Np mrd loader

Showing NP-Card for PE(O-16:1(1Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) (NP0334194)

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Record Information
Version2.0
Created at2024-09-09 22:35:12 UTC
Updated at2024-09-09 22:35:12 UTC
NP-MRD IDNP0334194
Secondary Accession NumbersNone
Natural Product Identification
Common NamePE(O-16:1(1Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z))
DescriptionA class of glycerophospholipid in which a phosphorylethanolamine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphocholines can have many different combinations of fatty acids of varying lengths and saturation attached at the SN-1 and SN-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. (LipidMAPS) PE(dm16:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) is a phosphatidylethanolamine (PE or GPEtn). It is a glycerophospholipid in which a phosphorylethanolamine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphoethanolamines can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PE(dm16:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z)), in particular, consists of one chain of plasmalogen 16:0 At the C-1 position and one chain of docosahexaenoic acid at the C-2 position. The plasmalogen 16:0 Moiety is derived from animal fats, liver and kidney, while the docosahexaenoic acid moiety is derived from fish oils. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling. While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PEs are neutral zwitterions at physiological pH. They mostly have palmitic or stearic acid on carbon 1 and a long chain unsaturated fatty acid (e.G. 18:2, 20:4 And 22:6) On carbon 2. PE synthesis can occur via two pathways. The first requires that ethanolamine be activated by phosphorylation and then coupled to CDP. The ethanolamine is then transferred from CDP-ethanolamine to phosphatidic acid to yield PE. The second involves the decarboxylation of PS. Plasmalogens are glycerol ether phospholipids. They are of two types, alkyl ether (-O-CH2-) and alkenyl ether (-O-CH=CH-). Dihydroxyacetone phosphate (DHAP) serves as the glycerol precursor for the synthesis of plasmalogens. Three major classes of plasmalogens have been identified: Choline, ethanolamine and serine derivatives. Ethanolamine plasmalogen is prevalent in myelin. Choline plasmalogen is abundant in cardiac tissue. Usually, the highest proportion of the plasmalogen form is in the ethanolamine class with rather less in choline, and commonly little or none in other phospholipids such as phosphatidylinositol. In choline plasmalogens of most tissues, a higher proportion is often of the O-alkyl rather than the O-alkenyl form, but the reverse tends to be true in heart lipids. In animal tissues, the alkyl and alkenyl moieties in both non-polar and phospholipids tend to be rather simple in composition with 16:0, 18:0 And 18:1 (Double bond in position 9) predominating. Ether analogues of triacylglycerols, i.E. 1-Alkyldiacyl-sn-glycerols, are present at trace levels only if at all in most animal tissues, but they can be major components of some marine lipids. [HMDB]
Structure
Thumb
MOLSDFPDBSMILESInChI

MOL for NP0334194 (PE(O-16:1(1Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)))


  Mrv1572004261606452D          

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M  END
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3D MOL for NP0334194 (PE(O-16:1(1Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)))

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3D SDF for NP0334194 (PE(O-16:1(1Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)))

  Mrv1572004261606452D          

 67 66  0  0  1  0            999 V2000
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 32 30  2  0  0  0  0
 33 31  1  0  0  0  0
 34 32  1  0  0  0  0
 35 33  1  0  0  0  0
 36 34  1  0  0  0  0
 38 35  2  0  0  0  0
 39 37  1  0  0  0  0
 42 40  1  0  0  0  0
 42 41  1  0  0  0  0
 43 36  1  0  0  0  0
 44 37  1  0  0  0  0
 45 43  2  0  0  0  0
 48 38  1  0  0  0  0
 48 40  1  0  0  0  0
 49 39  1  0  0  0  0
 50 41  1  0  0  0  0
 42 51  1  1  0  0  0
 51 43  1  0  0  0  0
 52 46  1  0  0  0  0
 52 47  2  0  0  0  0
 52 49  1  0  0  0  0
 52 50  1  0  0  0  0
 53  5  1  0  0  0  0
 54  7  1  0  0  0  0
 55 11  1  0  0  0  0
 56 13  1  0  0  0  0
 57 17  1  0  0  0  0
 58 19  1  0  0  0  0
 59 21  1  0  0  0  0
 60 22  1  0  0  0  0
 61 24  1  0  0  0  0
 62 26  1  0  0  0  0
 63 30  1  0  0  0  0
 64 32  1  0  0  0  0
 65 35  1  0  0  0  0
 66 38  1  0  0  0  0
 42 67  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0334194

