NP-MRD: Showing NP-Card for 1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate (NP0280543)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-09 06:23:39 UTC

Updated at

2022-09-09 06:23:40 UTC

NP-MRD ID

NP0280543

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate

Description

1,3-Dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate belongs to the class of organic compounds known as endocannabinoids. These are arachidonic acid derivatives containing either an N-acetylethanolamine(type 1) or a glycerol(types 2 and 3) moiety attached to the aliphatic tail. 1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate is found in Paulownia tomentosa. 1,3-Dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261501362D          

 32 31  0  0  0  0            999 V2000
   -0.1855  -13.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5634  -13.0993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9865  -13.2290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6605  -13.7047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4095  -13.3587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0836  -13.8344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8326  -13.4885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5066  -13.9641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2556  -13.6182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9297  -14.0938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6786  -13.7479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3527  -14.2236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2778  -15.0452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1017  -13.8776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7757  -14.3533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5247  -14.0074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1988  -14.4830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9478  -14.1371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6218  -14.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3708  -14.2668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4457  -13.4452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0449  -14.7425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7938  -14.3965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4679  -14.8722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2169  -14.5263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.8687  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6177  -13.2290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0227  -13.3155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3486  -12.8398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5996  -13.1858    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4235  -12.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  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  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 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
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 19 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END

     RDKit          3D

 80 79  0  0  0  0  0  0  0  0999 V2000
    6.2407   -2.7796    3.5872 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7399   -1.4135    3.9947 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5531   -0.7838    2.8842 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7255   -0.6182    1.6159 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5373    0.2509    1.8403 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6765    0.4107    0.5635 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4577    1.0212   -0.5274 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8790    1.2664   -1.8440 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7996    2.2364   -2.0430 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5522    1.9948   -1.3025 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4553    3.0056   -1.6864 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1123    2.9502   -3.1324 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6097    1.6171   -3.6050 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3109    1.6537   -4.9831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6930    1.2683   -2.9194 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1948   -0.0768   -3.4063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4847   -0.4316   -2.7317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3368   -0.5181   -1.2251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7262   -0.8873   -0.6943 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7103   -1.0036    0.8007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0291   -1.3581    1.3347 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0733   -1.5546    0.6662 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2466   -1.5170    2.7220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4696   -1.8497    3.2669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5009   -3.1359    4.0436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1479   -4.2265    3.2504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9541   -0.7114    4.1251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0646    0.4097    3.2796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6608    0.1141   -1.0484 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7519   -0.0711   -1.8613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6574    1.0683   -2.1456 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9683   -1.1924   -2.3499 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3261   -3.4669    4.4305 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1954   -2.6757    3.2141 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8221   -3.1821    2.7312 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8536   -0.7866    4.2562 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3961   -1.5464    4.8783 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3892   -1.4614    2.6442 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9633    0.1880    3.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4344   -1.5974    1.2235 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4176   -0.1212    0.8980 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8510   -0.1149    2.6158 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8279    1.2896    2.1224 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3695   -0.6238    0.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7833    0.9172    0.9270 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3508    0.3342   -0.6939 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9886    1.9708   -0.1594 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5683    0.2432   -2.3167 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7169    1.5714   -2.5881 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5777    2.2429   -3.1663 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2362    3.2606   -1.7949 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7498    2.3016   -0.2226 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2360    0.9716   -1.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7657    4.0218   -1.3820 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5715    2.7356   -1.0840 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9319    3.2548   -3.8044 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3101    3.7286   -3.2954 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3225    0.8050   -3.3995 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6195    2.5185   -5.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4586    1.1686   -1.8234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4293    2.0653   -3.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4120   -0.8407   -3.1499 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2886   -0.0965   -4.5076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9142   -1.3532   -3.1571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2177    0.3852   -3.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1091    0.4704   -0.7789 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6260   -1.3071   -0.9844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0449   -1.8525   -1.1263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3609   -0.0176    1.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9905   -1.7748    1.1531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2121   -1.9616    2.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9620   -3.0944    4.9978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5826   -3.3076    4.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8802   -4.3729    2.5883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9757   -0.9525    4.5225 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2679   -0.4286    4.9259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0964    1.2510    3.8016 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9928    1.5171   -1.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5735    0.7031   -2.6530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1590    1.8819   -2.7177 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  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 24 27  1  0
 27 28  1  0
 19 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  2  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  5 42  1  0
  5 43  1  0
  6 44  1  0
  6 45  1  0
  7 46  1  0
  7 47  1  0
  8 48  1  0
  8 49  1  0
  9 50  1  0
  9 51  1  0
 10 52  1  0
 10 53  1  0
 11 54  1  0
 11 55  1  0
 12 56  1  0
 12 57  1  0
 13 58  1  6
 14 59  1  0
 15 60  1  0
 15 61  1  0
 16 62  1  0
 16 63  1  0
 17 64  1  0
 17 65  1  0
 18 66  1  0
 18 67  1  0
 19 68  1  6
 20 69  1  0
 20 70  1  0
 24 71  1  0
 25 72  1  0
 25 73  1  0
 26 74  1  0
 27 75  1  0
 27 76  1  0
 28 77  1  0
 31 78  1  0
 31 79  1  0
 31 80  1  0
M  END


