NP-MRD: Showing NP-Card for LysoPE(0:0/18:0) (NP0091141)

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Record Information

Version

2.0

Created at

2022-05-11 18:31:48 UTC

Updated at

2022-05-11 18:31:48 UTC

NP-MRD ID

NP0091141

Secondary Accession Numbers

None

Natural Product Identification

Common Name

LysoPE(0:0/18:0)

Description

PE(0:0/18:0) Is a phosphatidylethanolamine. 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 to the C-1 and C-2 positions. PE(0:0/18:0), In particular, consists of two octadecanoyl chains at positions C-1 and C-2. 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.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 02241201202D          

 33 32  0  0  1  0            999 V2000
   21.2599   -2.9899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.5848   -3.3797    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   19.9097   -2.9899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9350   -3.3797    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2345   -3.3797    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0580   -4.1593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.6101   -2.9899    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   22.2204   -2.3147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.9999   -3.6650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.2852   -2.6001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.9603   -2.9899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.6355   -2.6001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3106   -2.9899    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   21.1725   -4.1890    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1974   -4.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9119   -4.5718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6264   -4.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3408   -4.5717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0553   -4.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7698   -4.5717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4843   -4.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.1988   -4.5717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9132   -4.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6277   -4.5717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3422   -4.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0566   -4.5717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7712   -4.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4856   -4.5717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2001   -4.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9146   -4.5717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6290   -4.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3435   -4.5717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3435   -5.3968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  1  1  0  0  0  0
  5  3  1  0  0  0  0
  2  6  1  6  0  0  0
  7  4  1  0  0  0  0
  8  7  2  0  0  0  0
  9  7  1  0  0  0  0
 10  7  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
  2 14  1  1  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24 23  1  0  0  0  0
 25 24  1  0  0  0  0
 26 25  1  0  0  0  0
 27 26  1  0  0  0  0
 28 27  1  0  0  0  0
 29 28  1  0  0  0  0
 30 29  1  0  0  0  0
 31 30  1  0  0  0  0
 32 31  1  0  0  0  0
 33 32  2  0  0  0  0
  6 32  1  0  0  0  0
M  END

     RDKit          3D

 80 79  0  0  0  0  0  0  0  0999 V2000
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    6.3902    1.2707    0.4581 C   0  0  2  0  0  0  0  0  0  0  0  0
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    8.5188    2.1396    1.0798 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1034    0.3161   -0.4565 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.7529    0.2229   -2.8754 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3570    0.0710   -1.0667 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1730   -0.9577   -0.1108 H   0  0  0  0  0  0  0  0  0  0  0  0
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  2 36  1  0
  2 37  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
M  END


  Mrv0541 02241201202D          

 33 32  0  0  1  0            999 V2000
   21.2599   -2.9899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.5848   -3.3797    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   19.9097   -2.9899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9350   -3.3797    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.2345   -3.3797    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0580   -4.1593    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.6101   -2.9899    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   22.2204   -2.3147    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.9999   -3.6650    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.2852   -2.6001    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.9603   -2.9899    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   25.3106   -2.9899    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   21.1725   -4.1890    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   16.4856   -4.5717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   17.9146   -4.5717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   19.3435   -5.3968    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 18 17  1  0  0  0  0
 19 18  1  0  0  0  0
 20 19  1  0  0  0  0
 21 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 22  1  0  0  0  0
 24 23  1  0  0  0  0
 25 24  1  0  0  0  0
 26 25  1  0  0  0  0
 27 26  1  0  0  0  0
 28 27  1  0  0  0  0
 29 28  1  0  0  0  0
 30 29  1  0  0  0  0
 31 30  1  0  0  0  0
 32 31  1  0  0  0  0
 33 32  2  0  0  0  0
  6 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0091141

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@](CO)(COP(O)(=O)OCCN)OC(=O)CCCCCCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C23H48NO7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-23(26)31-22(20-25)21-30-32(27,28)29-19-18-24/h22,25H,2-21,24H2,1H3,(H,27,28)/t22-/m1/s1

> <INCHI_KEY>
KIHAGWUUUHJRMS-JOCHJYFZSA-N

> <FORMULA>
C23H48NO7P

> <MOLECULAR_WEIGHT>
481.6035

> <EXACT_MASS>
481.316839407

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
56.554014981328024

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-aminoethoxy)[(2R)-3-hydroxy-2-(octadecanoyloxy)propoxy]phosphinic acid

> <ALOGPS_LOGP>
4.74

> <JCHEM_LOGP>
4.418998785327011

> <ALOGPS_LOGS>
-5.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.579269652388977

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8688048676175866

> <JCHEM_PKA_STRONGEST_BASIC>
9.999917895738319

> <JCHEM_POLAR_SURFACE_AREA>
128.31

> <JCHEM_REFRACTIVITY>
126.61449999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
25

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.45e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-aminoethoxy(2R)-3-hydroxy-2-(octadecanoyloxy)propoxyphosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      39.685  -5.581   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      38.425  -6.309   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      37.165  -5.581   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      40.945  -6.309   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      35.904  -6.309   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      37.442  -7.764   0.000  0.00  0.00           O+0
HETATM    7  P   UNK     0      42.206  -5.581   0.000  0.00  0.00           P+0
HETATM    8  O   UNK     0      41.478  -4.321   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      42.933  -6.841   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      43.466  -4.854   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      44.726  -5.581   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      45.986  -4.854   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      47.246  -5.581   0.000  0.00  0.00           N+0
HETATM   14  H   UNK     0      39.522  -7.819   0.000  0.00  0.00           H+0
HETATM   15  C   UNK     0      13.435  -7.764   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.769  -8.534   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      16.103  -7.764   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      17.436  -8.534   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      18.770  -7.764   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      20.104  -8.534   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      21.437  -7.764   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      22.771  -8.534   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      24.105  -7.764   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.438  -8.534   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.772  -7.764   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      28.106  -8.534   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      29.440  -7.764   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      30.773  -8.534   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      32.107  -7.764   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      33.441  -8.534   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      34.774  -7.764   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      36.108  -8.534   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      36.108 -10.074   0.000  0.00  0.00           O+0
CONECT    1    2    4                                                       
CONECT    2    1    3    6   14                                             
CONECT    3    2    5                                                       
CONECT    4    1    7                                                       
CONECT    5    3                                                            
CONECT    6    2   32                                                       
CONECT    7    4    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14    2                                                            
CONECT   15   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                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33    6                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   64    0
END

