NP-MRD: Showing NP-Card for (2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid (NP0157716)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 15:09:55 UTC

Updated at

2022-09-02 15:09:55 UTC

NP-MRD ID

NP0157716

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid

Description

Symbioramide belongs to the class of organic compounds known as long-chain ceramides. These are ceramides bearing a long chain fatty acid. (2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid was first documented in 2003 (PMID: 12704863). Based on a literature review very few articles have been published on Symbioramide (PMID: 12662053).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022217092D          

 41 40  0  0  1  0            999 V2000
    1.0990   11.9906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937   11.1711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9507   10.8433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0454   10.0237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8025    9.6959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8971    8.8763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542    8.5485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7488    7.7290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5059    7.4011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6005    6.5816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3576    6.2538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4522    5.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2093    5.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3039    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0610    3.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1556    3.1394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9127    2.8116    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0073    1.9921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5751    3.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4805    4.1229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3322    2.9755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9946    3.4673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9000    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5624    4.7786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7517    3.1394    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.8463    2.3199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4141    3.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1712    3.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8337    3.7951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5907    3.4673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2532    3.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0102    3.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6727    4.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4297    3.7951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0922    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8493    3.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5117    4.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2688    4.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9312    4.6146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6883    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3507    4.7786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  4  0  0  0
 19 21  2  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
M  END

     RDKit          3D

112111  0  0  0  0  0  0  0  0999 V2000
  -11.9780    1.9514   -0.2433 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9262    2.3455   -1.2403 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4450    1.1308   -2.0188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8828    0.1730   -0.9471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3674   -1.0691   -1.5955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7943   -2.0910   -0.6781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6450   -2.7702    0.2954 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3866   -2.0428    1.3354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6050   -1.1952    2.2814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6112   -1.9668    3.0950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8647   -1.0921    4.0650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0902   -0.0247    3.3833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0599   -0.6743    2.4560 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3101    0.4384    1.7891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2685   -0.0226    0.8420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0053    0.2861    1.0047 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9431   -0.1924    0.0252 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6387   -0.2964   -1.1937 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9552    0.8921   -0.0367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4238    2.2073   -0.1794 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2863    0.6893    0.0318 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9642   -0.5514    0.1742 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9418   -1.3984   -1.0683 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6431   -2.5879   -0.8365 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4102   -0.2721    0.5355 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4791    0.4531    1.7408 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0631    0.5027   -0.5788 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5221    0.7420   -0.1966 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2701    1.5142   -1.2627 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3100    0.8168   -2.5953 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0940    1.4840   -3.6289 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5157    1.5337   -3.7932 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6295    1.8395   -2.9365 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1776    0.9146   -1.9226 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4441    0.4177   -0.7756 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2458   -0.5769    0.0705 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5371    0.0418    0.6001 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2024   -1.0202    1.4161 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4664   -0.7214    2.0986 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5952   -0.3460    1.2091 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4205    0.9207    0.4413 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7208    2.7831   -0.0855 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5038    1.7602    0.7651 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5467    1.0594   -0.5434 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3275    3.0905   -1.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0357    2.7497   -0.7015 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6646    1.3992   -2.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2976    0.5988   -2.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6717    0.0144   -0.2249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0088    0.7045   -0.4818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5943   -0.7197   -2.3497 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1526   -1.5300   -2.2696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4048   -2.9167   -1.3815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8158   -1.7240   -0.2395 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0552   -3.6442    0.7198 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4430   -3.3324   -0.3111 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3379   -1.6387    1.0039 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7614   -2.9117    2.0446 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3513   -0.7662    3.0122 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1243   -0.3272    1.8171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9303   -2.5754    2.4446 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1287   -2.7427    3.7371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6352   -0.6334    4.7317 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1555   -1.6965    4.6685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5583    0.6062    4.1493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6755    0.6916    2.7916 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5372   -1.2971    1.6952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3180   -1.2568    3.0731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8340    1.0318    2.6200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9606    1.1413    1.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5452   -0.6267   -0.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7040    0.8849    1.8394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5966   -1.1449    0.4190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5704   -1.2610   -1.4502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1734    2.9531    0.4595 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5519   -1.1896    0.9941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1029   -1.6904   -1.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3579   -0.9298   -1.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0086   -2.9587   -1.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9133   -1.2403    0.6994 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1663    1.3716    1.5448 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5213    1.4599   -0.6848 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1000   -0.0815   -1.5178 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0494   -0.2028   -0.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4994    1.3980    0.7090 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5865    2.4456   -1.5142 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1866    1.9118   -0.8726 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5954   -0.2634   -2.4792 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2235    0.7499   -2.9303 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6750    1.0893   -4.6633 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6884    2.5855   -3.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6469    2.2086   -4.7832 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8253    0.5277   -4.3633 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5115    2.9010   -2.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5258    2.0930   -3.6376 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1819    1.3570   -1.5525 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.6114    0.0315   -2.5444 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1200    1.2342   -0.0520 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5343   -0.1300   -1.0565 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4925   -1.4785   -0.4812 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6201   -0.8256    0.9481 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3631    0.9447    1.1688 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1669    0.1603   -0.3247 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4265   -1.3682    2.1691 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.3411   -1.8997    0.6946 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3430    0.0286    2.9386 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.7900   -1.6554    2.6455 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.6954   -1.2097    0.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.5843   -0.3525    1.7680 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3540    1.5727    0.5529 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6161    1.5310    0.8489 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3527    0.7358   -0.6396 H   0  0  0  0  0  0  0  0  0  0  0  0
 41 40  1  0
 40 39  1  0
 39 38  1  0
 38 37  1  0
 37 36  1  0
 36 35  1  0
 35 34  1  0
 34 33  1  0
 33 32  1  0
 32 31  1  0
 31 30  1  0
 30 29  1  0
 29 28  1  0
 28 27  1  0
 27 25  1  0
 25 26  1  0
 25 22  1  0
 22 23  1  0
 23 24  1  0
 22 21  1  0
 21 19  2  0
 19 20  1  0
 19 17  1  0
 17 18  1  0
 17 16  1  0
 16 15  2  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  1  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
 41110  1  0
 41111  1  0
 41112  1  0
 40108  1  0
 40109  1  0
 39106  1  0
 39107  1  0
 38104  1  0
 38105  1  0
 37102  1  0
 37103  1  0
 36100  1  0
 36101  1  0
 35 98  1  0
 35 99  1  0
 34 96  1  0
 34 97  1  0
 33 94  1  0
 33 95  1  0
 32 92  1  0
 32 93  1  0
 31 90  1  0
 31 91  1  0
 30 88  1  0
 30 89  1  0
 29 86  1  0
 29 87  1  0
 28 84  1  0
 28 85  1  0
 27 82  1  0
 27 83  1  0
 25 80  1  1
 26 81  1  0
 22 76  1  1
 23 77  1  0
 23 78  1  0
 24 79  1  0
 20 75  1  0
 17 73  1  1
 18 74  1  0
 16 72  1  0
 15 71  1  0
 14 69  1  0
 14 70  1  0
 13 67  1  0
 13 68  1  0
 12 65  1  0
 12 66  1  0
 11 63  1  0
 11 64  1  0
 10 61  1  0
 10 62  1  0
  9 59  1  0
  9 60  1  0
  8 57  1  0
  8 58  1  0
  7 55  1  0
  7 56  1  0
  6 53  1  0
  6 54  1  0
  5 51  1  0
  5 52  1  0
  4 49  1  0
  4 50  1  0
  3 47  1  0
  3 48  1  0
  2 45  1  0
  2 46  1  0
  1 42  1  0
  1 43  1  0
  1 44  1  0
M  END


