NP-MRD: Showing NP-Card for (-)-Rouremin (NP0074158)

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Record Information

Version

2.0

Created at

2022-04-28 19:19:22 UTC

Updated at

2022-04-28 19:19:22 UTC

NP-MRD ID

NP0074158

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Rouremin

Description

(2R)-1-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(hexadecanoyloxy)propan-2-yl icosanoate belongs to the class of organic compounds known as glycosyldiacylglycerols. These are diacylglycerols that carry a saccharide moiety linked to the glycerol. (-)-Rouremin is found in Rourea minor . Based on a literature review very few articles have been published on (2R)-1-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(hexadecanoyloxy)propan-2-yl icosanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282221192D          

 55 55  0  0  1  0            999 V2000
    9.2881   -9.4875    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.2881   -8.6625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.0026   -8.2500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7171   -8.6625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.7171   -9.4875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -9.9000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0026  -10.7250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171  -11.9625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.0026  -12.3750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460  -11.9625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605  -13.2000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775  -11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -8.6625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -8.2500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -9.9000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  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
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
  9 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 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
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
  4 51  1  1  0  0  0
 51 52  1  0  0  0  0
  3 53  1  6  0  0  0
  2 54  1  1  0  0  0
  1 55  1  6  0  0  0
M  END

     RDKit          3D

142142  0  0  0  0  0  0  0  0999 V2000
    0.9849    7.0904    4.5694 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1714    6.3741    5.8918 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875    5.7577    5.9059 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6986    4.7934    4.7486 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0463    4.1420    4.6864 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3300    3.3784    5.9435 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7010    2.7025    5.8116 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6715    1.7722    4.6293 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5742    0.6851    4.7691 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9680   -0.2075    5.8776 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0713   -1.2541    6.3867 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4755   -2.2885    5.5069 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4470   -1.7410    4.5894 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8004   -2.7594    3.6687 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7406   -3.4445    2.7392 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4907   -2.4475    1.8674 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3942   -3.1143    0.8663 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5997   -3.9711   -0.1171 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6457   -3.0343   -0.7910 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7885   -3.6213   -1.8305 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5558   -3.5100   -1.8323 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3175   -4.3493   -2.9006 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5474   -4.9120   -3.9472 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8679   -4.1170   -5.2451 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5017   -2.7653   -5.0650 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1853   -2.4026   -4.9373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6941   -3.3029   -5.0187 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2502   -0.9770   -4.7007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7326   -0.9139   -4.8285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3375    0.4351   -4.5771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8067    1.5119   -5.4832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4463    2.8491   -5.2312 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2242    3.2832   -3.8001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8565    4.6562   -3.5746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6479    5.1008   -2.1630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2783    4.1581   -1.1622 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0548    4.6162    0.2558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6344    5.9129    0.6315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0970    6.0929    0.5881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9753    5.3406    1.4888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0617    3.8713    1.4605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5038    3.2563    0.1617 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6407   -6.3611   -4.1586 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1781   -7.0942   -3.0949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1691   -6.9495   -2.8693 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5166   -6.4012   -1.6389 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8851   -6.4970   -1.4324 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4445   -5.5185   -0.4472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8459   -5.7146    0.8639 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3856   -7.8818   -1.1777 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7473   -7.8828   -1.5279 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5993   -8.8530   -2.0005 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7072   -9.6112   -1.2367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9724   -8.1998   -3.1645 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9187   -8.0090   -4.1777 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.9807    7.4737    4.2607 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2447    7.8798    4.6855 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4990    5.5205    6.0181 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0163    7.0751    6.7276 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3314    6.5594    5.7692 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6510    5.2417    6.8724 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4648    5.3159    3.7763 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8854    4.0354    4.8378 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8283    4.9491    4.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1498    3.5161    3.7628 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5608    2.6229    6.1795 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4241    4.0908    6.8092 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4122    3.5384    5.5552 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0064    2.2580    6.7461 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6145    2.2663    3.6833 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6752    1.2353    4.6754 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6456    0.0914    3.8052 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5924    1.1547    4.8306 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3945    0.4144    6.7339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8850   -0.7808    5.4725 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2483   -0.6976    6.9585 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6207   -1.7422    7.2667 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2858   -2.8391    4.9520 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9581   -3.0227    6.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7505   -0.8520    4.0685 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5743   -1.4379    5.2795 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3380   -3.5167    4.3194 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9745   -2.2173    3.1266 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4116   -4.0754    3.3124 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1613   -4.0724    2.0395 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1935   -1.9357    2.5994 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8607   -1.6535    1.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1704   -3.6919    1.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8949   -2.3295    0.2739 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3573   -4.3551   -0.8523 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1445   -4.8545    0.3560 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9386   -2.6770    0.0231 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2477   -2.1790   -1.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5075   -4.6374   -3.6924 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9641   -4.1282   -5.3983 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3643   -4.5374   -6.1101 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1114   -0.6690   -3.6960 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2562   -0.3616   -5.4549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1999   -1.6786   -4.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0183   -1.2105   -5.8786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2657    0.7325   -3.5087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4357    0.3451   -4.7930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7106    1.6708   -5.3430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0259    1.2418   -6.5355 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5174    2.9125   -5.5153 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.1628    3.3762   -3.5893 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652304282221192D          

