NP-MRD: Showing NP-Card for (1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate (NP0166075)

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Record Information

Version

2.0

Created at

2022-09-03 01:22:52 UTC

Updated at

2022-09-03 01:22:52 UTC

NP-MRD ID

NP0166075

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate

Description

Milolide N belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. (1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate is found in Briareum stechei. Based on a literature review very few articles have been published on Milolide N.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032203222D          

 41 43  0  0  1  0            999 V2000
    1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8083   -3.0590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0632   -3.8436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8702   -4.0152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5414   -4.5694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8218   -3.6263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7519   -2.9737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4584   -4.9320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2788   -5.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6913   -5.7327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6144   -4.2645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4214   -4.0930    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  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 25 23  1  6  0  0  0
 14 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 26 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
  7 35  1  0  0  0  0
 35 36  1  0  0  0  0
 33 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 31 40  1  0  0  0  0
 40 41  1  1  0  0  0
M  END

     RDKit          3D

 83 85  0  0  0  0  0  0  0  0999 V2000
    7.2808    2.7019    0.2256 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9659    2.1293   -0.2101 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2600    1.4131    0.9364 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9670    0.8658    0.4544 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6442    1.0368   -0.7251 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1664    0.1969    1.2899 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8662   -0.3972    0.9668 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7966    0.3264    1.6738 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1910    1.0475    0.7373 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1117    0.7295   -0.6012 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6342    1.5349   -1.5701 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8965    1.0585   -2.9727 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9221    2.7245   -1.3293 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6394    0.7885    1.0098 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9702    0.5335    2.4730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2878    2.2086    0.8796 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4182    3.1788    0.4366 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1463    4.2799    1.2258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2271    5.3749    0.8470 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7036    4.4079    2.3752 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5495    2.1976    0.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3502    1.0976    0.6489 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7754   -0.1159    0.6681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4155   -1.3069    1.2315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3648   -0.0879    0.0533 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0857   -1.3885   -0.4518 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3815   -1.3536   -1.8929 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4571   -1.9116   -2.4906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6239   -1.8089   -3.9651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2997   -2.5028   -1.8350 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8504   -2.1877   -0.4092 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0418   -2.0335   -1.4558 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2365   -2.4440    0.9191 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1740   -2.7352    1.0203 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0892   -1.8158    1.0412 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5201   -2.3593    1.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8927   -3.6421    1.4707 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8923   -4.0102    0.6382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0300   -4.5079    0.8649 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2957   -3.6692   -0.6969 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1242   -4.5304   -1.0138 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2050    3.8212    0.2541 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5455    2.3629    1.2614 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1279    2.4060   -0.4302 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1713    1.4238   -1.0616 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3266    2.9439   -0.6183 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9539    0.5602    1.2072 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1662    2.1185    1.7643 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8053   -0.0343   -0.1200 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3588   -0.0721    2.5756 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3622    1.2275    2.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0732    2.1545    0.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1915   -0.0019   -3.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0359    1.3025   -3.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7597    1.6209   -3.4129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9646    1.0010    2.6971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0679   -0.4987    2.7695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2200    1.0424    3.0762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6327    2.5433    1.9157 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3720    5.1141   -0.0397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7962    6.3074    0.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4432    5.6471    1.7057 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4200    2.1629   -1.0309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0751    3.1638    0.3436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3293    1.1988    1.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6853   -2.0058    1.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0601   -1.0307    2.1457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1642   -1.8129    0.5980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4564    0.6034   -0.8844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9303   -2.0839   -0.1032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7148   -1.8596   -4.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0493   -2.5876   -4.4977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3011   -0.7654   -4.2412 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9675   -1.9287   -1.2649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6446   -1.7457    1.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4755   -3.8283    1.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6351   -2.9899    2.0422 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2388   -1.5074    1.1040 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7575   -2.9932    0.2792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0681   -3.7521   -1.4191 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7631   -3.9098   -1.1859 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0547   -5.2910   -0.2164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3385   -5.0507   -1.9948 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  2  0
  4  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
 11 13  2  0
  9 14  1  0
 14 15  1  1
 14 16  1  0
 16 21  1  0
 21 22  1  0
 22 23  2  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  2  0
 26 31  1  0
 31 32  1  6
 31 40  1  0
 40 41  1  0
 40 38  1  0
 38 39  2  0
 38 37  1  0
 37 33  1  0
 33 34  1  0
 34 35  2  0
 35 36  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  2  0
 35  7  1  0
 25 14  1  0
 33 31  1  0
  1 42  1  0
  1 43  1  0
  1 44  1  0
  2 45  1  0
  2 46  1  0
  3 47  1  0
  3 48  1  0
  7 49  1  6
  8 50  1  0
  8 51  1  0
  9 52  1  6
 12 53  1  0
 12 54  1  0
 12 55  1  0
 15 56  1  0
 15 57  1  0
 15 58  1  0
 16 59  1  1
 21 63  1  0
 21 64  1  0
 22 65  1  0
 24 66  1  0
 24 67  1  0
 24 68  1  0
 25 69  1  6
 26 70  1  1
 29 71  1  0
 29 72  1  0
 29 73  1  0
 32 74  1  0
 40 80  1  6
 41 81  1  0
 41 82  1  0
 41 83  1  0
 33 75  1  1
 34 76  1  0
 36 77  1  0
 36 78  1  0
 36 79  1  0
 19 60  1  0
 19 61  1  0
 19 62  1  0
M  END