View in JSmol

Synonyms

Value	Source
octadecanoyl-lysophosphatidylethanolamine	Lipid Annotator, HMDB
1-hydroxy-2-stearoyl-sn-glycero-3-phosphoethanolamine	Lipid Annotator, HMDB
LPE(0:0/18:0)	Lipid Annotator, HMDB
Lysophosphatidylethanolamine(0:0/18:0)	Lipid Annotator, HMDB
Lysophosphatidylethanolamine(18:0)	Lipid Annotator, HMDB
Lyso-PE(0:0/18:0)	Lipid Annotator, HMDB
Lyso-PE(18:0)	Lipid Annotator, HMDB
LPE(18:0)	Lipid Annotator, HMDB
LysoPE(0:0/18:0)	Lipid Annotator
1-hydroxy-2-octadecanoyl-sn-glycero-3-phosphoethanolamine	Lipid Annotator, HMDB
LysoPE(18:0)	Lipid Annotator, HMDB
2-Stearoyl-gpe	ChEBI
2-Stearoyl-gpe (18:0)	ChEBI
2-Stearoyl-sn-glycero-3-phosphoethanolamine zwitterion	ChEBI
GPE(0:0/18:0)	ChEBI
GPE(18:0)	ChEBI
Lysophosphatidylethanolamine zwitterion (0:0/18:0)	ChEBI
Lysophosphatidylethanolamine zwitterion (18:0)	ChEBI
PE(0:0/18:0)	ChEBI
PE(18:0)	ChEBI
Phosphatidylethanolamine zwitterion (0:0/18:0)	ChEBI
Phosphatidylethanolamine zwitterion (18:0)	ChEBI
1-Hydroxyl-2-stearoyl-sn-glycero-3-phosphoethanolamine	HMDB
Stearoyl phosphatidylethanolamine	HMDB
2-Stearoyl-3-glycerylphosphorylethanolamine	HMDB
2-Stearoyl-lysophosphatidylethanolamine	HMDB
2-Stearoyl-sn-glycero-3-phosphoethanolamine	HMDB

Chemical Formula

C₂₃H₄₈NO₇P

Average Mass

481.6035 Da

Monoisotopic Mass

481.31684 Da

IUPAC Name

(2-aminoethoxy)[(2R)-3-hydroxy-2-(octadecanoyloxy)propoxy]phosphinic acid

Traditional Name

2-aminoethoxy(2R)-3-hydroxy-2-(octadecanoyloxy)propoxyphosphinic acid

CAS Registry Number

Not Available

SMILES

[H][C@@](CO)(COP(O)(=O)OCCN)OC(=O)CCCCCCCCCCCCCCCCC

InChI Identifier

InChI=1S/C23H48NO7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-23(26)31-22(20-25)21-30-32(27,28)29-19-18-24/h22,25H,2-21,24H2,1H3,(H,27,28)/t22-/m1/s1

InChI Key

KIHAGWUUUHJRMS-JOCHJYFZSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Ovis aries	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB

Chemical Taxonomy

Description

This compound belongs to the class of organic compounds known as 2-acyl-sn-glycero-3-phosphoethanolamines. These are glycerophoethanolamines in which the glycerol is esterified with a fatty acid at O-2 position, and linked at position 3 to a phosphoethanolamine.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphoethanolamines

Direct Parent

2-acyl-sn-glycero-3-phosphoethanolamines

Alternative Parents

Substituents

2-monoacyl-sn-glycero-3-phosphoethanolamine
Phosphoethanolamine
Fatty acid ester
Dialkyl phosphate
Organic phosphoric acid derivative
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Amino acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organooxygen compound
Organonitrogen compound
Hydrocarbon derivative
Alcohol
Primary aliphatic amine
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Carbonyl group
Organic oxygen compound
Amine
Primary amine
Primary alcohol
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	4.74	ALOGPS
logP	4.42	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	1.87	ChemAxon
pKa (Strongest Basic)	10	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	128.31 Å²	ChemAxon
Rotatable Bond Count	25	ChemAxon
Refractivity	126.61 m³·mol⁻¹	ChemAxon
Polarizability	56.55 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for LysoPE(0:0/18:0) (NP0091141)

MOL for NP0091141 (LysoPE(0:0/18:0))

3D MOL for NP0091141 (LysoPE(0:0/18:0))

3D SDF for NP0091141 (LysoPE(0:0/18:0))

3D-SDF for NP0091141 (LysoPE(0:0/18:0))

PDB for NP0091141 (LysoPE(0:0/18:0))

3D PDB for NP0091141 (LysoPE(0:0/18:0))

SMILES for NP0091141 (LysoPE(0:0/18:0))

INCHI for NP0091141 (LysoPE(0:0/18:0))

Structure for NP0091141 (LysoPE(0:0/18:0))

3D Structure for NP0091141 (LysoPE(0:0/18:0))