NP-MRD: Showing NP-Card for 1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate (NP0194241)

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Record Information

Version

2.0

Created at

2022-09-04 11:52:12 UTC

Updated at

2022-09-04 11:52:12 UTC

NP-MRD ID

NP0194241

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate

Description

1-{[6-(Aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate belongs to the class of organic compounds known as glycosyldiacylglycerols. These are diacylglycerols that carry a saccharide moiety linked to the glycerol. 1-{[6-(Aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate is a very strong basic compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251515152D          

 49 49  0  0  0  0            999 V2000
  -10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   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
    4.2868   -2.4750    0.0000 C   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
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    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
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 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  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
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 22 31  1  0  0  0  0
 31 32  1  0  0  0  0
 19 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  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
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
M  END

     RDKit          3D

124124  0  0  0  0  0  0  0  0999 V2000
    0.4285    2.1500    3.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7772    1.4592    2.9785 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6066   -0.0148    3.1274 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8567   -0.6935    2.0402 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5203   -0.5988    0.6980 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7354   -1.3830   -0.3354 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4208   -1.3667   -1.6727 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7160   -2.1665   -2.6970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6206   -1.6995   -3.1722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5165   -0.3716   -3.9031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8041    0.0809   -4.4901 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9228    0.3473   -3.5562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1495    0.7148   -4.3917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3067    1.0096   -3.4071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4599   -0.2043   -2.5432 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0764   -1.1841   -2.9861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9114   -0.2254   -1.2745 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9787   -1.3286   -0.4202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2271   -0.8787    0.9087 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2343   -2.0453    1.8129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6297   -2.0927    2.8710 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0282   -2.0964    3.9831 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6943   -2.3495    4.0720 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1345   -2.0885    5.2712 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2337   -2.7997    5.4020 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0402   -4.2546    5.2861 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8773   -2.4274    6.5147 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7038   -1.4123    7.4516 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3687   -2.6194    6.3346 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.9873   -1.3678    6.4497 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6651   -3.1634    4.9611 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0608   -4.3777    4.8253 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9632   -0.4589    0.4191 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7435    0.9066    0.2306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7278    1.6681    0.5421 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5289    1.5565   -0.2885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8100    3.0091   -0.6145 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7044    3.8110   -1.1574 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4905    4.0295   -0.2936 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5028    4.9074   -0.9678 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0558    4.3042   -2.1891 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8350    3.0258   -1.8753 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4163    2.4366   -3.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2050    1.2442   -2.7888 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8609    0.4937   -3.8962 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8359    1.2650   -4.7035 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3984    0.3233   -5.7715 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3886    1.1463   -6.5749 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0313    0.3310   -7.6756 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4723    3.0369    2.3760 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3413    2.5660    4.0821 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4063    1.4770    2.8133 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2135    1.6646    1.9767 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4161    1.8108    3.8011 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6123   -0.4806    3.1962 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0283   -0.2062    4.0869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1878   -0.3232    1.8972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7337   -1.7689    2.3056 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6952    0.4395    0.3825 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5144   -1.1123    0.8029 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6993   -2.4577   -0.0274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2737   -1.0229   -0.4193 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4312   -0.2939   -2.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4970   -1.6148   -1.5680 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5248   -3.2278   -2.2977 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3943   -2.4045   -3.5820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2833   -1.5760   -2.2862 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1272   -2.3940   -3.8402 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2002   -0.5426   -4.7350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0694    0.3533   -3.2203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5807    1.0633   -5.0115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0713   -0.6269   -5.3117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6713    1.2278   -2.