NP-MRD: Showing NP-Card for 7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate (NP0280381)

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Record Information

Version

2.0

Created at

2022-09-09 06:08:14 UTC

Updated at

2022-09-09 06:08:15 UTC

NP-MRD ID

NP0280381

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate

Description

7-(Acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1H,2H,3H,3aH,4H,5H,6H,7H,8H,9H,12H,13H,13aH-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate belongs to the class of organic compounds known as jatrophane and cyclojatrophane diterpenoids. These are diterpenoids with a structure based on the jatrophane or the 9,13-jatrophane skeleton. Jatrophane can be derived from casbane by 6,10-cyclization and opening of the cyclopropane. Cyclojatrophane diterpenoids are based on the 9,13-cyclization of the jatrophane skeleton yields the 9,13-cyclojatrophane skeleton. 7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate is found in Euphorbia amygdaloides. 7-(Acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1H,2H,3H,3aH,4H,5H,6H,7H,8H,9H,12H,13H,13aH-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate is a strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171514592D          

 53 55  0  0  0  0            999 V2000
    5.7415   -4.6412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1895   -4.0281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825   -4.1996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1276   -4.9842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8305   -3.5865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0854   -2.8019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0235   -3.7581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4715   -3.1450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6645   -3.3165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4095   -4.1011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9616   -4.7142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7685   -4.5427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7066   -5.4988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1124   -2.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8575   -3.4880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0505   -3.6595    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4832   -2.6969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2044   -4.4442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3476   -5.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0927   -5.8419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143   -6.0134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2663   -5.4003    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0114   -4.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3055   -2.8749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3265   -3.4052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4950   -3.0745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2466   -2.2618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0084   -1.4772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8154   -1.3057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0869   -0.9184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5063   -0.5407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0703   -0.5211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5183    0.0920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8773   -0.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3923    0.3179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2898    0.3649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0967    0.1934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7098    0.7455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1830   -0.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6119   -0.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6119    0.1979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3264   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3264   -1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0409   -0.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0409    0.1979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7553   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4698   -0.6271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4293   -0.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1744   -1.7472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3674   -1.9188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7264   -2.3603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5334   -2.1888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 27 24  1  4  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  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
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
 39 49  1  0  0  0  0
 34 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
  8 52  1  0  0  0  0
 52 53  2  0  0  0  0
M  END

