NP-MRD: Showing NP-Card for (2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid (NP0240831)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 00:44:45 UTC

Updated at

2022-09-07 00:44:45 UTC

NP-MRD ID

NP0240831

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid

Description

(2R,3S,17Z)-N-[(2S,3S,4R)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid belongs to the class of organic compounds known as glycosphingolipids. These are sphingolipids containing a saccharide moiety glycosidically attached to the sphingoid base. Although saccharide moieties are mostly O-glycosidically linked to the ceramide moiety, other sphingolipids with glycosidic bonds of other types (e.G. S-,C-, or N-type) has been reported. (2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid is found in Catathelasma ventricosum. Based on a literature review very few articles have been published on (2R,3S,17Z)-N-[(2S,3S,4R)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072202442D          

 60 60  0  0  1  0            999 V2000
  -15.3213   -6.0756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.6588   -5.5839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.9018   -5.9117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2393   -5.4200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4823   -5.7478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8198   -5.2560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0627   -5.5839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4003   -5.0921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4949   -4.2726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8325   -3.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0754   -4.1087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4130   -3.6169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6559   -3.9448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9935   -3.4530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2364   -3.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5740   -3.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8169   -3.6169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1545   -3.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3974   -3.4530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7350   -2.9613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9779   -3.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3154   -2.7974    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4101   -1.9778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5584   -3.1252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4637   -3.9448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1041   -2.6335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0094   -1.8139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8611   -2.9613    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5236   -2.4696    0.0000 C   0  0  1  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
    0.6719   -1.3222    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5772   -0.5026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1798   -0.1748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2745    0.6448    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0315    0.9726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1262    1.7921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3880    1.1365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2933    1.9560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1450    0.8087    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8075    1.3004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2397   -0.0109    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9967   -0.3387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2806   -2.7974    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3753   -3.6169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9431   -2.3056    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8485   -1.4861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7002   -2.6335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3626   -2.1417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1197   -2.4696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7821   -1.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5392   -2.3056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2016   -1.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9587   -2.1417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6211   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3782   -1.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0406   -1.4861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7977   -1.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4601   -1.3222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2172   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8797   -1.1583    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  2  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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  4  0  0  0
 26 28  2  0  0  0  0
 29 28  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 32 31  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  1  1  0  0  0
 37 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 32 41  1  0  0  0  0
 41 42  1  1  0  0  0
 29 43  1  0  0  0  0
 43 44  1  1  0  0  0
 43 45  1  0  0  0  0
 45 46  1  6  0  0  0
 45 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
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
M  END

     RDKit          3D

153153  0  0  0  0  0  0  0  0999 V2000
   16.1747    1.1954    4.1360 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3338    1.0646    2.8766 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0668    1.6659    1.7169 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2588    1.5404    0.4726 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9171    2.2375    0.5210 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2738    1.9889   -0.8376 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9505    2.6139   -0.9830 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8699    1.9196   -1.2101 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8560    0.4634   -1.3395 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3737    0.0035   -2.7014 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3635   -1.4632   -2.7915 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5298   -2.3454   -1.9743 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0671   -2.2416   -2.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3982   -1.0177   -1.5892 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4892   -0.9583   -0.0837 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0170    0.2916    0.4929 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6666    0.8310    0.3545 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1233    1.2070   -0.9579 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7537    1.8627   -0.7872 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7978    0.9303   -0.1531 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4118    1.5515    0.0046 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7933    1.9912   -1.2589 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4332    2.6596   -1.0076 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5367    0.9608   -2.3129 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6744    0.2480   -2.5812 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6715    0.1280   -2.0336 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0819   -0.7073   -3.0566 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2510    0.2319   -0.8914 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4833   -0.6332   -0.6623 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2954   -1.0805    0.7408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1434   -1.9614    1.2942 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2246   -3.2076    0.7408 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5239   -3.3790    0.2861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7648   -4.5600   -0.3484 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9354   -5.2466    0.3429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2042   -6.4602   -0.2984 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6113   -5.5317   -0.3520 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.7510   -5.3288   -1.4430 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8859   -5.6041    0.9607 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3419   -6.6840    1.7510 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9771   -4.3189    1.7439 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7687   -4.1626    2.4150 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5659    0.3905   -0.8803 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5216    1.4554    0.0106 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9547   -0.0313   -1.1448 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.5316    1.1306   -1.8225 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7388   -0.0842    0.1559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2412   -0.2157   -0.1127 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6153   -1.4132   -0.8861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0726   -1.5631   -1.1264 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8227   -0.5959   -1.9211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9077    0.8253   -1.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4429    1.1420   -0.1923 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8291    0.6759    0.0814 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1720    1.0681    1.4981 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1199    2.5533    1.7398 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0828    3.3220    0.8736 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0174    4.8015    1.1283 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.3426    5.1781    2.5536 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.7110    4.7773    2.9984 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4234    2.2497    4.2917 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.0732    0.5465    3.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.5815    0.7574    4.9542 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.1721   -0.0224    2.7233 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3447    1.5400    3.0077 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.4090    2.7014    1.9164 H   0  0  0  0  0  0  0  0  0  0  0  0
   17.0040    1.0594    1.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.0737    0.4654    0.2673 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.8643    1.9007   -0.3969 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.2804    1.8917    1.3432 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.1148    3.3177    0.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3799    0.9612   -1.1613 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.9572    2.5714   -1.5506 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8774    3.7288   -0.8935 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.9069    2.4701   -1.3098 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0855    0.0989   -0.6137 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.7639   -0.0738   -1.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5165    0.5619   -3.0687 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1928    0.3204   -3.4760 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2973   -1.7649   -3.9022 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4574   -1.7826   -2.5709 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8160   -3.4058   -2.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8637   -2.2749   -0.8964 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7397   -2.4054   -3.1783 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5608   -3.1140   -1.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6828   -0.0568   -1.9956 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3036   -1.1880   -1.8723 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8528   -1.8497    0.2713 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5134   -1.2571    0.2331 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7420    1.1625    0.2370 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2364    0.2193    1.6251 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9536    0.0916    0.8326 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6185    1.7704    1.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8971    0.3663   -1.6642 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7927    1.9158   -1.5220 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9415    2.7360   -0.1106 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4105    2.2982   -1.7463 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6919   -0.0593   -0.6108 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1251    0.7413    0.9258 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5283    2.3618    0.7552 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8144    0.7590    0.5412 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4779    2.7549   -1.7615 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7893    2.9992   -1.8627 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2663    1.5743   -3.2434 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5583   -0.7116   -2.7223 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9147   -0.5833   -3.5989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4245   -1.3922   -1.4241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4083   -0.1247    1.3594 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2121   -1.3358    0.9655 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5558   -3.3328   -0.1537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0859   -4.4368   -1.4122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6944   -5.4926    1.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8520   -4.6293    0.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9507   -6.9100    0.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0637   -6.5480   -0.5209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2757   -5.6414   -2.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8141   -5.8617    0.7306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3842   -7.5118    1.2082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8435   -4.3544    2.4235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6639   -5.0150    2.9470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2389    0.9644   -1.8811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8034    2.3132   -0.3683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1265   -0.8497   -1.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6372    1.8452   -1.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4187   -0.8652    0.8494 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6172    0.8928    0.6630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6015    0.7506   -0.4213 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6666   -0.3672    0.9341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2997   -2.3562   -0.3291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0445   -1.5180   -1.8496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2662   -2.5867   -1.6206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5272   -1.7491   -0.1042 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8754   -0.9915   -2.0671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3706   -0.6174   -2.9719 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7634    1.2327   -2.2493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0714    1.4484   -1.9030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8123    0.8379    0.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4767    2.2729   -0.1424 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9668   -0.4130   -0.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5936    1.1814   -0.5790 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3428    0.6355    2.1330 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.1270    0.6212    1.8436 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4235    2.7053    2.8033 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0967    2.9367    1.6585 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.0936    2.9205    1.0810 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.8480    3.1583   -0.1836 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9814    5.1526    0.9438 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.6911    5.3142    0.4310 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5662    4.8443    3.2581 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.3087    6.3070    2.5869 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.7799    3.7246    3.3245 H   0  0  0  0  0  0  0  0  0  0  0  0
  -14.9763    5.3926    3.8942 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.4763    4.9934    2.2316 H   0  0  0  0  0  0  0  0  0  0  0  0
 60 59  1  0
 59 58  1  0
 58 57  1  0
 57 56  1  0
 56 55  1  0
 55 54  1  0
 54 53  1  0
 53 52  1  0
 52 51  1  0
 51 50  1  0
 50 49  1  0
 49 48  1  0
 48 47  1  0
 47 45  1  0
 45 46  1  0
 45 43  1  0
 43 44  1  0
 43 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 34 37  1  0
 37 38  1  0
 37 39  1  0
 39 40  1  0
 39 41  1  0
 41 42  1  0
 29 28  1  0
 28 26  2  0
 26 27  1  0
 26 24  1  0
 24 25  1  0
 24 22  1  0
 22 23  1  0
 22 21  1  0
 21 20  1  0
 20 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
 41 32  1  0
 60151  1  0
 60152  1  0
 60153  1  0
 59149  1  0
 59150  1  0
 58147  1  0
 58148  1  0
 57145  1  0
 57146  1  0
 56143  1  0
 56144  1  0
 55141  1  0
 55142  1  0
 54139  1  0
 54140  1  0
 53137  1  0
 53138  1  0
 52135  1  0
 52136  1  0
 51133  1  0
 51134  1  0
 50131  1  0
 50132  1  0
 49129  1  0
 49130  1  0
 48127  1  0
 48128  1  0
 47125  1  0
 47126  1  0
 45123  1  6
 46124  1  0
 43121  1  6
 44122  1  0
 29107  1  6
 30108  1  0
 30109  1  0
 32110  1  6
 34111  1  6
 35112  1  0
 35113  1  0
 36114  1  0
 37115  1  6
 38116  1  0
 39117  1  6
 40118  1  0
 41119  1  1
 42120  1  0
 27106  1  0
 24104  1  6
 25105  1  0
 22102  1  6
 23103  1  0
 21100  1  0
 21101  1  0
 20 98  1  0
 20 99  1  0
 19 96  1  0
 19 97  1  0
 18 94  1  0
 18 95  1  0
 17 92  1  0
 17 93  1  0
 16 90  1  0
 16 91  1  0
 15 88  1  0
 15 89  1  0
 14 86  1  0
 14 87  1  0
 13 84  1  0
 13 85  1  0
 12 82  1  0
 12 83  1  0
 11 80  1  0
 11 81  1  0
 10 78  1  0
 10 79  1  0
  9 76  1  0
  9 77  1  0
  8 75  1  0
  7 74  1  0
  6 72  1  0
  6 73  1  0
  5 70  1  0
  5 71  1  0
  4 68  1  0
  4 69  1  0
  3 66  1  0
  3 67  1  0
  2 64  1  0
  2 65  1  0
  1 61  1  0
  1 62  1  0
  1 63  1  0
M  END


