NP-MRD: Showing NP-Card for Ardisiaquinone F (NP0075103)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 20:24:51 UTC

Updated at

2022-04-28 20:24:51 UTC

NP-MRD ID

NP0075103

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Ardisiaquinone F

Description

Ardisiaquinone F is found in Ardisia sieboldii and Ardisia sieboldii Miguel.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282222242D          

 36 37  0  0  0  0            999 V2000
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  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
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    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
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 O   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
   -4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 11 20  1  0  0  0  0
  1 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 32 34  1  0  0  0  0
 31 35  1  0  0  0  0
 30 36  1  0  0  0  0
M  END

     RDKit          3D

 78 79  0  0  0  0  0  0  0  0999 V2000
  -11.7450   -0.8024   -1.5149 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7806   -0.8512   -2.5515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4295   -0.9900   -2.1778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9800   -2.1216   -1.6610 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5884   -2.2828   -1.2691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2177   -3.3804   -0.7834 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6162   -1.1747   -1.4368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2747   -1.4163   -0.9786 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3250   -0.3346   -0.7505 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7646    0.5615    0.3842 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8197    1.7196    0.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4708    1.1761    0.9617 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5638    2.3923    1.1979 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1783    1.8063    1.5436 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2805    1.0052    0.4320 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5611   -0.2700    0.4962 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4588   -1.0797    1.6814 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6948   -1.7813    2.0971 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8871   -0.9881    2.4538 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4966   -0.1498    1.3630 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7481    0.5649    1.8746 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8236   -0.3237    2.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4378   -1.2622    1.3758 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1066   -0.6448    0.2334 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4502   -0.2782    0.3408 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1052    0.2993   -0.7232 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4588    0.6604   -0.5905 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4477    0.5238   -1.9068 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1988    1.1505   -3.0236 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1300    0.1721   -2.0348 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4690    0.4002   -3.2315 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4620   -0.4147   -0.9553 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0939   -0.0707   -1.9515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2545    0.9918   -2.1382 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4863    0.1020   -2.3471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8776    1.1870   -2.8332 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.7132   -1.7283   -0.9158 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7593   -0.6670   -1.8963 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4475    0.0248   -0.8100 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7166   -2.9269   -1.5462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3075   -2.0477   -0.0328 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8160   -2.1529   -1.7150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3618   -0.8058   -0.3808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0045    0.2387   -1.6417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8284    0.8240    0.4068 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6579   -0.0469    1.3600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8016    2.4373   -0.2149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2214    2.2715    1.4987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0131    0.6236    0.1287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5505    0.6105    1.9008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8750    2.9530    2.1034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5118    3.0011    0.2950 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4812    2.7316    1.6096 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3090    1.3464    2.5159 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4045    1.5011   -0.5454 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9089   -0.7876   -0.4309 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1024   -0.5221    2.5949 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3628   -1.8516    1.4717 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3974   -2.3503    3.0571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9559   -2.5952    1.3405 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6186   -0.2867    3.3188 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6802   -1.6356    2.9447 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8038    0.6873    1.1519 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6415   -0.6836    0.4291 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3930    1.1658    2.7515 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0330    1.2912    1.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6635    0.3464    2.7085 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5222   -0.8618    3.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2270   -1.8371    1.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7476   -2.0456    1.0012 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9221   -0.4728    1.2840 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9354    0.4951    0.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5662    1.8801   -3.5794 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6438    0.3768   -3.6940 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0210    1.7469   -2.5843 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8935    0.8114   -4.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4102   -0.6803   -1.1128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4651    1.9512   -1.9016 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  2  0
  7 33  2  0
 33 34  1  0
 33 35  1  0
 35 36  2  0
 35  3  1  0
 32 24  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
  4 40  1  0
  8 41  1  0
  8 42  1  0
  9 43  1  0
  9 44  1  0
 10 45  1  0
 10 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  0
 12 50  1  0
 13 51  1  0
 13 52  1  0
 14 53  1  0
 14 54  1  0
 15 55  1  0
 16 56  1  0
 17 57  1  0
 17 58  1  0
 18 59  1  0
 18 60  1  0
 19 61  1  0
 19 62  1  0
 20 63  1  0
 20 64  1  0
 21 65  1  0
 21 66  1  0
 22 67  1  0
 22 68  1  0
 23 69  1  0
 23 70  1  0
 25 71  1  0
 27 72  1  0
 29 73  1  0
 29 74  1  0
 29 75  1  0
 31 76  1  0
 32 77  1  0
 34 78  1  0
M  END