     RDKit          3D

102104  0  0  0  0  0  0  0  0999 V2000
   -1.3262    0.4129    1.9677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5503    0.2496    0.8566 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7197   -0.3974    1.1246 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6481   -1.4525    2.0600 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0427   -0.8617    0.3633 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.6296    0.4169    0.2379 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4094    0.8878    1.2926 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5461    0.1519    2.2875 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0521    2.1947    1.2488 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9201    2.9976    0.2139 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8774    2.6112    2.4033 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.4775    3.9913    2.1919 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1924    2.5619    3.6073 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7596    1.7185    4.4440 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6086   -1.7191   -0.7966 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0176   -2.1270   -0.5514 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6198   -2.8863   -0.7800 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3026   -2.2332   -0.4902 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7202   -2.9853    0.5229 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5490   -2.2506   -1.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9101   -1.3987   -2.5718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5565   -3.1199   -2.1802 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1162   -4.0088   -1.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1273   -4.0739   -3.0311 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5170   -2.3985   -3.0374 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6551   -1.8298   -2.8792 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6060   -1.5840   -1.8047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1873   -2.8368   -1.1824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9056   -0.9509   -2.4306 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.9462   -1.0347    1.4532 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.4819   -2.5028    3.7142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2346   -3.2355    4.8520 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0109   -3.8743    4.9842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1297   -3.7460    3.9963 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3343   -3.0402    2.8708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3941    0.4811   -0.8951 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3753    0.7797   -2.3407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9476    1.8563   -2.9134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8160    2.0044   -4.4044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5514    2.6807   -2.2213 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0393    0.7679   -0.4382 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9708    2.2146   -0.2476 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957    3.0395   -0.8742 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7153    2.5234   -1.6766 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1504    4.4699   -0.5758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1831    4.9461    0.3938 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6500    5.3467   -1.1142 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.3850    3.9585    0.1671 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3237    2.6699   -0.6109 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7433    1.8939    2.4746 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1028    4.1972    3.0641 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7304    4.7655    2.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.7491    1.7330    4.3223 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4419   -1.1072   -1.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6090   -2.2645   -1.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0282   -3.0271    0.0974 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5113   -1.2772    0.0066 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6533   -3.3770   -1.7813 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9132   -3.6075    0.0074 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3279   -3.5758    0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3558   -4.8309   -0.9130 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9398   -4.6017   -1.6046 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3931   -3.4973   -0.2088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4965   -4.2925   -3.7472 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.4633   -2.0050    3.6321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9742   -3.3204    5.6392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7748   -4.4586    5.8594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5924   -2.9842    2.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0045    1.3890   -0.5525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1860    2.8997   -4.6371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3941    1.0925   -4.8569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7936    2.1681   -4.8665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2389    0.6433   -1.1992 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4420    4.1000    1.0632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8462    5.8477    0.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1005    5.2146   -0.1947 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4238    5.0400   -1.8332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5012    7.1101   -0.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2220    7.3928   -1.4281 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7987    6.9053    0.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
 53 52  1  0
 52 50  2  0
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 46 41  1  0
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 31 28  1  0
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 28 30  1  0
 28 27  1  0
 27 26  2  0
 26 23  1  0
 23 24  1  0
 23 25  1  6
 23 21  1  0
 21 22  2  0
 21 19  1  0
 19 20  1  1
 19 18  1  0
 18 16  1  0
 16 17  1  0
 16  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
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 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
  6  5  1  0
  5  3  1  0
  3  4  1  0
  3  2  1  0
  2  1  2  3
  2 46  1  0
 40 35  1  0
  5 19  1  0
 53100  1  0
 53101  1  0
 53102  1  0
 52 99  1  0
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 41 91  1  1
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 31 86  1  1
 36 87  1  0
 37 88  1  0
 38 89  1  0
 40 90  1  0
 29 80  1  0
 29 81  1  0
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 30 83  1  0
 30 84  1  0
 30 85  1  0
 27 79  1  0
 26 78  1  0
 24 74  1  0
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 25 77  1  0
 20 73  1  0
 18 71  1  0
 18 72  1  0
 16 67  1  6
 17 68  1  0
 17 69  1  0
 17 70  1  0
  6 59  1  1
 11 60  1  0
 11 61  1  0
 12 62  1  1
 13 63  1  0
 13 64  1  0
 13 65  1  0
 15 66  1  0
  5 58  1  6
  3 56  1  1
  4 57  1  0
  1 54  1  0
  1 55  1  0
M  END


  Mrv1533004171514592D          

 53 55  0  0  0  0            999 V2000
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    5.1895   -4.0281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3825   -4.1996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1276   -4.9842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8305   -3.5865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0854   -2.8019    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0235   -3.7581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4715   -3.1450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6645   -3.3165    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4095   -4.1011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9616   -4.7142    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7685   -4.5427    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7066   -5.4988    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1124   -2.7034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8575   -3.4880    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4832   -2.6969    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3476   -5.0573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0927   -5.8419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7143   -6.0134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2663   -5.4003    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0114   -4.6157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3055   -2.8749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3265   -3.4052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4950   -3.0745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2466   -2.2618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0084   -1.4772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8154   -1.3057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0869   -0.9184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5063   -0.5407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0703   -0.5211    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5183    0.0920    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8773   -0.3495    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3923    0.3179    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2898    0.3649    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0967    0.1934    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7098    0.7455    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1830   -0.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8974   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6119   -0.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6119    0.1979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3264   -1.0396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3264   -1.8646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0409   -0.6271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0409    0.1979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7553   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4698   -0.6271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4293   -0.9626    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1744   -1.7472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3674   -1.9188    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7264   -2.3603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5334   -2.1888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
 14 24  1  0  0  0  0
 24 25  1  0  0  0  0
 24 26  1  0  0  0  0
 27 24  1  4  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 32 33  2  0  0  0  0
 32 34  1  0  0  0  0
 34 35  1  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
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  2  0  0  0  0
 41 43  1  0  0  0  0
 43 44  2  0  0  0  0
 43 45  1  0  0  0  0
 45 46  1  0  0  0  0
 45 47  1  0  0  0  0
 47 48  1  0  0  0  0
 39 49  1  0  0  0  0
 34 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 50 52  1  0  0  0  0
  8 52  1  0  0  0  0
 52 53  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0280381