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2038   -0.4866   -2.9091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4510   -0.0800   -5.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9800    1.6558   -4.9411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1919    1.1888   -4.0196 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0242    1.8954   -2.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3947   -2.1537   -0.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9808   -1.6236   -0.1284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8193   -0.0408    1.2317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0151   -2.9382    1.0611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4033   -2.2118    1.9783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2515   -1.1506    4.5737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8643   -0.9942    5.3129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8900   -2.4492    4.5917 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6861   -2.5241    6.3648 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0316   -4.6371    5.2192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3263   -4.3877    4.2991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4311   -3.3464    7.0158 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7374   -3.2487    7.1495 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2199   -1.1782    7.3986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7378   -3.2212    4.7967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7921   -4.6306    3.9179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1079    1.0279   -1.1743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7461    1.5251    0.4837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6346    3.0072   -1.3841 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3013    3.5148    0.2666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1280    4.8404   -1.3811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3795    3.4199   -2.1587 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1393    4.5864    0.6326 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9698    3.0942    0.0318 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2721    5.2610   -0.2430 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9288    5.8359   -1.2844 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8286    4.9645   -2.6917 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3178    4.1114   -2.9870 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2352    2.2917   -1.3377 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6800    3.3547   -1.2129 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5434    2.2311   -3.8120 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0496    3.1833   -3.6605 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9996    1.6146   -2.0615 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6039    0.5528   -2.1793 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1137    0.0182   -4.5641 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4278   -0.3530   -3.4218 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4064    2.1120   -5.2631 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7270    1.5632   -4.0823 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8429   -0.5756   -5.3487 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5339    0.1176   -6.4657 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1307    1.5559   -5.8637 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8979    2.0112   -7.0648 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3811    0.2959   -8.5742 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2705   -0.6916   -7.3821 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9572    0.8607   -8.0217 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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 29 30  1  0
 29 31  1  0
 31 32  1  0
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 33 34  1  0
 34 35  2  0
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 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 31 22  1  0
  1 50  1  0
  1 51  1  0
  1 52  1  0
  2 53  1  0
  2 54  1  0
  3 55  1  0
  3 56  1  0
  4 57  1  0
  4 58  1  0
  5 59  1  0
  5 60  1  0
  6 61  1  0
  6 62  1  0
  7 63  1  0
  7 64  1  0
  8 65  1  0
  8 66  1  0
  9 67  1  0
  9 68  1  0
 10 69  1  0
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 11 71  1  0
 11 72  1  0
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 12 74  1  0
 13 75  1  0
 13 76  1  0
 14 77  1  0
 14 78  1  0
 18 79  1  0
 18 80  1  0
 19 81  1  1
 20 82  1  0
 20 83  1  0
 22 84  1  1
 24 85  1  6
 25 86  1  0
 25 87  1  0
 26 88  1  0
 26 89  1  0
 27 90  1  1
 28 91  1  0
 29 92  1  1
 30 93  1  0
 31 94  1  6
 32 95  1  0
 36 96  1  0
 36 97  1  0
 37 98  1  0
 37 99  1  0
 38100  1  0
 38101  1  0
 39102  1  0
 39103  1  0
 40104  1  0
 40105  1  0
 41106  1  0
 41107  1  0
 42108  1  0
 42109  1  0
 43110  1  0
 43111  1  0
 44112  1  0
 44113  1  0
 45114  1  0
 45115  1  0
 46116  1  0
 46117  1  0
 47118  1  0
 47119  1  0
 48120  1  0
 48121  1  0
 49122  1  0
 49123  1  0
 49124  1  0
M  END


  Mrv1533004251515152D          

 49 49  0  0  0  0            999 V2000
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  -10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   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
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   -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 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   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
    4.2868   -2.4750    0.0000 C   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
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7171   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4315   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1460   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8605   -2.4750    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
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 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  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
 24 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 22 31  1  0  0  0  0
 31 32  1  0  0  0  0
 19 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  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
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0194241

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCC(=O)OCC(COC1OC(CN)C(O)C(O)C1O)OC(=O)CCCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C39H75NO9/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-34(41)46-30-32(31-47-39-38(45)37(44)36(43)33(29-40)49-39)48-35(42)28-26-24-22-20-18-16-14-12-10-8-6-4-2/h32-33,36-39,43-45H,3-31,40H2,1-2H3

