O)\C=C\C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C38H52O5/c1-34(2)29-17-22-38(6)30(13-12-28-27-23-35(3,33(41)42)19-15-25(27)16-21-37(28,38)5)36(29,4)20-18-31(34)43-32(40)14-9-24-7-10-26(39)11-8-24/h7-12,14,25,27,29-31,39H,13,15-23H2,1-6H3,(H,41,42)/b14-9+/t25-,27-,29+,30-,31-,35+,36+,37-,38-/m1/s1

> <INCHI_KEY>
OWOGADCAJRSRCM-NNRMRRARSA-N

> <FORMULA>
C38H52O5

> <MOLECULAR_WEIGHT>
588.829

> <EXACT_MASS>
588.381474774

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
95

> <JCHEM_AVERAGE_POLARIZABILITY>
69.47768657226433

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,4aS,6aS,6bR,8aR,10R,12aR,12bR,14bR)-10-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-2-carboxylic acid

> <JCHEM_LOGP>
9.025111709666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.39862098607515

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.581652800169311

> <JCHEM_PKA_STRONGEST_BASIC>
-5.9547318749588785

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
170.69800000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4aS,6aS,6bR,8aR,10R,12aR,12bR,14bR)-10-{[(2E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1H-picene-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      11.076   3.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.344   2.104   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.791   2.630   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.114   0.770   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      13.654   0.770   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      14.424  -0.564   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      15.964  -0.564   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      13.654  -1.897   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.424  -3.231   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.654  -4.565   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.424  -5.898   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.654  -7.232   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.114  -7.232   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      11.344  -8.566   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      11.344  -5.898   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.114  -4.565   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.344  -0.564   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.264  -0.564   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.034   3.437   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.494   3.437   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.831  -2.080   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.883  -1.090   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -1.151  -2.607   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -2.063  -0.100   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.023   3.635   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4   21                                             
CONECT    3    2                                                            
CONECT    4    2    5   17                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   10                                                       
CONECT   17    4   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21   26                                             
CONECT   20   19                                                            
CONECT   21   19    2   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   42                                             
CONECT   25   24                                                            
CONECT   26   24   19   27                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   42                                                  
CONECT   30   29   31   39                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33   34   37                                             
CONECT   33   32                                                            
CONECT   34   32   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   32   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   30   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   29   24   43                                             
CONECT   43   42                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   96    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₈H₅₂O₅

Average Mass

588.8290 Da

Monoisotopic Mass

588.38147 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC1(C)[C@@H](CC[C@@]2(C)[C@H]1CC[C@]1(C)[C@@H]2CC=C2[C@@H]3C[C@](C)(CC[C@@H]3CC[C@@]12C)C(O)=O)OC(=O)\C=C\C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C38H52O5/c1-34(2)29-17-22-38(6)30(13-12-28-27-23-35(3,33(41)42)19-15-25(27)16-21-37(28,38)5)36(29,4)20-18-31(34)43-32(40)14-9-24-7-10-26(39)11-8-24/h7-12,14,25,27,29-31,39H,13,15-23H2,1-6H3,(H,41,42)/b14-9+/t25-,27-,29+,30-,31-,35+,36+,37-,38-/m1/s1

InChI Key

OWOGADCAJRSRCM-NNRMRRARSA-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
Saussurea muliensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Coumaric acid ester
Cinnamic acid or derivatives
Coumaric acid or derivatives
Cinnamic acid ester
Hydroxycinnamic acid or derivatives
Styrene
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acid ester
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Dicarboxylic acid or derivatives
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Carboxylic acid
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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

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

24713105

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44577083

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid (NP0240907)

MOL for NP0240907 ((2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid)

3D MOL for NP0240907 ((2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid)

3D SDF for NP0240907 ((2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid)

3D-SDF for NP0240907 ((2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid)

PDB for NP0240907 ((2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid)

3D PDB for NP0240907 ((2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid)

SMILES for NP0240907 ((2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid)

INCHI for NP0240907 ((2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid)

Structure for NP0240907 ((2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid)

3D Structure for NP0240907 ((2s,4as,6as,6br,8ar,10r,12ar,12br,14br)-10-{[(2e)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy}-2,6a,6b,9,9,12a-hexamethyl-3,4,4a,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid)