NP-MRD: Showing NP-Card for (3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate (NP0147269)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 02:50:17 UTC

Updated at

2022-09-02 02:50:18 UTC

NP-MRD ID

NP0147269

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate

Description

3Beta-(Palmitoyloxy)oleanan-13-ol belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate is found in Pentaclethra eetveldeana. Based on a literature review very few articles have been published on 3beta-(Palmitoyloxy)oleanan-13-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022204502D          

 49 53  0  0  1  0            999 V2000
    4.2868  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -16.0875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -15.2625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.1473  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -16.0875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.5762  -15.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -16.5000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.1473  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -17.3250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.5762  -18.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -16.5000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.2907  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -17.3250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   20.7197  -16.9125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -17.7375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   21.4341  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4308  -16.9623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.9611  -17.8808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -18.5625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.7197  -19.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -17.7375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.9552  -18.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9956  -16.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6083  -16.1163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 36 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 34 41  1  0  0  0  0
 41 42  1  1  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 32 45  1  0  0  0  0
 27 45  1  0  0  0  0
 45 46  1  6  0  0  0
 24 47  1  0  0  0  0
 19 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
M  END

     RDKit          3D

131135  0  0  0  0  0  0  0  0999 V2000
   14.1356   -1.3838    2.7748 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9681   -0.6022    2.1208 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2047   -0.4490    0.6710 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2459    0.2647   -0.1732 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8723   -0.2393   -0.4139 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9541   -0.4452    0.7190 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5587   -0.8889    0.2694 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8820    0.0912   -0.6234 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4902   -0.4743   -0.9787 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8678    0.5434   -1.8774 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4753    0.1917   -2.3547 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9338    1.2546   -3.2482 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8355    2.6349   -2.7880 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0333    3.1586   -1.7185 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0878    2.8311   -0.3060 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7458    1.4881    0.1782 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6057    0.7244    0.7433 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4778    0.9486    0.0657 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0191   -0.2963    0.4853 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0191   -0.1836    1.6281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1634    0.6532    1.2946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7748    0.3105   -0.0781 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5470    1.4803   -0.9485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1864   -0.9905   -0.4713 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8606   -1.6802   -1.6276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3066   -1.9025   -1.2539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0189   -0.6159   -0.8618 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1400    0.1360   -2.1374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2547    0.0638    0.2034 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.9295    1.2808    0.7884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1588    0.7112    1.5234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0120    0.1408    0.3854 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9793    1.1772   -0.5909 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4240    0.0182    0.8060 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.6609   -0.3272    2.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0149    0.2840    2.6803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8879    1.7783    2.7934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4004   -0.2630    4.0441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9876   -0.1323    1.6071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4824   -1.2571    0.7335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2872   -0.8272   -0.0898 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.8488    0.0355   -1.2334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5912   -1.9673   -0.7293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3287   -1.4286   -1.4085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3777   -1.0271   -0.2796 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2403   -2.2477    0.5870 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2920   -1.0924   -0.5883 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6304   -2.5641   -0.2343 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9018   -0.8596   -1.9138 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0049   -1.3126    2.0660 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.4202   -0.9401    3.7385 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.8461   -2.4300    2.9646 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0609    0.4151    2.5819 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.0282   -1.0061    2.4608 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.2016    0.1050    0.5661 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.4728   -1.4573    0.2233 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.7776    0.4512   -1.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.2039    1.3450    0.2237 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4189    0.4468   -1.1990 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9958   -1.2023   -1.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9427    0.3809    1.4165 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3075   -1.3794    1.2736 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6781   -1.8762   -0.1964 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9599   -0.9625    1.2222 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4765    0.2106   -1.5503 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7739    1.0961   -0.1891 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9261   -0.6952   -0.0640 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6104   -1.4243   -1.5363 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8607    1.5553   -1.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5516    0.6279   -2.7719 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6838   -0.6989   -3.0919 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8100   -0.2568   -1.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5928    1.2046   -4.1923 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9510    0.8690   -3.6753 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4977    3.2282   -3.7435 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8970    3.1041   -2.7064 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0330    4.3133   -1.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9175    2.9440   -2.0262 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4562    3.5800    0.2611 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1276    3.0633    0.1099 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8694   -0.8471    0.9369 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5542    0.2890    2.4720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2272   -1.2189    1.9427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9083    0.4648    2.1260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8990    1.7129    1.3826 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8170    2.1843   -0.4974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5021    2.0951   -0.9150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2272    1.2783   -1.9706 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4605   -1.6743    0.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4006   -2.7133   -1.6626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6928   -1.2569   -2.6077 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3357   -2.6966   -0.5251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8186   -2.2647   -2.1819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3041    1.2105   -2.0923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2128    0.0306   -2.7802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9269   -0.2533   -2.8202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1897   -0.6386    1.1001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2662    1.8248    1.4553 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3099    1.9732    0.0230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6833    1.5649    1.9463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8560   -0.0727    2.2443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3508    1.9858   -0.1864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8764    1.0608    0.7237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8448   -1.4038    2.4489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8722   -0.0019    2.9358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1565    2.2776    1.8547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5854    2.1148    3.5904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8301    1.9998    3.0464 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5102   -0.3961    4.0252 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9657   -1.2692    4.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1509    0.4518    4.8567 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3464    0.7066    0.9953 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8937   -0.5439    2.1386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3293   -2.1885    1.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3074   -1.4505   -0.0050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1925    0.9303   -1.3080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8629    0.3857   -1.0290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8937   -0.5403   -2.1863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4339   -2.8491   -0.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2396   -2.2926   -1.6001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8859   -2.1507   -2.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7300   -0.5068   -1.9273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3246   -2.3218    1.1799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2461   -3.1615   -0.0743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0559   -2.3997    1.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0210   -2.9395    0.5562 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5612   -3.1506   -1.1897 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7091   -2.5725    0.0445 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2626    0.1739   -2.1094 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2971   -1.1605   -2.7877 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8325   -1.5004   -2.0178 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  6
 22 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  6
 27 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  6
 32 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 36 38  1  0
 36 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  6
 41 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  1
 24 47  1  0
 47 48  1  0
 47 49  1  0
 47 19  1  0
 29 22  1  0
 45 32  1  0
 45 27  1  0
 41 34  1  0
  1 50  1  0
  1 51  1  0
  1 52  1  0
  2 53  1  0
  2 54  1  0
  3 55  1  0
  3 56  1  0
  4 57  1  0
  4 58  1  0
  5 59  1  0
  5 60  1  0
  6 61  1  0
  6 62  1  0
  7 63  1  0
  7 64  1  0
  8 65  1  0
  8 66  1  0
  9 67  1  0
  9 68  1  0
 10 69  1  0
 10 70  1  0
 11 71  1  0
 11 72  1  0
 12 73  1  0
 12 74  1  0
 13 75  1  0
 13 76  1  0
 14 77  1  0
 14 78  1  0
 15 79  1  0
 15 80  1  0
 19 81  1  1
 20 82  1  0
 20 83  1  0
 21 84  1  0
 21 85  1  0
 23 86  1  0
 23 87  1  0
 23 88  1  0
 24 89  1  1
 25 90  1  0
 25 91  1  0
 26 92  1  0
 26 93  1  0
 28 94  1  0
 28 95  1  0
 28 96  1  0
 29 97  1  1
 30 98  1  0
 30 99  1  0
 31100  1  0
 31101  1  0
 33102  1  0
 34103  1  1
 35104  1  0
 35105  1  0
 37106  1  0
 37107  1  0
 37108  1  0
 38109  1  0
 38110  1  0
 38111  1  0
 39112  1  0
 39113  1  0
 40114  1  0
 40115  1  0
 42116  1  0
 42117  1  0
 42118  1  0
 43119  1  0
 43120  1  0
 44121  1  0
 44122  1  0
 46123  1  0
 46124  1  0
 46125  1  0
 48126  1  0
 48127  1  0
 48128  1  0
 49129  1  0
 49130  1  0
 49131  1  0
M  END