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  9 32  1  0  0  0  0
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 34 35  2  0  0  0  0
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  3 53  1  6  0  0  0
  2 54  1  1  0  0  0
  1 55  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0074158

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCCC(=O)O[C@H](CO[C@@H]1O[C@H](CN)[C@@H](O)[C@H](O)[C@H]1O)COC(=O)CCCCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C45H87NO9/c1-3-5-7-9-11-13-15-17-18-19-20-22-24-26-28-30-32-34-41(48)54-38(37-53-45-44(51)43(50)42(49)39(35-46)55-45)36-52-40(47)33-31-29-27-25-23-21-16-14-12-10-8-6-4-2/h38-39,42-45,49-51H,3-37,46H2,1-2H3/t38-,39+,42+,43-,44+,45+/m0/s1

> <INCHI_KEY>
ADDGQEWZHSZZRP-YHMQSLHSSA-N

> <FORMULA>
C45H87NO9

> <MOLECULAR_WEIGHT>
786.189

> <EXACT_MASS>
785.638083385

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
142

> <JCHEM_AVERAGE_POLARIZABILITY>
100.50378022908293

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-1-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(hexadecanoyloxy)propan-2-yl icosanoate

> <ALOGPS_LOGP>
8.41

> <JCHEM_LOGP>
11.903650999666667

> <ALOGPS_LOGS>
-6.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.239127759304953

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.217927287668118

> <JCHEM_PKA_STRONGEST_BASIC>
8.7961535819243

> <JCHEM_POLAR_SURFACE_AREA>
157.76999999999998

> <JCHEM_REFRACTIVITY>
220.17370000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
41

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.50e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-1-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(hexadecanoyloxy)propan-2-yl icosanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      17.338 -17.710   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.338 -16.170   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      18.672 -15.400   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.005 -16.170   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      20.005 -17.710   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      18.672 -18.480   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      18.672 -20.020   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      20.005 -20.790   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.005 -22.330   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      18.672 -23.100   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      17.338 -22.330   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      17.338 -20.790   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      16.004 -23.100   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      14.670 -22.330   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.337 -23.100   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.003 -22.330   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.669 -23.100   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336 -22.330   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002 -23.100   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.668 -22.330   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.335 -23.100   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001 -22.330   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667 -23.100   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334 -22.330   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000 -23.100   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.334 -22.330   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.667 -23.100   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.001 -22.330   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -5.335 -23.100   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -6.668 -22.330   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -8.002 -23.100   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      21.339 -23.100   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      22.673 -22.330   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      24.006 -23.100   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      24.006 -24.640   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      25.340 -22.330   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      26.674 -23.100   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      28.007 -22.330   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      29.341 -23.100   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      30.675 -22.330   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      32.008 -23.100   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      33.342 -22.330   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      34.676 -23.100   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      36.009 -22.330   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      37.343 -23.100   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      38.677 -22.330   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      40.010 -23.100   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      41.344 -22.330   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      42.678 -23.100   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      44.011 -22.330   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      21.339 -15.400   0.000  0.00  0.00           C+0
HETATM   52  N   UNK     0      22.673 -16.170   0.000  0.00  0.00           N+0
HETATM   53  O   UNK     0      18.672 -13.860   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0      16.004 -15.400   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0      16.004 -18.480   0.000  0.00  0.00           O+0
CONECT    1    2    6   55                                                  
CONECT    2    1    3   54                                                  
CONECT    3    2    4   53                                                  
CONECT    4    3    5   51                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   32                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32    9   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49                                                            
CONECT   51    4   52                                                       
CONECT   52   51                                                            
CONECT   53    3                                                            
CONECT   54    2                                                            
CONECT   55    1                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  110    0
END