> <INCHI_KEY>
QNPIEBGHSXVAOA-UHFFFAOYSA-N

> <FORMULA>
C39H75NO9

> <MOLECULAR_WEIGHT>
702.027

> <EXACT_MASS>
701.544182999

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
124

> <JCHEM_AVERAGE_POLARIZABILITY>
86.74557570585432

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate

> <ALOGPS_LOGP>
7.22

> <JCHEM_LOGP>
9.236239009666665

> <ALOGPS_LOGS>
-6.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.239127759304953

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.217927287668118

> <JCHEM_PKA_STRONGEST_BASIC>
8.7961535819243

> <JCHEM_POLAR_SURFACE_AREA>
157.76999999999998

> <JCHEM_REFRACTIVITY>
192.5677

> <JCHEM_ROTATABLE_BOND_COUNT>
35

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.36e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0     -20.005  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -18.672  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -17.338  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -16.004  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -14.670  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -13.337  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -12.003  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -10.669  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.000  -0.000   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   26  N   UNK     0      -1.334   3.850   0.000  0.00  0.00           N+0
HETATM   27  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      17.338  -5.390   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      20.005  -5.390   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      21.339  -4.620   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      22.673  -5.390   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      24.006  -4.620   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                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   33                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   31                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   27                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   24   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   22   32                                                  
CONECT   32   31                                                            
CONECT   33   19   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48                                                            
MASTER        0    0    0    0    0    0    0    0   49    0   98    0
END

View in JSmol

Synonyms

Value	Source
1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoic acid	Generator

Chemical Formula

C₃₉H₇₅NO₉

Average Mass

702.0270 Da

Monoisotopic Mass

701.54418 Da

IUPAC Name

1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate

Traditional Name

1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCC(=O)OCC(COC1OC(CN)C(O)C(O)C1O)OC(=O)CCCCCCCCCCCCCC

InChI Identifier

InChI=1S/C39H75NO9/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-34(41)46-30-32(31-47-39-38(45)37(44)36(43)33(29-40)49-39)48-35(42)28-26-24-22-20-18-16-14-12-10-8-6-4-2/h32-33,36-39,43-45H,3-31,40H2,1-2H3

InChI Key

QNPIEBGHSXVAOA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glycosyldiacylglycerols. These are diacylglycerols that carry a saccharide moiety linked to the glycerol.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerolipids

Sub Class

Glycosylglycerols

Direct Parent

Glycosyldiacylglycerols

Alternative Parents

Substituents

Glycosyldiacylglycerol
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Glycosyl compound
O-glycosyl compound
Fatty acid ester
Amino saccharide
Dicarboxylic acid or derivatives
Fatty acyl
Monosaccharide
Oxane
Amino acid or derivatives
Carboxylic acid ester
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Polyol
Amine
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Alcohol
Carbonyl group
Primary aliphatic amine
Primary amine
Organic nitrogen compound
Organonitrogen compound
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	7.22	ALOGPS
logP	9.24	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Acidic)	12.22	ChemAxon
pKa (Strongest Basic)	8.8	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	157.77 Å²	ChemAxon
Rotatable Bond Count	35	ChemAxon
Refractivity	192.57 m³·mol⁻¹	ChemAxon
Polarizability	86.75 Å³	ChemAxon
Number of Rings	1	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

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-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate (NP0194241)

MOL for NP0194241 (1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate)

3D MOL for NP0194241 (1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate)

3D SDF for NP0194241 (1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate)

3D-SDF for NP0194241 (1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate)

PDB for NP0194241 (1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate)

3D PDB for NP0194241 (1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate)

SMILES for NP0194241 (1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate)

INCHI for NP0194241 (1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate)

Structure for NP0194241 (1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate)

3D Structure for NP0194241 (1-{[6-(aminomethyl)-3,4,5-trihydroxyoxan-2-yl]oxy}-3-(pentadecanoyloxy)propan-2-yl pentadecanoate)