  Mrv1533004261501362D          

 32 31  0  0  0  0            999 V2000
   -0.1855  -13.4452    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5634  -13.0993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9865  -13.2290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6605  -13.7047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4095  -13.3587    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0836  -13.8344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8326  -13.4885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5066  -13.9641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2556  -13.6182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9297  -14.0938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6786  -13.7479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3527  -14.2236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2778  -15.0452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1017  -13.8776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7757  -14.3533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5247  -14.0074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1988  -14.4830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9478  -14.1371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6218  -14.6128    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3708  -14.2668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4457  -13.4452    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0449  -14.7425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7938  -14.3965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4679  -14.8722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2169  -14.5263    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.8687  -13.5749    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6177  -13.2290    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0227  -13.3155    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.3486  -12.8398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5996  -13.1858    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4235  -12.0182    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  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  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 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
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 19 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0280543

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCC(O)CCCCC(CC(=O)OC(CO)CO)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C25H48O7/c1-3-4-5-6-7-8-9-10-11-12-15-22(29)16-13-14-17-23(31-21(2)28)18-25(30)32-24(19-26)20-27/h22-24,26-27,29H,3-20H2,1-2H3

> <INCHI_KEY>
NOSVWQDVCCYURV-UHFFFAOYSA-N

> <FORMULA>
C25H48O7

> <MOLECULAR_WEIGHT>
460.652

> <EXACT_MASS>
460.340003886

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
56.356491296413395

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate

> <ALOGPS_LOGP>
5.10

> <JCHEM_LOGP>
4.683910356

> <ALOGPS_LOGS>
-4.84

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.979617396788388

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.278370867040358

> <JCHEM_PKA_STRONGEST_BASIC>
-1.2748214278476668

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
124.84799999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
24

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.67e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      -0.346 -25.098   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.052 -24.452   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.310 -25.340   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.708 -24.694   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.966 -25.582   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.364 -24.936   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.623 -25.824   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.021 -25.178   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.279 -26.066   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.677 -25.421   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.935 -26.309   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.333 -25.663   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.592 -26.551   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      15.452 -28.084   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      16.990 -25.905   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      18.248 -26.793   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      19.646 -26.147   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.904 -27.035   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      22.302 -26.389   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      23.561 -27.277   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      24.959 -26.631   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      25.099 -25.098   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      26.217 -27.519   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      27.615 -26.874   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      28.873 -27.761   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      30.272 -27.116   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      27.755 -25.340   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      29.153 -24.694   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      22.442 -24.856   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      21.184 -23.968   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      19.786 -24.613   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      21.324 -22.434   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
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                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   29                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28                                                       
CONECT   28   27                                                            
CONECT   29   19   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   62    0
END

View in JSmol

Synonyms

Value	Source
1,3-Dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoic acid	Generator

Chemical Formula

C₂₅H₄₈O₇

Average Mass

460.6520 Da

Monoisotopic Mass

460.34000 Da

IUPAC Name

1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate

Traditional Name

1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCC(O)CCCCC(CC(=O)OC(CO)CO)OC(C)=O

InChI Identifier

InChI=1S/C25H48O7/c1-3-4-5-6-7-8-9-10-11-12-15-22(29)16-13-14-17-23(31-21(2)28)18-25(30)32-24(19-26)20-27/h22-24,26-27,29H,3-20H2,1-2H3

InChI Key

NOSVWQDVCCYURV-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
Paulownia tomentosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as endocannabinoids. These are arachidonic acid derivatives containing either an N-acetylethanolamine(type 1) or a glycerol(types 2 and 3) moiety attached to the aliphatic tail.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Endocannabinoids

Sub Class

Not Available

Direct Parent

Endocannabinoids

Alternative Parents

Substituents

2-arachidonoylglycerol-skeleton
Long chain fatty alcohol
Fatty alcohol ester
Fatty alcohol
2-acyl-sn-glycerol
Monoradylglycerol
Monoacylglycerol
Fatty acid ester
Glycerolipid
Fatty acyl
Dicarboxylic acid or derivatives
Secondary alcohol
Carboxylic acid ester
Carboxylic acid derivative
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Carbonyl group
Organooxygen compound
Primary alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	5.1	ALOGPS
logP	4.68	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	14.28	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	24	ChemAxon
Refractivity	124.85 m³·mol⁻¹	ChemAxon
Polarizability	56.36 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

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 1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate (NP0280543)

MOL for NP0280543 (1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate)

3D MOL for NP0280543 (1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate)

3D SDF for NP0280543 (1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate)

3D-SDF for NP0280543 (1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate)

PDB for NP0280543 (1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate)

3D PDB for NP0280543 (1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate)

SMILES for NP0280543 (1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate)

INCHI for NP0280543 (1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate)

Structure for NP0280543 (1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate)

3D Structure for NP0280543 (1,3-dihydroxypropan-2-yl 3-(acetyloxy)-8-hydroxyicosanoate)