NP-MRD: Showing NP-Card for (2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid (NP0268932)

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Record Information

Version

2.0

Created at

2022-09-08 14:12:54 UTC

Updated at

2022-09-08 14:12:54 UTC

NP-MRD ID

NP0268932

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid

Description

(2R,19Z)-N-[(1S,2S,3R,7Z)-1-[(beta-D-Glucopyranosyloxy)methyl]-2,3-dihydroxy-7-heptadecenyl]-2-hydroxy-19-octacosenamide 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,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid is found in Euphorbia characias. Based on a literature review very few articles have been published on (2R,19Z)-N-[(1S,2S,3R,7Z)-1-[(beta-D-Glucopyranosyloxy)methyl]-2,3-dihydroxy-7-heptadecenyl]-2-hydroxy-19-octacosenamide.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309082216122D          

 63 63  0  0  1  0            999 V2000
    2.1434  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    9.2881  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   21.4341   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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  5  6  1  0  0  0  0
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  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
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 62 63  1  0  0  0  0
M  END


  Mrv1652309082216122D          

 63 63  0  0  1  0            999 V2000
    2.1434  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.0013  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.5737  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   25.0065  -13.6125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210  -14.0250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   26.4354  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499  -14.0250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   26.4354  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065  -15.2625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   25.0065  -16.0875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920  -14.8500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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 62 63  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0268932

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCC\C=C/CCC[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)CCCCCCCCCCCCCCCC\C=C/CCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C52H99NO10/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-25-26-27-28-30-32-34-36-38-40-45(56)51(61)53-43(42-62-52-50(60)49(59)48(58)46(41-54)63-52)47(57)44(55)39-37-35-33-31-29-16-14-12-10-8-6-4-2/h17-18,31,33,43-50,52,54-60H,3-16,19-30,32,34-42H2,1-2H3,(H,53,61)/b18-17-,33-31-/t43-,44+,45+,46+,47-,48+,49-,50+,52+/m0/s1

> <INCHI_KEY>
ROFBFXSSLSYVGV-LTPLXAISSA-N

> <FORMULA>
C52H99NO10

> <MOLECULAR_WEIGHT>
898.361

> <EXACT_MASS>
897.726898392

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
162

> <JCHEM_AVERAGE_POLARIZABILITY>
113.28420798384981

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,19Z)-N-[(2S,3S,4R,8Z)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid

> <JCHEM_LOGP>
12.785148960666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.186219213757466

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.9516755134517494

> <JCHEM_PKA_STRONGEST_BASIC>
1.71479286425335

> <JCHEM_POLAR_SURFACE_AREA>
192.65999999999997

> <JCHEM_REFRACTIVITY>
258.047

> <JCHEM_ROTATABLE_BOND_COUNT>
44

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,19Z)-N-[(2S,3S,4R,8Z)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       4.001 -28.490   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335 -27.720   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668 -28.490   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002 -27.720   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336 -28.490   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669 -27.720   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.003 -28.490   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      13.337 -27.720   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      14.670 -28.490   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      16.004 -27.720   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      16.004 -26.180   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      17.338 -25.410   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      18.672 -26.180   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.005 -25.410   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      21.339 -26.180   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      22.673 -25.410   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      24.006 -26.180   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      25.340 -25.410   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      26.674 -26.180   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      28.007 -25.410   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      29.341 -26.180   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      30.675 -25.410   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      32.008 -26.180   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      33.342 -25.410   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      34.676 -26.180   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      36.009 -25.410   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      37.343 -26.180   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      37.343 -27.720   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      38.677 -25.410   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      38.677 -23.870   0.000  0.00  0.00           O+0
HETATM   31  N   UNK     0      40.010 -26.180   0.000  0.00  0.00           N+0
HETATM   32  C   UNK     0      41.344 -25.410   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      42.678 -26.180   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      44.011 -25.410   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      45.345 -26.180   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      46.679 -25.410   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      48.012 -26.180   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      49.346 -25.410   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      50.680 -26.180   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      48.012 -27.720   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      49.346 -28.490   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      46.679 -28.490   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      46.679 -30.030   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      45.345 -27.720   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      44.011 -28.490   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0      41.344 -23.870   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      40.010 -23.100   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      42.678 -23.100   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0      44.011 -23.870   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0      42.678 -21.560   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      44.011 -20.790   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      45.345 -21.560   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      46.679 -20.790   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      46.679 -19.250   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      45.345 -18.480   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      45.345 -16.940   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      44.011 -16.170   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      44.011 -14.630   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      42.678 -13.860   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0      42.678 -12.320   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0      41.344 -11.550   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0      41.344 -10.010   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0      40.010  -9.240   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                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33   46                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   44                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   40                                                  
CONECT   38   37   39                                                       
CONECT   39   38                                                            
CONECT   40   37   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   35   45                                                  
CONECT   45   44                                                            
CONECT   46   32   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49   50                                                  
CONECT   49   48                                                            
CONECT   50   48   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   61                                                       
CONECT   61   60   62                                                       
CONECT   62   61   63                                                       
CONECT   63   62                                                            
MASTER        0    0    0    0    0    0    0    0   63    0  126    0
END