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=C(C)C(=O)OC1C(OC(C)=O)C(OC(=O)C2=CC=CN=C2)C(C)(C)C=CC(C)(O)C(=O)C2(O)CC(C)C(OC(=O)C(=C)C(C)OO)C2C(O)C1=C

> <INCHI_IDENTIFIER>
InChI=1S/C38H49NO14/c1-11-19(2)32(42)51-29-22(5)27(41)26-28(50-33(43)21(4)23(6)53-48)20(3)17-38(26,47)35(45)37(10,46)15-14-36(8,9)31(30(29)49-24(7)40)52-34(44)25-13-12-16-39-18-25/h11-16,18,20,23,26-31,41,46-48H,4-5,17H2,1-3,6-10H3

> <INCHI_KEY>
UYWMRBXGOAEPNN-UHFFFAOYSA-N

> <FORMULA>
C38H49NO14

> <MOLECULAR_WEIGHT>
743.803

> <EXACT_MASS>
743.315305262

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
102

> <JCHEM_AVERAGE_POLARIZABILITY>
74.64546475619827

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1H,2H,3H,3aH,4H,5H,6H,7H,8H,9H,12H,13H,13aH-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate

> <ALOGPS_LOGP>
2.44

> <JCHEM_LOGP>
4.191700650333333

> <ALOGPS_LOGS>
-4.63

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.433548254803952

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.623390680899929

> <JCHEM_PKA_STRONGEST_BASIC>
3.2397726629878707

> <JCHEM_POLAR_SURFACE_AREA>
225.30999999999995

> <JCHEM_REFRACTIVITY>
187.39810000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.76e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1H,2H,3H,3aH,4H,6H,7H,8H-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0      10.717  -8.664   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.687  -7.519   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.181  -7.839   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.705  -9.304   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.150  -6.695   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.626  -5.230   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       5.644  -7.015   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.613  -5.871   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.107  -6.191   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       2.631  -7.655   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.662  -8.800   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.168  -8.480   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.186 -10.264   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.077  -5.046   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.601  -6.511   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.094  -6.831   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -0.902  -5.034   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -0.382  -8.296   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.649  -9.440   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.173 -10.905   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.333 -11.225   0.000  0.00  0.00           C+0
HETATM   22  N   UNK     0      -2.364 -10.081   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0      -1.888  -8.616   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.570  -5.367   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.609  -6.356   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.924  -5.739   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -0.460  -4.222   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.016  -2.757   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.522  -2.437   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.162  -1.714   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       0.945  -1.009   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       1.998  -0.973   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       0.967   0.172   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       3.504  -0.652   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       2.599   0.593   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       4.274   0.681   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       5.781   0.361   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       6.925   1.392   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.942  -1.171   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       7.275  -1.941   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       8.609  -1.171   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       8.609   0.369   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       9.943  -1.941   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       9.943  -3.481   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      11.276  -1.171   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      11.276   0.369   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      12.610  -1.941   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0      13.944  -1.171   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0       4.535  -1.797   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       4.059  -3.262   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       2.552  -3.582   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0       5.089  -4.406   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       6.596  -4.086   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   52                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    9   15   24                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
CONECT   24   14   25   26   27                                             
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   24   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31   32                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   29   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   35   36   49                                             
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   49                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   48                                                       
CONECT   48   47                                                            
CONECT   49   39   34   50                                                  
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50    8   53                                                  
CONECT   53   52                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  110    0
END