View in JSmol

Synonyms

Value	Source
(2R)-1-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(hexadecanoyloxy)propan-2-yl icosanoic acid	Generator

Chemical Formula

C₄₅H₈₇NO₉

Average Mass

786.1890 Da

Monoisotopic Mass

785.63808 Da

IUPAC Name

(2R)-1-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(hexadecanoyloxy)propan-2-yl icosanoate

Traditional Name

(2R)-1-{[(2R,3R,4S,5S,6R)-6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(hexadecanoyloxy)propan-2-yl icosanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCCC(=O)O[C@H](CO[C@@H]1O[C@H](CN)[C@@H](O)[C@H](O)[C@H]1O)COC(=O)CCCCCCCCCCCCCCC

InChI Identifier

InChI=1S/C45H87NO9/c1-3-5-7-9-11-13-15-17-18-19-20-22-24-26-28-30-32-34-41(48)54-38(37-53-45-44(51)43(50)42(49)39(35-46)55-45)36-52-40(47)33-31-29-27-25-23-21-16-14-12-10-8-6-4-2/h38-39,42-45,49-51H,3-37,46H2,1-2H3/t38-,39+,42+,43-,44+,45+/m0/s1

InChI Key

ADDGQEWZHSZZRP-YHMQSLHSSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Rourea minor	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glycosyldiacylglycerols. These are diacylglycerols that carry a saccharide moiety linked to the glycerol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Glycosylglycerols

Direct Parent

Glycosyldiacylglycerols

Alternative Parents

Substituents

Glycosyldiacylglycerol
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Glycosyl compound
O-glycosyl compound
Fatty acid ester
Amino saccharide
Dicarboxylic acid or derivatives
Fatty acyl
Monosaccharide
Oxane
Amino acid or derivatives
Carboxylic acid ester
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Polyol
Amine
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Alcohol
Carbonyl group
Primary aliphatic amine
Primary amine
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	8.41	ALOGPS
logP	11.9	ChemAxon
logS	-6.7	ALOGPS
pKa (Strongest Acidic)	12.22	ChemAxon
pKa (Strongest Basic)	8.8	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	157.77 Å²	ChemAxon
Rotatable Bond Count	41	ChemAxon
Refractivity	220.17 m³·mol⁻¹	ChemAxon
Polarizability	100.5 Å³	ChemAxon
Number of Rings	1	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163031704

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Rouremin (NP0074158)

MOL for NP0074158 ((-)-Rouremin)

3D MOL for NP0074158 ((-)-Rouremin)

3D SDF for NP0074158 ((-)-Rouremin)

3D-SDF for NP0074158 ((-)-Rouremin)

PDB for NP0074158 ((-)-Rouremin)

3D PDB for NP0074158 ((-)-Rouremin)

SMILES for NP0074158 ((-)-Rouremin)

INCHI for NP0074158 ((-)-Rouremin)

Structure for NP0074158 ((-)-Rouremin)

3D Structure for NP0074158 ((-)-Rouremin)