  Mrv1652309072202442D          

 60 60  0  0  1  0            999 V2000
  -15.3213   -6.0756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.6588   -5.5839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.9018   -5.9117    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2393   -5.4200    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4823   -5.7478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.8198   -5.2560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0627   -5.5839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4003   -5.0921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4949   -4.2726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8325   -3.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0754   -4.1087    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4130   -3.6169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6559   -3.9448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9935   -3.4530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2364   -3.7808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5740   -3.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8169   -3.6169    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1545   -3.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3974   -3.4530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7350   -2.9613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9779   -3.2891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3154   -2.7974    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4101   -1.9778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5584   -3.1252    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4637   -3.9448    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1041   -2.6335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0094   -1.8139    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8611   -2.9613    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5236   -2.4696    0.0000 C   0  0  1  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
    0.6719   -1.3222    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5772   -0.5026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1798   -0.1748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2745    0.6448    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0315    0.9726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1262    1.7921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3880    1.1365    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2933    1.9560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1450    0.8087    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8075    1.3004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2397   -0.0109    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9967   -0.3387    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2806   -2.7974    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3753   -3.6169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9431   -2.3056    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8485   -1.4861    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7002   -2.6335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3626   -2.1417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1197   -2.4696    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7821   -1.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5392   -2.3056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2016   -1.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9587   -2.1417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6211   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3782   -1.9778    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0406   -1.4861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7977   -1.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4601   -1.3222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2172   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8797   -1.1583    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  2  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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  4  0  0  0
 26 28  2  0  0  0  0
 29 28  1  1  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 32 31  1  6  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  6  0  0  0
 35 36  1  0  0  0  0
 34 37  1  0  0  0  0
 37 38  1  1  0  0  0
 37 39  1  0  0  0  0
 39 40  1  6  0  0  0
 39 41  1  0  0  0  0
 32 41  1  0  0  0  0
 41 42  1  1  0  0  0
 29 43  1  0  0  0  0
 43 44  1  1  0  0  0
 43 45  1  0  0  0  0
 45 46  1  6  0  0  0
 45 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
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0240831

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCC[C@@H](O)[C@@H](O)[C@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)N=C(O)[C@H](O)[C@@H](O)CCCCCCCCCCCCC\C=C/CCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C48H93NO11/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-25-27-29-31-33-35-40(52)43(54)47(58)49-38(37-59-48-46(57)45(56)44(55)41(36-50)60-48)42(53)39(51)34-32-30-28-26-24-16-14-12-10-8-6-4-2/h13,15,38-46,48,50-57H,3-12,14,16-37H2,1-2H3,(H,49,58)/b15-13-/t38-,39+,40-,41+,42-,43+,44+,45-,46+,48+/m0/s1

> <INCHI_KEY>
IUDRSGVTSFBWPF-JEUDDPGJSA-N

> <FORMULA>
C48H93NO11

> <MOLECULAR_WEIGHT>
860.268

> <EXACT_MASS>
859.674862819

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
153

> <JCHEM_AVERAGE_POLARIZABILITY>
107.51732963226898

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(17Z)-N-[(2S,3S,4R)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid

> <JCHEM_LOGP>
10.293892350333337

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.165201582354536

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.578315814980759

> <JCHEM_PKA_STRONGEST_BASIC>
1.4875439621525626

> <JCHEM_POLAR_SURFACE_AREA>
212.88999999999996

> <JCHEM_REFRACTIVITY>
239.88790000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
41