  Mrv1652309032203222D          

 41 43  0  0  1  0            999 V2000
    1.4289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.7158   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8083   -3.0590    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0632   -3.8436    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8702   -4.0152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5414   -4.5694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.8218   -3.6263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7519   -2.9737    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4584   -4.9320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2788   -5.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6913   -5.7327    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6144   -4.2645    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.4214   -4.0930    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  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 25 23  1  6  0  0  0
 14 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  6  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 26 31  1  0  0  0  0
 31 32  1  1  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
  7 35  1  0  0  0  0
 35 36  1  0  0  0  0
 33 37  1  1  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 31 40  1  0  0  0  0
 40 41  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0166075

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C30H42O11/c1-9-10-25(34)40-21-14-23(38-19(6)32)29(8)22(37-18(5)31)12-11-15(2)26(29)27(39-20(7)33)30(36)17(4)28(35)41-24(30)13-16(21)3/h11,13,17,21-24,26-27,36H,9-10,12,14H2,1-8H3/b16-13-/t17-,21+,22-,23+,24-,26+,27+,29+,30-/m0/s1

> <INCHI_KEY>
YABKAVBLXPBVRQ-DZXSCAIYSA-N

> <FORMULA>
C30H42O11

> <MOLECULAR_WEIGHT>
578.655

> <EXACT_MASS>
578.272712172

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
59.0991905661021

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3S,4R,7S,8Z,10R,12R,13R,14S)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadeca-8,16-dien-10-yl butanoate

> <ALOGPS_LOGP>
2.96

> <JCHEM_LOGP>
2.195999176666666

> <ALOGPS_LOGS>
-4.53

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.349866482979827

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9579684003446234

> <JCHEM_POLAR_SURFACE_AREA>
151.73000000000002

> <JCHEM_REFRACTIVITY>
144.03350000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.70e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3S,4R,7S,8Z,10R,12R,13R,14S)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadeca-8,16-dien-10-yl butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       2.667  -1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.335  -6.160   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       6.668  -3.850   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       8.002   1.540   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.669  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      12.003  -0.770   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      13.337  -0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      13.337   1.540   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      14.670  -0.770   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      13.337  -3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      10.842  -5.710   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      11.318  -7.175   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      12.824  -7.495   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      10.344  -8.530   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      10.867  -6.769   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.137  -5.551   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       8.322  -9.206   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       9.854  -9.367   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      10.624 -10.701   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      10.480  -7.960   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      11.987  -7.640   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   35                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9   15   16   25                                             
CONECT   15   14                                                            
CONECT   16   14   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   14   26                                                  
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28                                                            
CONECT   31   26   32   33   40                                             
CONECT   32   31                                                            
CONECT   33   31   34   37                                                  
CONECT   34   33   35                                                       
CONECT   35   34    7   36                                                  
CONECT   36   35                                                            
CONECT   37   33   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   31   41                                                  
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₂O₁₁

Average Mass

578.6550 Da

Monoisotopic Mass

578.27271 Da

IUPAC Name

(1S,2R,3S,4R,7S,8Z,10R,12R,13R,14S)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadeca-8,16-dien-10-yl butanoate

Traditional Name

(1S,2R,3S,4R,7S,8Z,10R,12R,13R,14S)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadeca-8,16-dien-10-yl butanoate

CAS Registry Number

Not Available

SMILES

CCCC(=O)O[C@@H]1C[C@@H](OC(C)=O)[C@@]2(C)[C@H](CC=C(C)[C@@H]2[C@@H](OC(C)=O)[C@]2(O)[C@@H](C)C(=O)O[C@H]2\C=C1\C)OC(C)=O

InChI Identifier

InChI=1S/C30H42O11/c1-9-10-25(34)40-21-14-23(38-19(6)32)29(8)22(37-18(5)31)12-11-15(2)26(29)27(39-20(7)33)30(36)17(4)28(35)41-24(30)13-16(21)3/h11,13,17,21-24,26-27,36H,9-10,12,14H2,1-8H3/b16-13-/t17-,21+,22-,23+,24-,26+,27+,29+,30-/m0/s1

InChI Key

YABKAVBLXPBVRQ-DZXSCAIYSA-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
Briareum stechei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Briarane diterpenoid
Pentacarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Gamma butyrolactone
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	2.96	ALOGPS
logP	2.2	ChemAxon
logS	-4.5	ALOGPS
pKa (Strongest Acidic)	12.35	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	151.73 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	144.03 m³·mol⁻¹	ChemAxon
Polarizability	59.1 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	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

C00045351

Chemspider ID

29213061

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11135613

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate (NP0166075)

MOL for NP0166075 ((1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate)

3D MOL for NP0166075 ((1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate)

3D SDF for NP0166075 ((1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate)

3D-SDF for NP0166075 ((1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate)

PDB for NP0166075 ((1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate)

3D PDB for NP0166075 ((1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate)

SMILES for NP0166075 ((1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate)

INCHI for NP0166075 ((1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate)

Structure for NP0166075 ((1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate)

3D Structure for NP0166075 ((1s,2r,3s,4r,7s,8z,10r,12r,13r,14s)-2,12,14-tris(acetyloxy)-3-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,16-dien-10-yl butanoate)