  Mrv1652309022204502D          

 49 53  0  0  1  0            999 V2000
    4.2868  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -16.0875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -15.2625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.1473  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -16.0875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.5762  -15.6750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -16.5000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.1473  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -17.3250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.5762  -18.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -16.5000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.2907  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -17.3250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   20.7197  -16.9125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -17.7375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   21.4341  -17.3250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -17.7375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4308  -16.9623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.9611  -17.8808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -18.5625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.7197  -19.3875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -18.9750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -18.5625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -17.7375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   18.9552  -18.4912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9956  -16.7871    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6083  -16.1163    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 19 18  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  1  0  0  0
 22 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 22 29  1  0  0  0  0
 29 30  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 36 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 34 41  1  0  0  0  0
 41 42  1  1  0  0  0
 41 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 32 45  1  0  0  0  0
 27 45  1  0  0  0  0
 45 46  1  6  0  0  0
 24 47  1  0  0  0  0
 19 47  1  0  0  0  0
 47 48  1  0  0  0  0
 47 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0147269

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@]3(C)[C@@H]2CC[C@]2(O)[C@@H]4CC(C)(C)CC[C@]4(C)CC[C@@]32C)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C46H82O3/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-39(47)49-38-26-27-43(7)35(41(38,4)5)24-28-44(8)36(43)25-29-46(48)37-34-40(2,3)30-31-42(37,6)32-33-45(44,46)9/h35-38,48H,10-34H2,1-9H3/t35-,36+,37+,38-,42+,43-,44+,45-,46-/m0/s1