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(17Z)-N-[(2S,3S,4R)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0     -28.600 -11.341   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -27.363 -10.423   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -25.950 -11.035   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -24.713 -10.117   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -23.300 -10.729   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -22.064  -9.811   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -20.650 -10.423   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -19.414  -9.505   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -19.591  -7.975   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -18.354  -7.058   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -16.941  -7.670   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -15.704  -6.752   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -14.291  -7.364   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0     -13.055  -6.446   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -11.641  -7.058   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0     -10.405  -6.140   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -8.992  -6.752   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -7.755  -5.834   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -6.342  -6.446   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -5.105  -5.528   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -3.692  -6.140   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.455  -5.222   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.632  -3.692   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -1.042  -5.834   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.866  -7.364   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.194  -4.916   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.018  -3.386   0.000  0.00  0.00           O+0
HETATM   28  N   UNK     0       1.607  -5.528   0.000  0.00  0.00           N+0
HETATM   29  C   UNK     0       2.844  -4.610   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.254  -2.468   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       1.078  -0.938   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -0.336  -0.326   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -0.512   1.204   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.926   1.815   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      -2.102   3.345   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       0.724   2.121   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       0.548   3.651   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0       2.137   1.510   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       3.374   2.427   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       2.314  -0.020   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       3.727  -0.632   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0       4.257  -5.222   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       4.434  -6.752   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       5.494  -4.304   0.000  0.00  0.00           C+0
HETATM   46  O   UNK     0       5.317  -2.774   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0       6.907  -4.916   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       8.144  -3.998   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       9.557  -4.610   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      10.793  -3.692   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      12.206  -4.304   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      13.443  -3.386   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      14.856  -3.998   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      16.093  -3.080   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      17.506  -3.692   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      18.743  -2.774   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      20.156  -3.386   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      21.392  -2.468   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      22.805  -3.080   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      24.042  -2.162   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                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   43                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33   41                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   37                                                  
CONECT   35   34   36                                                       
CONECT   36   35                                                            
CONECT   37   34   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   32   42                                                  
CONECT   42   41                                                            
CONECT   43   29   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   47                                                  
CONECT   46   45                                                            
CONECT   47   45   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   56                                                       
CONECT   56   55   57                                                       
CONECT   57   56   58                                                       
CONECT   58   57   59                                                       
CONECT   59   58   60                                                       
CONECT   60   59                                                            
MASTER        0    0    0    0    0    0    0    0   60    0  120    0
END

View in JSmol

Synonyms

Value	Source
(2R,3S,17Z)-N-[(2S,3S,4R)-3,4-Dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidate	Generator

Chemical Formula

C₄₈H₉₃NO₁₁

Average Mass

860.2680 Da

Monoisotopic Mass

859.67486 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCC[C@@H](O)[C@@H](O)[C@H](CO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)N=C(O)[C@H](O)[C@@H](O)CCCCCCCCCCCCC\C=C/CCCCCC

InChI Identifier

InChI=1S/C48H93NO11/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-25-27-29-31-33-35-40(52)43(54)47(58)49-38(37-59-48-46(57)45(56)44(55)41(36-50)60-48)42(53)39(51)34-32-30-28-26-24-16-14-12-10-8-6-4-2/h13,15,38-46,48,50-57H,3-12,14,16-37H2,1-2H3,(H,49,58)/b15-13-/t38-,39+,40-,41+,42-,43+,44+,45-,46+,48+/m0/s1

InChI Key

IUDRSGVTSFBWPF-JEUDDPGJSA-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
Catathelasma ventricosum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glycosphingolipids. These are sphingolipids containing a saccharide moiety glycosidically attached to the sphingoid base. Although saccharide moieties are mostly O-glycosidically linked to the ceramide moiety, other sphingolipids with glycosidic bonds of other types (e.G. S-,C-, or N-type) has been reported.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Sphingolipids

Sub Class

Glycosphingolipids

Direct Parent

Glycosphingolipids

Alternative Parents

Substituents

Glycosphingolipid
Fatty acyl glycoside of mono- or disaccharide
Fatty acyl glycoside
Hexose monosaccharide
Alkyl glycoside
O-glycosyl compound
Glycosyl compound
Fatty acyl
Oxane
Monosaccharide
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Polyol
Carboximidic acid derivative
Carboximidic acid
Acetal
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Organonitrogen compound
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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162959308

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid (NP0240831)

MOL for NP0240831 ((2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid)

3D MOL for NP0240831 ((2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid)

3D SDF for NP0240831 ((2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid)

3D-SDF for NP0240831 ((2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid)

PDB for NP0240831 ((2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid)

3D PDB for NP0240831 ((2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid)

SMILES for NP0240831 ((2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid)

INCHI for NP0240831 ((2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid)

Structure for NP0240831 ((2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid)

3D Structure for NP0240831 ((2r,3s,17z)-n-[(2s,3s,4r)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadecan-2-yl]-2,3-dihydroxytetracos-17-enimidic acid)