NP-MRD: Showing NP-Card for (2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid (NP0165247)

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Record Information

Version

2.0

Created at

2022-09-03 00:19:11 UTC

Updated at

2022-09-03 00:19:11 UTC

NP-MRD ID

NP0165247

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid

Description

ASTERIACEREBROSIDE G belongs to the class of organic compounds known as glycosyl-n-acylsphingosines. Glycosyl-N-acylsphingosines are compounds containing a sphingosine linked to a simple glucosyl moiety. (2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid is found in Asterias amurensis. (2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid was first documented in 2006 (PMID: 16872149). Based on a literature review very few articles have been published on ASTERIACEREBROSIDE G.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032202192D          

 52 52  0  0  1  0            999 V2000
   -9.2881    3.7125    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
  -10.0026    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7171    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4315   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4315   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1460   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1460   -2.0625    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
  -10.7171   -2.0625    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   -2.0625    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   -2.0625    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   -2.0625    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   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -6.1875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5724   -7.0125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -5.7750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.0013   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0013   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.0625    0.0000 N   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   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.0625    0.0000 C   0  0  2  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   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.0625    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
    2.1434   -2.0625    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
    3.5724   -2.0625    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   -2.0625    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   -2.0625    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  2  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  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  6  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  6  0  0  0
 28 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
 32 33  1  6  0  0  0
 32 34  1  0  0  0  0
 25 34  1  0  0  0  0
 34 35  1  1  0  0  0
 22 36  1  1  0  0  0
 36 37  2  0  0  0  0
 37 38  1  4  0  0  0
 37 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 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
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
M  END

     RDKit          3D

131131  0  0  0  0  0  0  0  0999 V2000
   -1.4449    5.8886   -2.4902 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7476    4.4846   -2.9662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6485    4.3256   -4.4583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2375    4.7228   -4.9215 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2001    4.5901   -6.4556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3874    3.2136   -6.9119 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5546    2.1520   -6.7642 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2740    1.5762   -5.6637 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5573    1.1128   -4.5067 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8976    1.3974   -3.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0209    2.1972   -2.7697 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6913    3.3152   -1.8616 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8981    4.0788   -1.3670 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9367    3.3651   -0.6568 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7774    2.6412    0.5997 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3536    3.3013    1.8341 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9735    3.8472    1.9714 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9122    2.7852    1.9470 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1126    2.5894    2.9884 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9632    1.6253    3.1602 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2391    2.3169    3.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0608    0.4563    2.2772 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0040   -0.5470    2.1799 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4226   -1.2776    3.2221 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9926   -0.7993    4.3320 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3644   -1.2092    4.4467 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8880   -0.3539    5.4195 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3941   -0.3718    5.4716 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7749    0.5258    6.4808 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3288   -0.6364    6.7939 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8756    0.3325    7.6536 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8202   -0.4019    6.7244 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2022   -0.7202    7.9179 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2828   -1.2345    5.6075 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0637   -1.0617    5.4571 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3748    1.0157    0.9173 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5480    0.7573    0.3822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3787   -0.0418    1.1842 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9671    1.2323   -0.8867 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.3090    1.8060   -0.6554 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1013    0.5860   -2.1683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0243   -0.5058   -2.4756 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7679   -1.8930   -2.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4055   -2.4157   -0.8255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3772   -3.9669   -0.9376 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8766   -4.6416    0.2824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3784   -4.4229    0.5369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6122   -5.0221   -0.6416 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8530   -4.8975   -0.4595 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2824   -3.4659   -0.3430 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8036   -3.3440   -0.1893 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1533   -1.8540   -0.0850 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4530    5.9160   -1.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3875    6.6172   -3.2989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1869    6.2395   -1.7189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8284    4.2635   -2.6396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1644    3.7746   -2.3728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3783    5.0020   -4.9380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8587    3.2533   -4.6938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0863    5.7577   -4.5943 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4430    3.9699   -4.4889 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7439    5.0777   -6.7567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0237    5.2303   -6.8274 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6178    3.2754   -8.0596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4378    2.9020   -6.5651 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0414    1.2167   -7.2965 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3933    2.2786   -7.6082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2294    2.1392   -5.4006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7759    0.6088   -6.0883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3297    0.4799   -4.6743 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2208    0.9549   -2.4894 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7127    1.4411   -2.2939 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6725    2.6063   -3.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0750    2.9434   -1.0283 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0453    4.0386   -2.3935 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5337    5.0243   -0.9153 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3721    4.4757   -2.3367 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4794    2.6274   -1.3703 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8308    4.0817   -0.4784 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7788    2.1034    0.7818 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1054    1.7150    0.4919 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4169    2.5056    2.6602 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1212    4.0411    2.2284 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6602    4.5746    1.2066 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8824    4.4329    2.9364 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7525    2.1558    1.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3372    3.2927    3.8345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9762    1.2932    4.2436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2882    2.9530    3.8293 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0156   -0.1320    2.5165 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9244   -0.0155    1.7829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2585   -1.2290    1.2882 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0664    0.2944    4.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6091    0.7177    5.1928 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7951    0.0286    4.5320 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7729   -1.3625    5.7527 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1948    1.3408    6.1338 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5650   -1.6449    7.1672 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3784   -0.0833    8.3989 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6788    0.6763    6.5548 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8456   -1.0817    8.6003 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5721   -2.2976    5.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5674   -1.6643    6.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309032202192D          

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M  END
> <DATABASE_ID>
NP0165247

