NP-MRD: Showing NP-Card for Psychosine sulfate (NP0339167)

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Record Information

Version

2.0

Created at

2024-09-11 20:01:46 UTC

Updated at

2024-09-11 20:01:47 UTC

NP-MRD ID

NP0339167

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Psychosine sulfate

Description

Psychosine sulfate 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. Psychosine sulfate is a very strong basic compound (based on its pKa). Psychosine sulfate is a potentially toxic compound.

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 02251208152D          

 36 36  0  0  1  0            999 V2000
   15.6998  -19.0497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -18.3353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -17.6208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -16.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -16.1918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -15.4773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -14.7629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -14.0484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -13.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -12.6194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -11.9049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -11.1905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -10.4760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873   -9.7615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998   -9.0470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873   -8.3326    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.6998   -7.6181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.4623   -8.3326    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.0498   -7.6181    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.0498   -9.0470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2248   -9.0470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8123   -9.7615    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.2248  -10.4760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8123  -11.1905    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.2248  -11.9049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8123  -12.6194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2248  -13.3339    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   12.5103  -13.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9393  -12.9214    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6373  -14.0484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9873  -11.1905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5748  -11.9049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5748  -10.4760    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7498  -10.4760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9873   -9.7615    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5748   -9.0470    0.0000 O   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  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 22 35  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 31  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 27 30  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 35 36  1  6  0  0  0
M  END


  Mrv0541 02251208152D          

 36 36  0  0  1  0            999 V2000
   15.6998  -19.0497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -18.3353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -17.6208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -16.9063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -16.1918    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -15.4773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -14.7629    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -14.0484    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -13.3339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -12.6194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -11.9049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873  -11.1905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998  -10.4760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873   -9.7615    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.6998   -9.0470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2873   -8.3326    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.6998   -7.6181    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.4623   -8.3326    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.0498   -7.6181    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.0498   -9.0470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2248   -9.0470    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8123   -9.7615    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.2248  -10.4760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8123  -11.1905    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.2248  -11.9049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8123  -12.6194    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2248  -13.3339    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   12.5103  -13.7464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9393  -12.9214    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.6373  -14.0484    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9873  -11.1905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5748  -11.9049    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5748  -10.4760    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.7498  -10.4760    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9873   -9.7615    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.5748   -9.0470    0.0000 O   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  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  0  0  0  0
 22 35  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 31  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 27 30  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
 35 36  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0339167

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C24H47NO10S/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(26)18(25)16-33-24-23(29)22(28)21(27)20(35-24)17-34-36(30,31)32/h14-15,18-24,26-29H,2-13,16-17,25H2,1H3,(H,30,31,32)/b15-14+/t18-,19+,20-,21?,22+,23-,24-/m0/s1

> <INCHI_KEY>
UIEYIJKBVSNMMH-BHEXUNOXSA-N

> <FORMULA>
C24H47NO10S

> <MOLECULAR_WEIGHT>
541.696

> <EXACT_MASS>
541.292067419

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_AVERAGE_POLARIZABILITY>
59.34035839866184

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2S,4R,5S,6S)-6-{[(2S,3R,4E)-2-amino-3-hydroxyoctadec-4-en-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid

> <ALOGPS_LOGP>
1.69

> <JCHEM_LOGP>
1.8412105327983717

> <ALOGPS_LOGS>
-3.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.20801154571436

