NP-MRD: Showing NP-Card for (2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid (NP0214711)

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Record Information

Version

2.0

Created at

2022-09-05 14:05:33 UTC

Updated at

2022-09-05 14:05:33 UTC

NP-MRD ID

NP0214711

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

Asperiamide C 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. Based on a literature review very few articles have been published on Asperiamide C.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052216052D          

 55 55  0  0  1  0            999 V2000
   -5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    3.3000    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    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    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
   -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  1  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  2  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
   13.5749   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -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  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 19 20  1  4  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 22  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  6  0  0  0
 30 32  1  0  0  0  0
 23 32  1  0  0  0  0
 32 33  1  1  0  0  0
 20 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  2  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  2  0  0  0  0
 41 42  1  0  0  0  0
 41 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
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
M  END

     RDKit          3D

138138  0  0  0  0  0  0  0  0999 V2000
  -13.2756    1.0808    4.7371 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.9349    1.0361    3.3930 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2615   -0.0790    2.5830 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.8701   -0.1861    1.2087 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2340   -1.1955    0.3598 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9555   -0.9756   -0.2899 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7338   -0.4611    0.3258 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6913    1.0101    0.5651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4277    1.4441    1.2726 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1731    1.1003    0.5538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1193    1.7297   -0.7915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8365    1.4042   -1.5364 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6758    1.9017   -0.7611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7357    1.0757   -0.3385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5413    1.4747    0.4405 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8670    2.6189    1.1809 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1285    0.3645    1.3038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0510    0.0115    2.3155 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0673   -0.3162    1.2683 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9494   -0.2174    0.3813 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6467   -1.5526   -0.2866 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7337   -1.9847   -1.0378 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5137   -3.2107   -1.6423 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5403   -3.0239   -3.0192 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8114   -2.8137   -3.5141 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7373   -1.5161   -4.3320 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3394   -0.4921   -3.4721 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8441   -2.6158   -2.4539 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0999   -2.6299   -3.1181 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9028   -3.7726   -1.4893 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6410   -3.3826   -0.3683 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5073   -4.1858   -1.1208 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2364   -5.4584   -1.6280 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3144    0.2511    1.0588 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1811    1.5162    1.6303 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4773    0.2078    0.0829 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3743    0.6974   -1.1226 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3698    0.7429   -2.1766 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7377    0.2435   -1.9206 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4893    0.9942   -0.9223 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5678    1.6816   -1.3556 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9428    1.6728   -2.7826 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3507    2.4476   -0.3788 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7983    1.9120   -0.4167 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6536    2.6522    0.5557 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0892    2.1160    0.4884 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6243    2.3394   -0.8529 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9940    2.0260   -1.2376 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5868    0.7002   -1.2010 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7282    0.0259    0.1327 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5807    0.8571    1.0820 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7414    0.2127    2.4329 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3997   -1.1215    2.3368 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5396   -1.6863    3.7411 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2134   -3.0522    3.6942 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4855    0.2970    4.8315 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.9610    0.9230    5.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7398    2.0430    4.9174 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.7536    2.0204    2.8940 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.0171    0.8331    3.5248 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2014    0.0348    2.6273 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.5437   -1.0298    3.1683 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.8382    0.8505    0.7311 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.9795   -0.3618    1.3151 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.9923   -1.4215   -0.4815 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1725   -2.1929    0.9499 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2118   -0.2756   -1.2046 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6702   -1.9123   -0.9187 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5534   -1.0319    1.2950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8148   -0.6948   -0.2915 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6746    1.5131   -0.4651 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5480    1.4356    1.0589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5205    2.5652    1.3759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4648    1.0406    2.3110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0808   -0.0160    0.5132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3249    1.4365    1.2163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1614    2.8315   -0.6880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9669    1.3220   -1.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7858    0.2946   -1.6025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9026    1.8313   -2.5423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5729    2.9584   -0.5217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8644    0.0188   -0.5914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7725    1.8031   -0.2893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9441    3.4125    0.6269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8264   -0.5696    1.9982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2224    0.5479   -0.3817 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2598   -1.4859   -0.8866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4762   -2.2797    0.5164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4792   -3.5503   -1.3386 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0574   -3.6164   -4.2262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9866   -1.6283   -5.1432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7338   -1.2393   -4.7302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9112    0.3166   -3.6000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7956   -1.6257   -1.9766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0676   -3.2867   -3.8819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4548   -4.6355   -1.9438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5977   -3.5803   -0.5129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4176   -4.2008    0.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7134   -5.4059   -2.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5654   -0.4601    1.8728 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7699    2.1968    1.2128 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4068   -0.2497    0.3763 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3826    1.1451   -1.3699 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9713    0.1005   -3.0399 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309052216052D          