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCC[C@@H](O)C(O)=N[C@@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H](O)\C=C\CCCCCCC\C=C/CCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C42H79NO9/c1-3-5-7-9-11-13-15-16-17-18-19-20-21-23-24-26-28-30-35(45)34(33-51-42-40(49)39(48)38(47)37(32-44)52-42)43-41(50)36(46)31-29-27-25-22-14-12-10-8-6-4-2/h16-17,28,30,34-40,42,44-49H,3-15,18-27,29,31-33H2,1-2H3,(H,43,50)/b17-16-,30-28+/t34-,35+,36+,37+,38+,39-,40+,42+/m0/s1

> <INCHI_KEY>
MOQQBSZILUXXBS-OJKKOOKUSA-N

> <FORMULA>
C42H79NO9

> <MOLECULAR_WEIGHT>
742.092

> <EXACT_MASS>
741.575483128

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
131

> <JCHEM_AVERAGE_POLARIZABILITY>
91.96228239798364

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-2-hydroxy-N-[(2S,3R,4E,13Z)-3-hydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid

> <ALOGPS_LOGP>
7.12

> <JCHEM_LOGP>
9.570273377666668

> <ALOGPS_LOGS>
-5.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.203429815095161

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9752639564464554

> <JCHEM_PKA_STRONGEST_BASIC>
1.736658694015451

> <JCHEM_POLAR_SURFACE_AREA>
172.43

> <JCHEM_REFRACTIVITY>
210.52150000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
34

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.55e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-hydroxy-N-[(2S,3R,4E,13Z)-3-hydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0     -17.338   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -17.338   5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -18.672   4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -18.672   3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -20.005   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -20.005   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -21.339  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -21.339  -1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -22.673  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -22.673  -3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -21.339  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -20.005  -3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -17.338  -3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -14.670  -3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0     -12.003  -3.850   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -9.336  -3.850   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -9.336  -2.310   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -8.002  -6.160   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -6.668  -6.930   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -6.668  -8.470   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -5.335 -10.780   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -4.001 -13.090   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -6.668 -13.090   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -8.002 -10.780   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -9.336 -11.550   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -8.002  -9.240   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -9.336  -8.470   0.000  0.00  0.00           O+0
HETATM   36  N   UNK     0      -6.668  -3.850   0.000  0.00  0.00           N+0
HETATM   37  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      -5.335  -6.160   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      -4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -1.334  -3.850   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       1.334  -3.850   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       9.336  -3.850   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      12.003  -3.850   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                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   36                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   34                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   30                                                  
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   27   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   34                                                  
CONECT   33   32                                                            
CONECT   34   32   25   35                                                  
CONECT   35   34                                                            
CONECT   36   22   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   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   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51                                                            
MASTER        0    0    0    0    0    0    0    0   52    0  104    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₇₉NO₉

Average Mass

742.0920 Da

Monoisotopic Mass

741.57548 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC[C@@H](O)C(O)=N[C@@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)[C@H](O)\C=C\CCCCCCC\C=C/CCCCCCCC

InChI Identifier

InChI=1S/C42H79NO9/c1-3-5-7-9-11-13-15-16-17-18-19-20-21-23-24-26-28-30-35(45)34(33-51-42-40(49)39(48)38(47)37(32-44)52-42)43-41(50)36(46)31-29-27-25-22-14-12-10-8-6-4-2/h16-17,28,30,34-40,42,44-49H,3-15,18-27,29,31-33H2,1-2H3,(H,43,50)/b17-16-,30-28+/t34-,35+,36+,37+,38+,39-,40+,42+/m0/s1

InChI Key

MOQQBSZILUXXBS-OJKKOOKUSA-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
Asterias amurensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glycosyl-n-acylsphingosines. Glycosyl-N-acylsphingosines are compounds containing a sphingosine linked to a simple glucosyl moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Sphingolipids

Sub Class

Glycosphingolipids

Direct Parent

Glycosyl-N-acylsphingosines

Alternative Parents

Substituents

Glycosyl-n-acylsphingosine
Fatty acyl glycoside
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty amide
Fatty acyl
Monosaccharide
N-acyl-amine
Oxane
Carboxamide group
Secondary carboxylic acid amide
Secondary alcohol
Acetal
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Polyol
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Alcohol
Organic oxygen compound
Organic nitrogen compound
Primary alcohol
Carbonyl group
Organooxygen compound
Organonitrogen 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	7.12	ALOGPS
logS	-5.5	ALOGPS

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

10017790

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11843313

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Ishii T, Okino T, Mino Y: A ceramide and cerebroside from the starfish asterias amurensis Lutken and their plant-growth promotion activities. J Nat Prod. 2006 Jul;69(7):1080-2. doi: 10.1021/np050530e. [PubMed:16872149 ]
LOTUS database [Link]

Showing NP-Card for (2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid (NP0165247)

MOL for NP0165247 ((2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid)

3D MOL for NP0165247 ((2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid)

3D SDF for NP0165247 ((2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid)

3D-SDF for NP0165247 ((2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid)

PDB for NP0165247 ((2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid)

3D PDB for NP0165247 ((2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid)

SMILES for NP0165247 ((2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid)

INCHI for NP0165247 ((2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid)

Structure for NP0165247 ((2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid)

3D Structure for NP0165247 ((2r)-2-hydroxy-n-[(2s,3r,4e,13z)-3-hydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,13-dien-2-yl]tetradecanimidic acid)