> <INCHI_KEY>
FWTRWEOVLCELMX-DJABKKCQSA-N

> <FORMULA>
C46H82O3

> <MOLECULAR_WEIGHT>
683.159

> <EXACT_MASS>
682.6263965

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
131

> <JCHEM_AVERAGE_POLARIZABILITY>
90.0134718109796

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,4aR,6aR,6bS,8aR,12aR,12bS,14aR,14bR)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-docosahydropicen-3-yl hexadecanoate

> <ALOGPS_LOGP>
10.36

> <JCHEM_LOGP>
13.648428183

> <ALOGPS_LOGS>
-7.71

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
0.6954845331803094

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
206.09980000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.33e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4aR,6aR,6bS,8aR,12aR,12bS,14aR,14bR)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1H-picen-3-yl hexadecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       8.002 -27.720   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336 -28.490   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.669 -27.720   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.003 -28.490   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      13.337 -27.720   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.670 -28.490   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.004 -27.720   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.338 -28.490   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      18.672 -27.720   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.005 -28.490   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      21.339 -27.720   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      22.673 -28.490   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      24.006 -27.720   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      25.340 -28.490   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      26.674 -27.720   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      28.007 -28.490   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      28.007 -30.030   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      29.341 -27.720   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      30.675 -28.490   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      32.008 -27.720   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      33.342 -28.490   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      33.342 -30.030   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      34.676 -29.260   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      32.008 -30.800   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      32.008 -32.340   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      33.342 -33.110   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      34.676 -32.340   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      34.676 -33.880   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      34.676 -30.800   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      36.009 -30.030   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      37.343 -30.800   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      37.343 -32.340   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      38.677 -31.570   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      38.677 -33.110   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      40.010 -32.340   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      41.344 -33.110   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      41.871 -31.663   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      42.861 -33.377   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      41.344 -34.650   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      40.010 -35.420   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      38.677 -34.650   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      38.677 -36.190   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      37.343 -35.420   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      36.009 -34.650   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      36.009 -33.110   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      35.383 -34.517   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      30.675 -30.030   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      29.859 -31.336   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      29.136 -30.084   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   47                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   29                                             
CONECT   23   22                                                            
CONECT   24   22   25   47                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   45                                             
CONECT   28   27                                                            
CONECT   29   27   22   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   34   45                                             
CONECT   33   32                                                            
CONECT   34   32   35   41                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38   39                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   36   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   34   42   43                                             
CONECT   42   41                                                            
CONECT   43   41   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   32   27   46                                             
CONECT   46   45                                                            
CONECT   47   24   19   48   49                                             
CONECT   48   47                                                            
CONECT   49   47                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  106    0
END

View in JSmol

Synonyms

Value	Source
3b-(Palmitoyloxy)oleanan-13-ol	Generator
3Β-(palmitoyloxy)oleanan-13-ol	Generator

Chemical Formula

C₄₆H₈₂O₃

Average Mass

683.1590 Da

Monoisotopic Mass

682.62640 Da

IUPAC Name

(3S,4aR,6aR,6bS,8aR,12aR,12bS,14aR,14bR)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-docosahydropicen-3-yl hexadecanoate

Traditional Name

(3S,4aR,6aR,6bS,8aR,12aR,12bS,14aR,14bR)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1H-picen-3-yl hexadecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCC(=O)O[C@H]1CC[C@@]2(C)[C@@H](CC[C@]3(C)[C@@H]2CC[C@]2(O)[C@@H]4CC(C)(C)CC[C@]4(C)CC[C@@]32C)C1(C)C

InChI Identifier

InChI=1S/C46H82O3/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-23-39(47)49-38-26-27-43(7)35(41(38,4)5)24-28-44(8)36(43)25-29-46(48)37-34-40(2,3)30-31-42(37,6)32-33-45(44,46)9/h35-38,48H,10-34H2,1-9H3/t35-,36+,37+,38-,42+,43-,44+,45-,46-/m0/s1

InChI Key

FWTRWEOVLCELMX-DJABKKCQSA-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
Pentaclethra eetveldeana	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
Fatty acid ester
Fatty acyl
Tertiary alcohol
Cyclic alcohol
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	10.36	ALOGPS
logP	13.65	ChemAxon
logS	-7.7	ALOGPS
pKa (Strongest Basic)	0.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	206.1 m³·mol⁻¹	ChemAxon
Polarizability	90.01 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8684168

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10508767

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate (NP0147269)

MOL for NP0147269 ((3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate)

3D MOL for NP0147269 ((3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate)

3D SDF for NP0147269 ((3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate)

3D-SDF for NP0147269 ((3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate)

PDB for NP0147269 ((3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate)

3D PDB for NP0147269 ((3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate)

SMILES for NP0147269 ((3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate)

INCHI for NP0147269 ((3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate)

Structure for NP0147269 ((3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate)

3D Structure for NP0147269 ((3s,4ar,6ar,6bs,8ar,12ar,12bs,14ar,14br)-12b-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-tetradecahydro-1h-picen-3-yl hexadecanoate)