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M  END
> <DATABASE_ID>
NP0214711

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCC\C(C)=C\CC\C=C\[C@@H](O)C(CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)N=C(O)[C@H](O)\C=C\CCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C45H83NO9/c1-4-6-8-10-12-14-16-18-20-22-24-28-33-39(49)44(53)46-37(35-54-45-43(52)42(51)41(50)40(34-47)55-45)38(48)32-29-25-27-31-36(3)30-26-23-21-19-17-15-13-11-9-7-5-2/h28-29,31-33,37-43,45,47-52H,4-27,30,34-35H2,1-3H3,(H,46,53)/b32-29+,33-28+,36-31+/t37?,38-,39-,40-,41-,42+,43-,45-/m1/s1

> <INCHI_KEY>
FLCIOTVHCJKHJR-LWZWQNNYSA-N

> <FORMULA>
C45H83NO9

> <MOLECULAR_WEIGHT>
782.157

> <EXACT_MASS>
781.606783257

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
138

> <JCHEM_AVERAGE_POLARIZABILITY>
97.69742100379383

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <JCHEM_LOGP>
10.49675778266667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.19989163817087

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.70226240386384

> <JCHEM_PKA_STRONGEST_BASIC>
1.5585268417348062

> <JCHEM_POLAR_SURFACE_AREA>
172.42999999999998

> <JCHEM_REFRACTIVITY>
224.96810000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
35

> <JCHEM_RULE_OF_FIVE>
0

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0     -10.669  10.780   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -10.669   9.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.336   8.470   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.336   6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.002   6.160   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.002   4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.668   3.850   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.335   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667  -3.080   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  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0       1.334  -5.390   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.334   3.850   0.000  0.00  0.00           O+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       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      13.337  -4.620   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      14.670  -5.390   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      16.004  -4.620   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      17.338  -5.390   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      18.672  -4.620   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      20.005  -5.390   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      21.339  -4.620   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      22.673  -5.390   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      24.006  -4.620   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      25.340  -5.390   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      26.674  -4.620   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      28.007  -5.390   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      29.341  -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   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   34                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   32                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   23   33                                                  
CONECT   33   32                                                            
CONECT   34   20   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   43                                                  
CONECT   42   41                                                            
CONECT   43   41   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   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54                                                            
MASTER        0    0    0    0    0    0    0    0   55    0  110    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₅H₈₃NO₉

Average Mass

782.1570 Da

Monoisotopic Mass

781.60678 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCC\C(C)=C\CC\C=C\[C@@H](O)C(CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)N=C(O)[C@H](O)\C=C\CCCCCCCCCCCC

InChI Identifier

InChI=1S/C45H83NO9/c1-4-6-8-10-12-14-16-18-20-22-24-28-33-39(49)44(53)46-37(35-54-45-43(52)42(51)41(50)40(34-47)55-45)38(48)32-29-25-27-31-36(3)30-26-23-21-19-17-15-13-11-9-7-5-2/h28-29,31-33,37-43,45,47-52H,4-27,30,34-35H2,1-3H3,(H,46,53)/b32-29+,33-28+,36-31+/t37?,38-,39-,40-,41-,42+,43-,45-/m1/s1

InChI Key

FLCIOTVHCJKHJR-LWZWQNNYSA-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 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
Monosaccharide
N-acyl-amine
Oxane
Fatty acyl
Secondary carboxylic acid amide
Secondary alcohol
Carboxamide group
Organoheterocyclic compound
Polyol
Oxacycle
Carboxylic acid derivative
Acetal
Organic nitrogen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Alcohol
Organonitrogen compound
Carbonyl group
Organooxygen compound
Primary alcohol
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	10.5	ChemAxon
pKa (Strongest Acidic)	3.7	ChemAxon
pKa (Strongest Basic)	1.56	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	35	ChemAxon
Refractivity	224.97 m³·mol⁻¹	ChemAxon
Polarizability	97.7 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

C00048619

Chemspider ID

78440825

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584034

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid (NP0214711)

MOL for NP0214711 ((2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid)

3D MOL for NP0214711 ((2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid)

3D SDF for NP0214711 ((2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid)

3D-SDF for NP0214711 ((2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid)

PDB for NP0214711 ((2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid)

3D PDB for NP0214711 ((2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid)

SMILES for NP0214711 ((2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid)

INCHI for NP0214711 ((2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid)

Structure for NP0214711 ((2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid)

3D Structure for NP0214711 ((2r,3e)-2-hydroxy-n-[(3r,4e,8e)-3-hydroxy-9-methyl-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}docosa-4,8-dien-2-yl]hexadec-3-enimidic acid)