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]\C(CC)=C(\[H])C\C([H])=C(/[H])C\C([H])=C(/[H])C\C([H])=C(/[H])C\C([H])=C(/[H])C\C([H])=C(/[H])CCC(=O)O[C@]([H])(CO\C([H])=C(/[H])CCCCCCCCCCCCCC)COP(O)(=O)OCCN

> <INCHI_IDENTIFIER>
InChI=1S/C43H74NO7P/c1-3-5-7-9-11-13-15-17-19-20-21-22-23-24-26-28-30-32-34-36-43(45)51-42(41-50-52(46,47)49-39-37-44)40-48-38-35-33-31-29-27-25-18-16-14-12-10-8-6-4-2/h5,7,11,13,17,19,21-22,24,26,30,32,35,38,42H,3-4,6,8-10,12,14-16,18,20,23,25,27-29,31,33-34,36-37,39-41,44H2,1-2H3,(H,46,47)/b7-5+,13-11+,19-17+,22-21+,26-24+,32-30+,38-35+/t42-/m1/s1

> <INCHI_KEY>
WVGALBKSWOUIEZ-DLYXUNISSA-N

> <FORMULA>
C43H74NO7P

> <MOLECULAR_WEIGHT>
748.039

> <EXACT_MASS>
747.520290725

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
126

> <JCHEM_AVERAGE_POLARIZABILITY>
90.75287453087466

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-aminoethoxy)[(2R)-2-[(4E,7E,10E,13E,16E,19E)-docosa-4,7,10,13,16,19-hexaenoyloxy]-3-[(1E)-hexadec-1-en-1-yloxy]propoxy]phosphinic acid

> <ALOGPS_LOGP>
9.06

> <JCHEM_LOGP>
11.339572050116608

> <ALOGPS_LOGS>
-7.04

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8688005889911472

> <JCHEM_PKA_STRONGEST_BASIC>
9.999929336362282

> <JCHEM_POLAR_SURFACE_AREA>
117.31000000000003

> <JCHEM_REFRACTIVITY>
225.64800000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
38

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.85e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-aminoethoxy((2R)-2-[(4E,7E,10E,13E,16E,19E)-docosa-4,7,10,13,16,19-hexaenoyloxy]-3-[(1E)-hexadec-1-en-1-yloxy]propoxy)phosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

