NP-MRD: Showing NP-Card for (1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate (NP0217075)

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Record Information

Version

2.0

Created at

2022-09-05 17:17:45 UTC

Updated at

2022-09-05 17:17:45 UTC

NP-MRD ID

NP0217075

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate

Description

(1R,2R,3R,4S,5R,6S,7S,8R,10R,14R)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-10-[(R)-methanesulfinyl]-6,10,14-trimethyl-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0²,⁷]Pentadecan-4-yl butanoate belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton. (1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate is found in Klyxum simplex. Based on a literature review very few articles have been published on (1R,2R,3R,4S,5R,6S,7S,8R,10R,14R)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-10-[(R)-methanesulfinyl]-6,10,14-trimethyl-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0²,⁷]Pentadecan-4-yl butanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052219172D          

 41 43  0  0  1  0            999 V2000
   -1.7518    8.8441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2367    8.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9011    7.4230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3861    6.7556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2065    6.8418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0505    6.0019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354    5.3345    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1999    4.5808    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3794    4.4946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0438    3.7409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8945    5.1620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6848    3.9134    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5053    3.9996    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2197    3.5871    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5553    2.8334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3838    2.0264    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2043    2.1127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7193    1.2728    0.0000 S   0  3  1  0  0  0  0  0  0  0  0  0
   -4.2344    0.6053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5398    1.1865    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -3.7707    1.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9502    1.3882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2357    1.8007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9002    2.5543    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2871    2.0023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1857    2.9668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4712    2.5543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4712    1.7293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2432    2.9668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9577    2.5543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6722    2.9668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0717    3.3613    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1175    3.7427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8408    4.7533    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5248    4.2919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4139    5.3467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3559    5.4207    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6915    6.1744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5119    6.2606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9969    5.5932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8475    7.0143    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  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  6  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  1  0  0  0
 18 19  1  0  0  0  0
 18 20  1  1  0  0  0
 16 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  1  0  0  0
 24 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 24 32  1  0  0  0  0
 12 32  1  0  0  0  0
 32 33  1  1  0  0  0
 14 33  1  1  0  0  0
 13 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  6  0  0  0
 34 37  1  0  0  0  0
  7 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
M  CHG  2  18   1  20  -1
M  END

     RDKit          3D

 93 95  0  0  0  0  0  0  0  0999 V2000
    6.4793   -1.0705   -0.4629 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2923   -2.4969   -0.0288 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.8845   -2.1757    0.3352 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3861   -0.9233    0.5604 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2007   -0.3987    0.0226 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1378   -0.0518    1.0166 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9984   -1.0472    2.1368 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6502   -2.4375    1.6595 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2282   -1.1470    2.9863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1365    0.0805    0.2485 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0109    1.4226   -0.5201 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8755    2.2630    0.3332 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5975    3.4172   -0.2967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9567    3.5044    0.4337 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -4.0367    1.2693    1.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8414   -0.1166    0.4840 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4994   -0.7636    0.8074 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7539   -1.5992    2.0424 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1872   -1.5810   -0.3171 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9671   -2.6332   -0.7535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0161   -2.8584   -0.0888 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6041   -3.4619   -1.9376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6455   -4.5370   -2.1740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3060   -5.3826   -3.3558 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3877    0.2307    1.0251 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9114    1.3283    0.3451 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3769    1.8729   -0.7482 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9053    2.9320    0.1758 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3833    2.4812   -2.0404 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4091    0.7583   -0.8969 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4630    0.2954   -2.2321 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5809    0.4822   -3.0210 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5878   -0.0263   -4.4250 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5824    1.0788   -2.5498 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5338   -0.7944   -0.3735 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1763   -0.9060   -1.5179 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8989   -0.4278    0.2505 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2076   -2.8454    0.4940 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1066   -3.1178   -0.9421 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0764   -3.6490    1.3717 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3737   -1.9235    1.7946 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7808   -1.2439   -0.6031 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3981    0.9195    1.5099 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5329   -3.0844    1.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2191   -2.4609    0.6603 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9378   -1.0214    4.0491 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9817   -0.3609    2.7879 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6743   -2.1800    2.9569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2094   -0.7630   -0.4649 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5754    2.3994    1.3618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8253    3.1682   -1.3358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1103    4.3804   -0.1517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3352    5.1626    0.7474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6625    5.5873    0.0806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8687    4.7935   -0.9784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6685    4.9460    3.6998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6239    4.6944    2.2023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1262    5.7587    2.1922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8892    2.8937   -0.0995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6800    2.0036   -1.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1129    1.2732    1.4105 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4926    1.4420    2.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9345   -0.0166   -0.6317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6525   -0.8131    0.7774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7938   -1.5251    2.4101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1167   -1.2023    2.8533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4759   -2.6603    1.8944 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4822   -2.8862   -2.8586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7854   -5.1606   -1.2611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6168   -4.0074   -2.3393 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6796   -4.7881   -4.0712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2427   -5.7345   -3.8556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7387   -6.2618   -3.0293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2838    0.5461    2.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2333    3.2451    0.9674 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8673    2.6183    0.6806 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2101    3.8834   -0.3532 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4929    2.9246   -2.1999 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3917    1.2439   -0.7001 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1787   -0.9490   -4.5162 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0611    0.7512   -5.0471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5354   -0.1565   -4.7887 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 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 39 41  2  0
 37 34  1  0
 34 35  1  0
 34 36  1  6
 34 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  1
 16 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 24 26  1  6
 26 27  1  0
 27 28  2  0
 27 29  1  0
 29 30  1  0
 30 31  1  0
 24 32  1  0
 32 33  1  0
 32 12  1  0
 12  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  1  0
 16 18  1  0
 18 19  1  0
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  8  7  1  0
 12 13  1  0
 33 14  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
 37 90  1  1
 40 91  1  0
 40 92  1  0
 40 93  1  0
 35 86  1  0
 35 87  1  0
 35 88  1  0
 36 89  1  0
 13 59  1  6
 14 60  1  1
 15 61  1  0
 15 62  1  0
 17 63  1  0
 17 64  1  0
 17 65  1  0
 21 69  1  0
 21 70  1  0
 22 71  1  0
 22 72  1  0
 23 73  1  0
 23 74  1  0
 25 75  1  0
 25 76  1  0
 25 77  1  0
 29 78  1  0
 29 79  1  0
 30 80  1  0
 30 81  1  0
 31 82  1  0
 31 83  1  0
 31 84  1  0
 32 85  1  1
 12 58  1  6
  8 50  1  1
  9 51  1  0
 10 52  1  0
 10 53  1  0
 10 54  1  0
 11 55  1  0
 11 56  1  0
 11 57  1  0
 19 66  1  0
 19 67  1  0
 19 68  1  0
M  CHG  2  18   1  20  -1
M  END


