NP-MRD: Showing NP-Card for 2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid (NP0279864)

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Record Information

Version

2.0

Created at

2022-09-09 05:24:25 UTC

Updated at

2022-09-09 05:24:25 UTC

NP-MRD ID

NP0279864

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid

Description

Cerebroside D 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. 2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid is found in Albatrellus ellisii, Cortinarius humidicola and Lactarius volemus. 2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid was first documented in 2003 (PMID: 15620183). Based on a literature review a small amount of articles have been published on Cerebroside D (PMID: 28129885) (PMID: 22789836) (PMID: 21954554).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092207242D          

 53 53  0  0  1  0            999 V2000
  -12.1460   -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
  -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 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 N   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  2  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  2  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
    0.7145    1.2375    0.0000 C   0  0  1  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  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   -0.0000    0.0000 C   0  0  1  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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    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
    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
    6.4302   -3.7125    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  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 21 22  1  4  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  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  2  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  2  0  0  0  0
 43 44  1  0  0  0  0
 43 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
 52 53  1  0  0  0  0
M  END

     RDKit          3D

134134  0  0  0  0  0  0  0  0999 V2000
    4.1888    2.7422    2.4381 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6606    2.8829    2.7237 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3541    3.7856    1.7526 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2756    3.3287    0.3127 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9097    1.9849    0.1987 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9158    1.4064   -1.1847 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5514    1.2208   -1.7594 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6921    0.2919   -0.9320 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2454   -1.0838   -0.7906 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2453   -1.8534    0.0873 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7161   -3.2696    0.3050 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8611   -4.0900   -0.9009 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7492   -4.3536   -1.8161 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5272   -5.0559   -1.3600 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6605   -4.3976   -0.3599 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4873   -5.2053    0.0817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5031   -5.6477   -0.9075 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0174   -6.4602   -1.9335 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4741   -4.7031   -1.4146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4233   -5.1902   -2.3331 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5304   -3.4780   -1.0931 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5786   -2.6098   -1.6818 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9128   -1.4084   -2.2473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2411   -0.6076   -1.3235 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6716    0.4607   -2.0192 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6304    0.6203   -1.7226 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2330    1.7471   -2.2127 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7738    2.6289   -1.1251 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3637    3.7327   -1.7447 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3747    2.5208   -3.1826 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3755    1.9281   -4.4436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0228    2.7679   -2.7033 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2525    4.0830   -2.3124 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4227    1.7618   -1.6498 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8055    1.5309   -1.8119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5506   -2.3442   -0.5699 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.0540   -3.5682   -0.0577 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7193   -1.4943   -0.9661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1676   -1.3246   -2.1688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3046   -0.4977   -2.5440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0478    0.2668   -1.5447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4244    1.3629   -0.8204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9631    2.5869   -0.8934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1951    2.7636   -1.7294 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3572    3.7028   -0.1659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1325    3.2751    0.6054 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5445    4.4551    1.3429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3063    4.0844    2.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6081    3.0282    3.1244 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3508    2.6690    3.9102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6169    1.6194    4.9544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6369    2.0556    5.9655 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2535    3.2842    6.7287 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9372    1.7159    2.1723 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9500    3.3969    1.5773 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5667    3.0617    3.3107 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1143    1.8743    2.7385 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8073    3.3536    3.7418 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8832    4.7942    1.8189 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4262    3.9102    1.9970 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8059    4.0667   -0.3006 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2144    3.3499   -0.0080 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9224    2.0523    0.6414 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3726    1.2242    0.8369 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5384    0.4941   -1.2632 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4392    2.1672   -1.8368 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6302    0.7614   -2.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0619    2.2005   -1.9058 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6683    0.1989   -1.3547 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5519    0.7564    0.0684 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2120   -1.1614   -0.2851 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2880   -1.5509   -1.8094 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2531   -1.3439    1.0714 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2351   -1.7724   -0.3188 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8098   -3.1076    0.6741 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2388   -3.6890    1.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2791   -5.0943   -0.5589 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7322   -3.6443   -1.4962 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3966   -3.4180   -2.3544 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1972   -4.9560   -2.6875 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9395   -5.3537   -2.2959 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8656   -6.0626   -0.9479 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3405   -3.3674   -0.7211 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2354   -4.1763    0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9123   -6.1312    0.5802 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0130   -4.6379    0.9246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1547   -6.4308   -0.3311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6354   -7.0884   -2.2834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2784   -6.0274   -2.8571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0263   -3.1814   -2.5145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1089   -1.6928   -2.9954 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5779   -0.7383   -2.8292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8164    0.3457   -3.1275 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1254    1.4045   -2.8149 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9781    2.9456   -0.4110 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5496    2.1539   -0.5137 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9293    4.5709   -1.4896 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8538    3.5266   -3.3072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3927    2.2796   -4.9776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7158    2.5976   -3.5818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0554    4.4723   -2.7303 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.0052    1.6328   -2.7637 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309092207242D          

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M  END
> <DATABASE_ID>
NP0279864