Download
3D-SDF for NP0334194 (PE(O-16:1(1Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)))
Download
PDB for NP0334194 (PE(O-16:1(1Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)))
HEADER    PROTEIN                                 26-APR-16   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-16         0                                  
HETATM    1  C   UNK     0      41.867 -19.552   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.526  -8.772   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      43.201 -20.322   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.860  -8.002   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      44.535 -19.552   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.194  -8.772   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      45.868 -20.322   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.527  -8.002   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      47.202 -19.552   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      17.861  -8.772   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      47.202 -18.012   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      19.195  -8.002   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      48.536 -17.242   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      20.528  -8.772   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      48.536 -15.702   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      21.862  -8.002   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      47.202 -14.932   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      23.196  -8.772   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      47.202 -13.392   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      45.868 -12.622   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      44.535 -13.392   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      43.201 -12.622   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      41.867 -13.392   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      41.867 -14.932   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      24.529  -8.002   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      40.534 -15.702   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      25.863  -8.772   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      40.534 -17.242   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      27.197  -8.002   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      39.200 -18.012   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      28.530  -8.772   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      37.866 -17.242   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      29.864  -8.002   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      36.533 -18.012   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      31.198  -8.772   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      35.199 -17.242   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      37.096  -8.621   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      31.198 -10.312   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      37.866  -9.955   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      32.532 -12.622   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      35.199 -12.622   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      33.865 -13.392   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      35.199 -15.702   0.000  0.00  0.00           C+0
HETATM   44  N   UNK     0      37.866  -7.287   0.000  0.00  0.00           N+0
HETATM   45  O   UNK     0      36.533 -14.932   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      38.636 -13.956   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0      39.200 -11.852   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0      32.532 -11.082   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      37.096 -11.288   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      36.533 -13.392   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      33.865 -14.932   0.000  0.00  0.00           O+0
HETATM   52  P   UNK     0      37.866 -12.622   0.000  0.00  0.00           P+0
HETATM   53  H   UNK     0      44.535 -18.012   0.000  0.00  0.00           H+0
HETATM   54  H   UNK     0      45.868 -21.862   0.000  0.00  0.00           H+0
HETATM   55  H   UNK     0      45.868 -17.242   0.000  0.00  0.00           H+0
HETATM   56  H   UNK     0      49.869 -18.012   0.000  0.00  0.00           H+0
HETATM   57  H   UNK     0      45.868 -15.702   0.000  0.00  0.00           H+0
HETATM   58  H   UNK     0      48.536 -12.622   0.000  0.00  0.00           H+0
HETATM   59  H   UNK     0      44.535 -14.932   0.000  0.00  0.00           H+0
HETATM   60  H   UNK     0      43.201 -11.082   0.000  0.00  0.00           H+0
HETATM   61  H   UNK     0      43.201 -15.702   0.000  0.00  0.00           H+0
HETATM   62  H   UNK     0      39.200 -14.932   0.000  0.00  0.00           H+0
HETATM   63  H   UNK     0      39.200 -19.552   0.000  0.00  0.00           H+0
HETATM   64  H   UNK     0      37.866 -15.702   0.000  0.00  0.00           H+0
HETATM   65  H   UNK     0      32.532  -8.002   0.000  0.00  0.00           H+0
HETATM   66  H   UNK     0      29.864 -11.082   0.000  0.00  0.00           H+0
HETATM   67  H   UNK     0      33.865 -11.852   0.000  0.00  0.00           H+0
CONECT    1    3                                                            
CONECT    2    4                                                            
CONECT    3    1    5                                                       
CONECT    4    2    6                                                       
CONECT    5    3    7   53                                                  
CONECT    6    4    8                                                       
CONECT    7    5    9   54                                                  
CONECT    8    6   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   13   55                                                  
CONECT   12   10   14                                                       
CONECT   13   11   15   56                                                  
CONECT   14   12   16                                                       
CONECT   15   13   17                                                       
CONECT   16   14   18                                                       
CONECT   17   15   19   57                                                  
CONECT   18   16   25                                                       
CONECT   19   17   20   58                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   59                                                  
CONECT   22   21   23   60                                                  
CONECT   23   22   24                                                       
CONECT   24   23   26   61                                                  
CONECT   25   18   27                                                       
CONECT   26   24   28   62                                                  
CONECT   27   25   29                                                       
CONECT   28   26   30                                                       
CONECT   29   27   31                                                       
CONECT   30   28   32   63                                                  
CONECT   31   29   33                                                       
CONECT   32   30   34   64                                                  
CONECT   33   31   35                                                       
CONECT   34   32   36                                                       
CONECT   35   33   38   65                                                  
CONECT   36   34   43                                                       
CONECT   37   39   44                                                       
CONECT   38   35   48   66                                                  
CONECT   39   37   49                                                       
CONECT   40   42   48                                                       
CONECT   41   42   50                                                       
CONECT   42   40   41   51   67                                             
CONECT   43   36   45   51                                                  
CONECT   44   37                                                            
CONECT   45   43                                                            
CONECT   46   52                                                            
CONECT   47   52                                                            
CONECT   48   38   40                                                       
CONECT   49   39   52                                                       
CONECT   50   41   52                                                       
CONECT   51   42   43                                                       
CONECT   52   46   47   49   50                                             
CONECT   53    5                                                            
CONECT   54    7                                                            
CONECT   55   11                                                            
CONECT   56   13                                                            
CONECT   57   17                                                            
CONECT   58   19                                                            
CONECT   59   21                                                            
CONECT   60   22                                                            
CONECT   61   24                                                            
CONECT   62   26                                                            
CONECT   63   30                                                            
CONECT   64   32                                                            
CONECT   65   35                                                            
CONECT   66   38                                                            
CONECT   67   42                                                            
MASTER        0    0    0    0    0    0    0    0   67    0  132    0
END