  Mrv1652309022217092D          

 41 40  0  0  1  0            999 V2000
    1.0990   11.9906    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1937   11.1711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9507   10.8433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0454   10.0237    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8025    9.6959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8971    8.8763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6542    8.5485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7488    7.7290    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5059    7.4011    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6005    6.5816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3576    6.2538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4522    5.4342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2093    5.1064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3039    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0610    3.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1556    3.1394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9127    2.8116    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.0073    1.9921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5751    3.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4805    4.1229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.3322    2.9755    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.9946    3.4673    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.9000    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5624    4.7786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.7517    3.1394    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.8463    2.3199    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.4141    3.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1712    3.3034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8337    3.7951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5907    3.4673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2532    3.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0102    3.6312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6727    4.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4297    3.7951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0922    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8493    3.9590    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5117    4.4507    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2688    4.1229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9312    4.6146    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6883    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3507    4.7786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  4  0  0  0
 19 21  2  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0157716

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)N=C(O)[C@H](O)\C=C\CCCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C36H71NO4/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-35(40)36(41)37-33(32-38)34(39)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h29,31,33-35,38-40H,3-28,30,32H2,1-2H3,(H,37,41)/b31-29+/t33-,34+,35+/m0/s1

> <INCHI_KEY>
LJKCPJOLKILGIR-FNQQTZKRSA-N

> <FORMULA>
C36H71NO4

> <MOLECULAR_WEIGHT>
581.967

> <EXACT_MASS>
581.53830977

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
77.64246830049495

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3E)-N-[(2S,3R)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid

> <ALOGPS_LOGP>
9.29

> <JCHEM_LOGP>
11.703030680000001

> <ALOGPS_LOGS>
-6.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.88870872183136

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.051162126293947

> <JCHEM_PKA_STRONGEST_BASIC>
1.9688916277520772

> <JCHEM_POLAR_SURFACE_AREA>
93.28

> <JCHEM_REFRACTIVITY>
176.9916

> <JCHEM_ROTATABLE_BOND_COUNT>
32

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.11e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3E)-N-[(2S,3R)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       2.052  22.383   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.228  20.853   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.641  20.241   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.818  18.711   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.231  18.099   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.408  16.569   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.821  15.957   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.998  14.427   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.411  13.815   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.588  12.286   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.001  11.674   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.177  10.144   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      11.591   9.532   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.767   8.002   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.180   7.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.357   5.860   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.770   5.248   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      14.947   3.719   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      16.007   6.166   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      15.830   7.696   0.000  0.00  0.00           O+0
HETATM   21  N   UNK     0      17.420   5.554   0.000  0.00  0.00           N+0
HETATM   22  C   UNK     0      18.657   6.472   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      18.480   8.002   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      19.717   8.920   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      20.070   5.860   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      20.247   4.330   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      21.306   6.778   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      22.720   6.166   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      23.956   7.084   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      25.369   6.472   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      26.606   7.390   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      28.019   6.778   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      29.256   7.696   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      30.669   7.084   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      31.905   8.002   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      33.319   7.390   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      34.555   8.308   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      35.968   7.696   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      37.205   8.614   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      38.618   8.002   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      39.855   8.920   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   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₆H₇₁NO₄

Average Mass

581.9670 Da

Monoisotopic Mass

581.53831 Da

IUPAC Name

(2R,3E)-N-[(2S,3R)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid

Traditional Name

(2R,3E)-N-[(2S,3R)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)N=C(O)[C@H](O)\C=C\CCCCCCCCCCCCCC

InChI Identifier

InChI=1S/C36H71NO4/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-35(40)36(41)37-33(32-38)34(39)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h29,31,33-35,38-40H,3-28,30,32H2,1-2H3,(H,37,41)/b31-29+/t33-,34+,35+/m0/s1

InChI Key

LJKCPJOLKILGIR-FNQQTZKRSA-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 long-chain ceramides. These are ceramides bearing a long chain fatty acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Sphingolipids

Sub Class

Ceramides

Direct Parent

Long-chain ceramides

Alternative Parents

Substituents

Long-chain ceramide
N-acyl-amine
Carboxamide group
Secondary carboxylic acid amide
Secondary alcohol
Carboxylic acid derivative
Alcohol
Primary alcohol
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	9.29	ALOGPS
logP	11.7	ChemAxon
logS	-6.7	ALOGPS
pKa (Strongest Acidic)	4.05	ChemAxon
pKa (Strongest Basic)	1.97	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	93.28 Å²	ChemAxon
Rotatable Bond Count	32	ChemAxon
Refractivity	176.99 m³·mol⁻¹	ChemAxon
Polarizability	77.64 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

4947893

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6443941

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Nakagawa M: [Synthetic study of biologically important nitrogen containing natural products: development of new methodology and design of leading compounds for new pharmaceuticals]. Yakugaku Zasshi. 2003 Apr;123(4):225-48. doi: 10.1248/yakushi.123.225. [PubMed:12704863 ]
Azuma H, Takao R, Niiro H, Shikata K, Tamagaki S, Tachibana T, Ogino K: Total syntheses of symbioramide derivatives from l-serine and their antileukemic activities. J Org Chem. 2003 Apr 4;68(7):2790-7. doi: 10.1021/jo0206824. [PubMed:12662053 ]
LOTUS database [Link]

Showing NP-Card for (2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid (NP0157716)

MOL for NP0157716 ((2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid)

3D MOL for NP0157716 ((2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid)

3D SDF for NP0157716 ((2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid)

3D-SDF for NP0157716 ((2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid)

PDB for NP0157716 ((2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid)

3D PDB for NP0157716 ((2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid)

SMILES for NP0157716 ((2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid)

INCHI for NP0157716 ((2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid)

Structure for NP0157716 ((2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid)

3D Structure for NP0157716 ((2r,3e)-n-[(2s,3r)-1,3-dihydroxyoctadecan-2-yl]-2-hydroxyoctadec-3-enimidic acid)