  Mrv1652309052219172D          

 41 43  0  0  1  0            999 V2000
   -1.7518    8.8441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2367    8.1767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9011    7.4230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3861    6.7556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2065    6.8418    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0505    6.0019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5354    5.3345    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1999    4.5808    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3794    4.4946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0438    3.7409    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8945    5.1620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6848    3.9134    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5053    3.9996    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2197    3.5871    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5553    2.8334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3838    2.0264    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2043    2.1127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7193    1.2728    0.0000 S   0  3  1  0  0  0  0  0  0  0  0  0
   -4.2344    0.6053    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5398    1.1865    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -3.7707    1.4744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9502    1.3882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2357    1.8007    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9002    2.5543    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2871    2.0023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1857    2.9668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4712    2.5543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4712    1.7293    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2432    2.9668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9577    2.5543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6722    2.9668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0717    3.3613    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1175    3.7427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8408    4.7533    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5248    4.2919    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4139    5.3467    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3559    5.4207    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.6915    6.1744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5119    6.2606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9969    5.5932    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8475    7.0143    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  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  6  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  1  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  1  0  0  0
 18 19  1  0  0  0  0
 18 20  1  1  0  0  0
 16 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  1  0  0  0
 24 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 24 32  1  0  0  0  0
 12 32  1  0  0  0  0
 32 33  1  1  0  0  0
 14 33  1  1  0  0  0
 13 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  6  0  0  0
 34 37  1  0  0  0  0
  7 37  1  0  0  0  0
 37 38  1  6  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
M  CHG  2  18   1  20  -1
M  END
> <DATABASE_ID>
NP0217075

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@@](C)(O)[C@@H]2[C@H]3C[C@@](C)(CCC[C@@](C)(OC(=O)CCC)[C@H](O3)[C@@H]2[C@H]1C(C)C)[S@@+](C)[O-]

> <INCHI_IDENTIFIER>
InChI=1S/C31H52O9S/c1-10-13-21(33)39-26-23(18(3)4)24-25(31(8,35)28(26)37-19(5)32)20-17-29(6,41(9)36)15-12-16-30(7,27(24)38-20)40-22(34)14-11-2/h18,20,23-28,35H,10-17H2,1-9H3/t20-,23-,24-,25-,26+,27-,28-,29-,30-,31+,41-/m1/s1

> <INCHI_KEY>
YAYZNOPNGRNCRX-SOULAQCXSA-N

> <FORMULA>
C31H52O9S

> <MOLECULAR_WEIGHT>
600.81

> <EXACT_MASS>
600.333204428

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
65.92973555136828

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,4S,5R,6S,7S,8R,10R,14R)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-10-[(R)-methanesulfinyl]-6,10,14-trimethyl-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-4-yl butanoate