Download
3D PDB for NP0334194 (PE(O-16:1(1Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)))
Download
SMILES for NP0334194 (PE(O-16:1(1Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)))
[H]\C(CC)=C(\[H])C\C([H])=C(/[H])C\C([H])=C(/[H])C\C([H])=C(/[H])C\C([H])=C(/[H])C\C([H])=C(/[H])CCC(=O)O[C@]([H])(CO\C([H])=C(/[H])CCCCCCCCCCCCCC)COP(O)(=O)OCCN
Download
INCHI for NP0334194 (PE(O-16:1(1Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)))
InChI=1S/C43H74NO7P/c1-3-5-7-9-11-13-15-17-19-20-21-22-23-24-26-28-30-32-34-36-43(45)51-42(41-50-52(46,47)49-39-37-44)40-48-38-35-33-31-29-27-25-18-16-14-12-10-8-6-4-2/h5,7,11,13,17,19,21-22,24,26,30,32,35,38,42H,3-4,6,8-10,12,14-16,18,20,23,25,27-29,31,33-34,36-37,39-41,44H2,1-2H3,(H,46,47)/b7-5+,13-11+,19-17+,22-21+,26-24+,32-30+,38-35+/t42-/m1/s1
Download
View in JSmol
SynonymsNot Available
Chemical FormulaC43H74NO7P
Average Mass748.0390 Da
Monoisotopic Mass747.52029 Da
IUPAC Name(2-aminoethoxy)[(2R)-2-[(4E,7E,10E,13E,16E,19E)-docosa-4,7,10,13,16,19-hexaenoyloxy]-3-[(1E)-hexadec-1-en-1-yloxy]propoxy]phosphinic acid
Traditional Name2-aminoethoxy((2R)-2-[(4E,7E,10E,13E,16E,19E)-docosa-4,7,10,13,16,19-hexaenoyloxy]-3-[(1E)-hexadec-1-en-1-yloxy]propoxy)phosphinic acid
CAS Registry NumberNot Available
SMILES
[H]\C(CC)=C(\[H])C\C([H])=C(/[H])C\C([H])=C(/[H])C\C([H])=C(/[H])C\C([H])=C(/[H])C\C([H])=C(/[H])CCC(=O)O[C@]([H])(CO\C([H])=C(/[H])CCCCCCCCCCCCCC)COP(O)(=O)OCCN
InChI Identifier
InChI=1S/C43H74NO7P/c1-3-5-7-9-11-13-15-17-19-20-21-22-23-24-26-28-30-32-34-36-43(45)51-42(41-50-52(46,47)49-39-37-44)40-48-38-35-33-31-29-27-25-18-16-14-12-10-8-6-4-2/h5,7,11,13,17,19,21-22,24,26,30,32,35,38,42H,3-4,6,8-10,12,14-16,18,20,23,25,27-29,31,33-34,36-37,39-41,44H2,1-2H3,(H,46,47)/b7-5+,13-11+,19-17+,22-21+,26-24+,32-30+,38-35+/t42-/m1/s1
InChI KeyWVGALBKSWOUIEZ-DLYXUNISSA-N
Experimental Spectra
Not Available
Predicted Spectra
Not Available
Chemical Shift Submissions
Not Available
Species
Species of OriginNot Available
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 1-(1z-alkenyl),2-acylglycerophosphoethanolamines. These are glycerophosphoethanolamines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position,  and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
KingdomOrganic compounds  
Super ClassLipids and lipid-like molecules  
ClassGlycerophospholipids  
Sub ClassGlycerophosphoethanolamines  
Direct Parent1-(1Z-alkenyl),2-acylglycerophosphoethanolamines  
Alternative Parents
Substituents
  • 1-(1z-alkenyl),2-acylglycerophosphoethanolamine
    • 

  • Glycerol vinyl ether
    • 

  • Phosphoethanolamine
    • 

  • Dialkyl phosphate
    • 

  • Fatty acid ester
    • 

  • Fatty acyl
    • 

  • Alkyl phosphate
    • 

  • Phosphoric acid ester
    • 

  • Organic phosphoric acid derivative
    • 

  • Carboxylic acid ester
    • 

  • Amino acid or derivatives
    • 

  • Monocarboxylic acid or derivatives
    • 

  • Carboxylic acid derivative
    • 

  • Organic nitrogen compound
    • 

  • Organic oxygen compound
    • 

  • Organopnictogen compound
    • 

  • Organic oxide
    • 

  • Hydrocarbon derivative
    • 

  • Primary amine
    • 

  • Organooxygen compound
    • 

  • Organonitrogen compound
    • 

  • Primary aliphatic amine
    • 

  • Carbonyl group
    • 

  • Amine
    • 

  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP9.06ALOGPS
logP11.34ChemAxon
logS-7ALOGPS
pKa (Strongest Acidic)1.87ChemAxon
pKa (Strongest Basic)10ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area117.31 ŲChemAxon
Rotatable Bond Count38ChemAxon
Refractivity225.65 m³·mol⁻¹ChemAxon
Polarizability90.75 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound134777291  
PDB IDNot Available
ChEBI IDNot Available
Good Scents IDNot Available
References
General ReferencesNot Available