View in JSmol

Synonyms

Value	Source
7-(Acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1H,2H,3H,3ah,4H,5H,6H,7H,8H,9H,12H,13H,13ah-cyclopenta[12]annulen-8-yl pyridine-3-carboxylic acid	Generator

Chemical Formula

C₃₈H₄₉NO₁₄

Average Mass

743.8030 Da

Monoisotopic Mass

743.31531 Da

IUPAC Name

7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1H,2H,3H,3aH,4H,5H,6H,7H,8H,9H,12H,13H,13aH-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate

Traditional Name

7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1H,2H,3H,3aH,4H,6H,7H,8H-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate

CAS Registry Number

Not Available

SMILES

CC=C(C)C(=O)OC1C(OC(C)=O)C(OC(=O)C2=CC=CN=C2)C(C)(C)C=CC(C)(O)C(=O)C2(O)CC(C)C(OC(=O)C(=C)C(C)OO)C2C(O)C1=C

InChI Identifier

InChI=1S/C38H49NO14/c1-11-19(2)32(42)51-29-22(5)27(41)26-28(50-33(43)21(4)23(6)53-48)20(3)17-38(26,47)35(45)37(10,46)15-14-36(8,9)31(30(29)49-24(7)40)52-34(44)25-13-12-16-39-18-25/h11-16,18,20,23,26-31,41,46-48H,4-5,17H2,1-3,6-10H3

InChI Key

UYWMRBXGOAEPNN-UHFFFAOYSA-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
Euphorbia amygdaloides	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as jatrophane and cyclojatrophane diterpenoids. These are diterpenoids with a structure based on the jatrophane or the 9,13-jatrophane skeleton. Jatrophane can be derived from casbane by 6,10-cyclization and opening of the cyclopropane. Cyclojatrophane diterpenoids are based on the 9,13-cyclization of the jatrophane skeleton yields the 9,13-cyclojatrophane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Jatrophane and cyclojatrophane diterpenoids

Alternative Parents

Substituents

Jatrophane diterpenoid
Tetracarboxylic acid or derivatives
Pyridine carboxylic acid
Pyridine carboxylic acid or derivatives
Fatty acid ester
Acyloin
Pyridine
Fatty acyl
Cyclic alcohol
Heteroaromatic compound
Tertiary alcohol
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Carboxylic acid ester
Ketone
Hydroperoxide
Secondary alcohol
Polyol
Peroxol
Carboxylic acid derivative
Organoheterocyclic compound
Alkyl hydroperoxide
Azacycle
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Organic oxide
Organic oxygen compound
Alcohol
Organopnictogen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	2.44	ALOGPS
logP	4.19	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	11.62	ChemAxon
pKa (Strongest Basic)	3.24	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	225.31 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	187.4 m³·mol⁻¹	ChemAxon
Polarizability	74.65 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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate (NP0280381)

MOL for NP0280381 (7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate)

3D MOL for NP0280381 (7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate)

3D SDF for NP0280381 (7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate)

3D-SDF for NP0280381 (7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate)

PDB for NP0280381 (7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate)

3D PDB for NP0280381 (7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate)

SMILES for NP0280381 (7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate)

INCHI for NP0280381 (7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate)

Structure for NP0280381 (7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate)

3D Structure for NP0280381 (7-(acetyloxy)-3-[(3-hydroperoxy-2-methylidenebutanoyl)oxy]-4,12,13a-trihydroxy-2,9,9,12-tetramethyl-6-[(2-methylbut-2-enoyl)oxy]-5-methylidene-13-oxo-1h,2h,3h,3ah,4h,6h,7h,8h-cyclopenta[12]annulen-8-yl pyridine-3-carboxylate)