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCC(O)C(O)=NC(CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(O)\C=C\CC\C=C(/C)CCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C43H81NO9/c1-4-6-8-10-12-13-14-15-16-17-18-20-22-26-31-37(47)42(51)44-35(33-52-43-41(50)40(49)39(48)38(32-45)53-43)36(46)30-27-23-25-29-34(3)28-24-21-19-11-9-7-5-2/h27,29-30,35-41,43,45-50H,4-26,28,31-33H2,1-3H3,(H,44,51)/b30-27+,34-29+/t35?,36?,37?,38-,39-,40+,41-,43-/m1/s1

> <INCHI_KEY>
RIZIAUKTHDLMQX-PFFLVVKUSA-N

> <FORMULA>
C43H81NO9

> <MOLECULAR_WEIGHT>
756.119

> <EXACT_MASS>
755.591133192

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
134

> <JCHEM_AVERAGE_POLARIZABILITY>
94.23557290938443

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-hydroxy-N-[(4E,8E)-3-hydroxy-9-methyl-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid

> <JCHEM_LOGP>
9.813634649333336

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.203428504249672

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.983351048828699

> <JCHEM_PKA_STRONGEST_BASIC>
1.744799360136907

> <JCHEM_POLAR_SURFACE_AREA>
172.42999999999998

> <JCHEM_REFRACTIVITY>
214.80350000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
34

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
2-hydroxy-N-[(4E,8E)-3-hydroxy-9-methyl-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0     -22.673  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -21.339  -4.620   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -20.005  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -18.672  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -17.338  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -16.004  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -14.670  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -13.337  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   21  N   UNK     0       1.334  -5.390   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       0.000  -0.000   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.334   3.850   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      17.338  -5.390   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      20.005  -5.390   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      21.339  -4.620   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      22.673  -5.390   0.000  0.00  0.00           C+0
HETATM   53  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                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   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   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   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   53                                                       
CONECT   53   52                                                            
MASTER        0    0    0    0    0    0    0    0   53    0  106    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₃H₈₁NO₉

Average Mass

756.1190 Da

Monoisotopic Mass

755.59113 Da

IUPAC Name

2-hydroxy-N-[(4E,8E)-3-hydroxy-9-methyl-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid

Traditional Name

2-hydroxy-N-[(4E,8E)-3-hydroxy-9-methyl-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCC(O)C(O)=NC(CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)C(O)\C=C\CC\C=C(/C)CCCCCCCCC

InChI Identifier

InChI=1S/C43H81NO9/c1-4-6-8-10-12-13-14-15-16-17-18-20-22-26-31-37(47)42(51)44-35(33-52-43-41(50)40(49)39(48)38(32-45)53-43)36(46)30-27-23-25-29-34(3)28-24-21-19-11-9-7-5-2/h27,29-30,35-41,43,45-50H,4-26,28,31-33H2,1-3H3,(H,44,51)/b30-27+,34-29+/t35?,36?,37?,38-,39-,40+,41-,43-/m1/s1

InChI Key

RIZIAUKTHDLMQX-PFFLVVKUSA-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
Albatrellus ellisii	LOTUS Database	35616633
Cortinarius humidicola	LOTUS Database	35616633
Lactarius volemus	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	9.81	ChemAxon
pKa (Strongest Acidic)	3.98	ChemAxon
pKa (Strongest Basic)	1.74	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	172.43 Å²	ChemAxon
Rotatable Bond Count	34	ChemAxon
Refractivity	214.8 m³·mol⁻¹	ChemAxon
Polarizability	94.24 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

C00044623

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

100916010

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Lee SR, Lee D, Lee HJ, Noh HJ, Jung K, Kang KS, Kim KH: Renoprotective chemical constituents from an edible mushroom, Pleurotus cornucopiae in cisplatin-induced nephrotoxicity. Bioorg Chem. 2017 Apr;71:67-73. doi: 10.1016/j.bioorg.2017.01.012. Epub 2017 Jan 19. [PubMed:28129885 ]
Wu XF, Wu XX, Guo WJ, Luo Q, Gu YH, Shen Y, Tan RX, Sun Y, Xu Q: Cerebroside D, a glycoceramide compound, improves experimental colitis in mice with multiple targets against activated T lymphocytes. Toxicol Appl Pharmacol. 2012 Sep 15;263(3):296-302. doi: 10.1016/j.taap.2012.07.001. Epub 2012 Jul 10. [PubMed:22789836 ]
Zhang YG, Yuan WP, Xia XK, Jia AR, Liu X, Zhang MS, Liu CH: [The study of the secondary metabolites from fungus Paecilomyces sp]. Zhong Yao Cai. 2011 May;34(5):707-9. [PubMed:21954554 ]
Gao JM, Zhang AL, Yao HY, Shen J: [A study on the chemical constituents from Polyporus ellissi]. Zhongguo Zhong Yao Za Zhi. 2003 Oct;28(10):943-6. [PubMed:15620183 ]
LOTUS database [Link]

Showing NP-Card for 2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid (NP0279864)

MOL for NP0279864 (2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid)

3D MOL for NP0279864 (2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid)

3D SDF for NP0279864 (2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid)

3D-SDF for NP0279864 (2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid)

PDB for NP0279864 (2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid)

3D PDB for NP0279864 (2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid)

SMILES for NP0279864 (2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid)

INCHI for NP0279864 (2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid)

Structure for NP0279864 (2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid)

3D Structure for NP0279864 (2-hydroxy-n-[(4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadeca-4,8-dien-2-yl]octadecanimidic acid)