> <JCHEM_PKA_STRONGEST_ACIDIC>
-1.9125406784438166

> <JCHEM_PKA_STRONGEST_BASIC>
9.121807002898175

> <JCHEM_POLAR_SURFACE_AREA>
188.99999999999997

> <JCHEM_REFRACTIVITY>
134.2971

> <JCHEM_ROTATABLE_BOND_COUNT>
20

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.86e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2S,4R,5S,6S)-6-{[(2S,3R,4E)-2-amino-3-hydroxyoctadec-4-en-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxysulfonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-FEB-12         0                                  
HETATM    1  C   UNK     0      29.306 -35.559   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      28.536 -34.226   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      29.306 -32.892   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      28.536 -31.558   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      29.306 -30.225   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      28.536 -28.891   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      29.306 -27.557   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      28.536 -26.224   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      29.306 -24.890   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      28.536 -23.556   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      29.306 -22.222   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      28.536 -20.889   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      29.306 -19.555   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      28.536 -18.221   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      29.306 -16.888   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      28.536 -15.554   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      29.306 -14.220   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      26.996 -15.554   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      26.226 -14.220   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      26.226 -16.888   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      24.686 -16.888   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      23.916 -18.221   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      24.686 -19.555   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      23.916 -20.889   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      24.686 -22.222   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      23.916 -23.556   0.000  0.00  0.00           O+0
HETATM   27  S   UNK     0      24.686 -24.890   0.000  0.00  0.00           S+0
HETATM   28  O   UNK     0      23.353 -25.660   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      26.020 -24.120   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      25.456 -26.224   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      22.376 -20.889   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      21.606 -22.222   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      21.606 -19.555   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      20.066 -19.555   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      22.376 -18.221   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      21.606 -16.888   0.000  0.00  0.00           O+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   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   35                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   31                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27                                                            
CONECT   31   24   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34   35                                                  
CONECT   34   33                                                            
CONECT   35   22   33   36                                                  
CONECT   36   35                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   72    0
END

View in JSmol

Synonyms

Value	Source
Psychosine sulfuric acid	Generator
Psychosine sulphate	Generator
Psychosine sulphuric acid	Generator
{[(2S,4R,5S,6S)-6-{[(2S,3R,4E)-2-amino-3-hydroxyoctadec-4-en-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonate	Generator
{[(2S,4R,5S,6S)-6-{[(2S,3R,4E)-2-amino-3-hydroxyoctadec-4-en-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}sulphonate	Generator
{[(2S,4R,5S,6S)-6-{[(2S,3R,4E)-2-amino-3-hydroxyoctadec-4-en-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}sulphonic acid	Generator

Chemical Formula

C₂₄H₄₇NO₁₀S

Average Mass

541.6960 Da

Monoisotopic Mass

541.29207 Da

IUPAC Name

{[(2S,4R,5S,6S)-6-{[(2S,3R,4E)-2-amino-3-hydroxyoctadec-4-en-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}sulfonic acid

Traditional Name

[(2S,4R,5S,6S)-6-{[(2S,3R,4E)-2-amino-3-hydroxyoctadec-4-en-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxysulfonic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C24H47NO10S/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19(26)18(25)16-33-24-23(29)22(28)21(27)20(35-24)17-34-36(30,31)32/h14-15,18-24,26-29H,2-13,16-17,25H2,1H3,(H,30,31,32)/b15-14+/t18-,19+,20-,21?,22+,23-,24-/m0/s1

InChI Key

UIEYIJKBVSNMMH-BHEXUNOXSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

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
Monosaccharide sulfate
Monosaccharide
Oxane
Sulfuric acid monoester
Sulfate-ester
Fatty acyl
Alkyl sulfate
Sulfuric acid ester
Organic sulfuric acid or derivatives
Secondary alcohol
Organoheterocyclic compound
Polyol
Acetal
Oxacycle
Organopnictogen compound
Organonitrogen compound
Organooxygen compound
Primary aliphatic amine
Hydrocarbon derivative
Organic oxide
Alcohol
Organic nitrogen compound
Amine
Primary amine
Organic oxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.69	ALOGPS
logP	1.84	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	-1.9	ChemAxon
pKa (Strongest Basic)	9.12	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	189 Å²	ChemAxon
Rotatable Bond Count	20	ChemAxon
Refractivity	134.3 m³·mol⁻¹	ChemAxon
Polarizability	59.34 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

HMDB0013046

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB029269

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C02744

BioCyc ID

CPD-518

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53481594

PDB ID

Not Available

ChEBI ID

17507

Good Scents ID

Not Available

References

General References

Showing NP-Card for Psychosine sulfate (NP0339167)

MOL for NP0339167 (Psychosine sulfate)

3D MOL for NP0339167 (Psychosine sulfate)

3D SDF for NP0339167 (Psychosine sulfate)

3D-SDF for NP0339167 (Psychosine sulfate)

PDB for NP0339167 (Psychosine sulfate)

3D PDB for NP0339167 (Psychosine sulfate)

SMILES for NP0339167 (Psychosine sulfate)

INCHI for NP0339167 (Psychosine sulfate)

Structure for NP0339167 (Psychosine sulfate)

3D Structure for NP0339167 (Psychosine sulfate)