  Mrv1652304282222242D          

 36 37  0  0  0  0            999 V2000
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.1250    0.0000 C   0  0  0  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
   -4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    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
   -2.8579   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 O   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
   -4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 14 18  1  0  0  0  0
 18 19  1  0  0  0  0
 11 20  1  0  0  0  0
  1 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 28 33  1  0  0  0  0
 32 34  1  0  0  0  0
 31 35  1  0  0  0  0
 30 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0075103

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=O)C(CCCCCCC\C=C/CCCCCCCC2=CC(O)=C(C)C(O)=C2)=C(O)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H42O6/c1-22-25(31)19-23(20-26(22)32)17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-24-27(33)21-28(36-2)30(35)29(24)34/h3-4,19-21,31-32,34H,5-18H2,1-2H3/b4-3-

> <INCHI_KEY>
GOFXYNRKBQYGLK-ARJAWSKDSA-N

> <FORMULA>
C30H42O6

> <MOLECULAR_WEIGHT>
498.66

> <EXACT_MASS>
498.298139072

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
58.690600153615435

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(8Z)-16-(3,5-dihydroxy-4-methylphenyl)hexadec-8-en-1-yl]-3-hydroxy-5-methoxycyclohexa-2,5-diene-1,4-dione

> <ALOGPS_LOGP>
7.18

> <JCHEM_LOGP>
8.286448029333332

> <ALOGPS_LOGS>
-6.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.755948979778596

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.579417319091517

> <JCHEM_PKA_STRONGEST_BASIC>
-4.954174398412312

> <JCHEM_POLAR_SURFACE_AREA>
104.06000000000002

> <JCHEM_REFRACTIVITY>
147.9025

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.19e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(8Z)-16-(3,5-dihydroxy-4-methylphenyl)hexadec-8-en-1-yl]-3-hydroxy-5-methoxycyclohexa-2,5-diene-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0     -10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0     -10.669  -4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0     -12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      14.670 -10.010   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      16.004  -9.240   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      17.338 -10.010   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.670 -11.550   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      16.004 -13.860   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      18.672 -12.320   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      18.672  -9.240   0.000  0.00  0.00           O+0
CONECT    1    2   21                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12   20                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   10   17                                                  
CONECT   17   16                                                            
CONECT   18   14   19                                                       
CONECT   19   18                                                            
CONECT   20   11                                                            
CONECT   21    1   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31   36                                                  
CONECT   31   30   32   35                                                  
CONECT   32   31   33   34                                                  
CONECT   33   32   28                                                       
CONECT   34   32                                                            
CONECT   35   31                                                            
CONECT   36   30                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₂O₆

Average Mass

498.6600 Da

Monoisotopic Mass

498.29814 Da

IUPAC Name

2-[(8Z)-16-(3,5-dihydroxy-4-methylphenyl)hexadec-8-en-1-yl]-3-hydroxy-5-methoxycyclohexa-2,5-diene-1,4-dione

Traditional Name

2-[(8Z)-16-(3,5-dihydroxy-4-methylphenyl)hexadec-8-en-1-yl]-3-hydroxy-5-methoxycyclohexa-2,5-diene-1,4-dione

CAS Registry Number

Not Available

SMILES

COC1=CC(=O)C(CCCCCCC\C=C/CCCCCCCC2=CC(O)=C(C)C(O)=C2)=C(O)C1=O

InChI Identifier

InChI=1S/C30H42O6/c1-22-25(31)19-23(20-26(22)32)17-15-13-11-9-7-5-3-4-6-8-10-12-14-16-18-24-27(33)21-28(36-2)30(35)29(24)34/h3-4,19-21,31-32,34H,5-18H2,1-2H3/b4-3-

InChI Key

GOFXYNRKBQYGLK-ARJAWSKDSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Ardisia sieboldii	LOTUS Database	35616633
Ardisia sieboldii Miguel	Plant	KNApSAcK

Chemical Taxonomy

Classification

Not classified

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	7.18	ALOGPS
logP	8.29	ChemAxon
logS	-6.1	ALOGPS
pKa (Strongest Acidic)	5.58	ChemAxon
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	104.06 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	147.9 m³·mol⁻¹	ChemAxon
Polarizability	58.69 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Not Available

Showing NP-Card for Ardisiaquinone F (NP0075103)

MOL for NP0075103 (Ardisiaquinone F)

3D MOL for NP0075103 (Ardisiaquinone F)

3D SDF for NP0075103 (Ardisiaquinone F)

3D-SDF for NP0075103 (Ardisiaquinone F)

PDB for NP0075103 (Ardisiaquinone F)

3D PDB for NP0075103 (Ardisiaquinone F)

SMILES for NP0075103 (Ardisiaquinone F)

INCHI for NP0075103 (Ardisiaquinone F)

Structure for NP0075103 (Ardisiaquinone F)

3D Structure for NP0075103 (Ardisiaquinone F)