> <JCHEM_LOGP>
3.0790800163333323

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.630076712060912

> <JCHEM_PKA_STRONGEST_BASIC>
-3.398004446144557

> <JCHEM_POLAR_SURFACE_AREA>
125.43000000000004

> <JCHEM_REFRACTIVITY>
155.28979999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,4S,5R,6S,7S,8R,10R,14R)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(R)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-4-yl butanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -3.270  16.509   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.175  15.263   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.549  13.856   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.454  12.610   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -5.986  12.771   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      -3.828  11.204   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -4.733   9.958   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.106   8.551   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.575   8.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.948   6.983   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.670   9.636   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.012   7.305   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.543   7.466   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -7.877   6.696   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.503   5.289   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -8.183   3.783   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -9.715   3.944   0.000  0.00  0.00           C+0
HETATM   18  S   UNK     0      -8.809   2.376   0.000  0.00  0.00           S+1
HETATM   19  C   UNK     0      -7.904   1.130   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0     -10.341   2.215   0.000  0.00  0.00           O-1
HETATM   21  C   UNK     0      -7.039   2.752   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.507   2.591   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.173   3.361   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.547   4.768   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.403   3.738   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.213   5.538   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -0.880   4.768   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -0.880   3.228   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       0.454   5.538   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.788   4.768   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.121   5.538   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.867   6.274   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -5.819   6.986   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -7.170   8.873   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -8.446   8.012   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -8.239   9.981   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      -6.264  10.119   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -6.891  11.526   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -8.422  11.686   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -9.327  10.441   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -9.049  13.093   0.000  0.00  0.00           O+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   37                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8   13   32                                                  
CONECT   13   12   14   34                                                  
CONECT   14   13   15   33                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18   21                                             
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   16   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   26   32                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30                                                            
CONECT   32   24   12   33                                                  
CONECT   33   32   14                                                       
CONECT   34   13   35   36   37                                             
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   34    7   38                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   86    0
END

View in JSmol

Synonyms

Value	Source
(1R,2R,3R,4S,5R,6S,7S,8R,10R,14R)-5-(Acetyloxy)-14-(butanoyloxy)-6-hydroxy-10-[(R)-methanesulfinyl]-6,10,14-trimethyl-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0,]pentadecan-4-yl butanoic acid	Generator
(1R,2R,3R,4S,5R,6S,7S,8R,10R,14R)-5-(Acetyloxy)-14-(butanoyloxy)-6-hydroxy-10-[(R)-methanesulphinyl]-6,10,14-trimethyl-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0,]pentadecan-4-yl butanoate	Generator
(1R,2R,3R,4S,5R,6S,7S,8R,10R,14R)-5-(Acetyloxy)-14-(butanoyloxy)-6-hydroxy-10-[(R)-methanesulphinyl]-6,10,14-trimethyl-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0,]pentadecan-4-yl butanoic acid	Generator

Chemical Formula

C₃₁H₅₂O₉S

Average Mass

600.8100 Da

Monoisotopic Mass

600.33320 Da

IUPAC Name

(1R,2R,3R,4S,5R,6S,7S,8R,10R,14R)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-10-[(R)-methanesulfinyl]-6,10,14-trimethyl-3-(propan-2-yl)-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-4-yl butanoate

Traditional Name

(1R,2R,3R,4S,5R,6S,7S,8R,10R,14R)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(R)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0^{2,7}]pentadecan-4-yl butanoate

CAS Registry Number

Not Available

SMILES

CCCC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@@](C)(O)[C@@H]2[C@H]3C[C@@](C)(CCC[C@@](C)(OC(=O)CCC)[C@H](O3)[C@@H]2[C@H]1C(C)C)[S@@+](C)[O-]

InChI Identifier

InChI=1S/C31H52O9S/c1-10-13-21(33)39-26-23(18(3)4)24-25(31(8,35)28(26)37-19(5)32)20-17-29(6,41(9)36)15-12-16-30(7,27(24)38-20)40-22(34)14-11-2/h18,20,23-28,35H,10-17H2,1-9H3/t20-,23-,24-,25-,26+,27-,28-,29-,30-,31+,41-/m1/s1

InChI Key

YAYZNOPNGRNCRX-SOULAQCXSA-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
Klyxum simplex	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Eunicellane and asbestinane diterpenoids

Alternative Parents

Substituents

Cladiellane diterpenoid
Eunicellane-type diterpenoid
Tricarboxylic acid or derivatives
Fatty acid ester
Cyclitol or derivatives
Fatty acyl
Cyclic alcohol
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Sulfoxide
Carboxylic acid derivative
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Sulfinyl compound
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
Organosulfur compound
Organic oxide
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	3.08	ChemAxon
pKa (Strongest Acidic)	13.63	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	125.43 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	155.29 m³·mol⁻¹	ChemAxon
Polarizability	65.93 Å³	ChemAxon
Number of Rings	3	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

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

162905481

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate (NP0217075)

MOL for NP0217075 ((1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate)

3D MOL for NP0217075 ((1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate)

3D SDF for NP0217075 ((1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate)

3D-SDF for NP0217075 ((1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate)

PDB for NP0217075 ((1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate)

3D PDB for NP0217075 ((1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate)

SMILES for NP0217075 ((1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate)

INCHI for NP0217075 ((1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate)

Structure for NP0217075 ((1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate)

3D Structure for NP0217075 ((1r,2r,3r,4s,5r,6s,7s,8r,10r,14r)-5-(acetyloxy)-14-(butanoyloxy)-6-hydroxy-3-isopropyl-10-[(r)-methanesulfinyl]-6,10,14-trimethyl-15-oxatricyclo[6.6.1.0²,⁷]pentadecan-4-yl butanoate)