View in JSmol

Synonyms

Value	Source
(2R,19Z)-N-[(1S,2S,3R,7Z)-1-[(b-D-Glucopyranosyloxy)methyl]-2,3-dihydroxy-7-heptadecenyl]-2-hydroxy-19-octacosenamide	Generator
(2R,19Z)-N-[(1S,2S,3R,7Z)-1-[(Β-D-glucopyranosyloxy)methyl]-2,3-dihydroxy-7-heptadecenyl]-2-hydroxy-19-octacosenamide	Generator

Chemical Formula

C₅₂H₉₉NO₁₀

Average Mass

898.3610 Da

Monoisotopic Mass

897.72690 Da

IUPAC Name

(2R,19Z)-N-[(2S,3S,4R,8Z)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid

Traditional Name

(2R,19Z)-N-[(2S,3S,4R,8Z)-3,4-dihydroxy-1-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCC\C=C/CCC[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)CCCCCCCCCCCCCCCC\C=C/CCCCCCCC

InChI Identifier

InChI=1S/C52H99NO10/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-25-26-27-28-30-32-34-36-38-40-45(56)51(61)53-43(42-62-52-50(60)49(59)48(58)46(41-54)63-52)47(57)44(55)39-37-35-33-31-29-16-14-12-10-8-6-4-2/h17-18,31,33,43-50,52,54-60H,3-16,19-30,32,34-42H2,1-2H3,(H,53,61)/b18-17-,33-31-/t43-,44+,45+,46+,47-,48+,49-,50+,52+/m0/s1

InChI Key

ROFBFXSSLSYVGV-LTPLXAISSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Euphorbia characias	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
Fatty acyl glycoside of mono- or disaccharide
Alkyl glycoside
Hexose monosaccharide
Glycosyl compound
O-glycosyl compound
Fatty amide
Fatty acyl
Monosaccharide
N-acyl-amine
Oxane
Carboxamide group
Secondary carboxylic acid amide
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Acetal
Carboxylic acid derivative
Polyol
Organonitrogen compound
Organopnictogen compound
Organic nitrogen compound
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Carbonyl group
Organic oxide
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	12.79	ChemAxon
pKa (Strongest Acidic)	3.95	ChemAxon
pKa (Strongest Basic)	1.71	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	192.66 Å²	ChemAxon
Rotatable Bond Count	44	ChemAxon
Refractivity	258.05 m³·mol⁻¹	ChemAxon
Polarizability	113.28 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

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

101942173

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid (NP0268932)

MOL for NP0268932 ((2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid)

3D MOL for NP0268932 ((2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid)

3D SDF for NP0268932 ((2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid)

3D-SDF for NP0268932 ((2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid)

PDB for NP0268932 ((2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid)

3D PDB for NP0268932 ((2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid)

SMILES for NP0268932 ((2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid)

INCHI for NP0268932 ((2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid)

Structure for NP0268932 ((2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid)

3D Structure for NP0268932 ((2r,19z)-n-[(2s,3s,4r,8z)-3,4-dihydroxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}octadec-8-en-2-yl]-2-hydroxyoctacos-19-enimidic acid)