MiMeDB: Showing metabocard for 2-Acyl-sn-glycero-3-phosphoethanolamine (N-C18:1) (MMDBc0031562)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-18 01:39:17 UTC

Update Date

2022-08-31 18:21:48 UTC

MiMeDB ID

MMDBc0031562

Metabolite Identification

Common Name

2-Acyl-sn-glycero-3-phosphoethanolamine (N-C18:1)

Description

2-acyl-sn-glycero-3-phosphoethanolamine (n-c18:1) belongs to the class of Lysophosphatidylethanolamines. These are glycerophosphoetahnolamines (molecules containing an ethanolamine moiety attached to the phosphate group linked to a glycerol) with one saturated fatty acid bonded to the glycerol moiety through an ester linkage. (inferred from compound structure)

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 08141218052D          

 34 33  0  0  0  0            999 V2000
    4.1343    8.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0060    8.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6476    7.5731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5193    6.7581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1609    6.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0326    5.4245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6742    4.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5459    4.0910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9574    3.8687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5991    3.3501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3690    3.6464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0106    3.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7805    3.4242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4222    2.9056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1921    3.2019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8337    2.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1215    1.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4799    1.7943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1435    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6568    2.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0152    2.7574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6036    2.9797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8915    1.5720    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.9134    3.8687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7320    3.7946    0.0000 O   0  3  0  0  0  0  0  0  0  0  0  0
   15.5497    1.3749    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   16.5870    2.6581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7100    1.4979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4267    2.5351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2453    2.4610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0684    2.0165    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    6.4441    5.2023    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7759    3.7946    0.0000 H   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  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  2  0  0  0  0
  9  8  1  0  0  0  0
 10  9  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
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 19 18  1  0  0  0  0
 22 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 17  1  0  0  0  0
 24 18  1  0  0  0  0
 25 20  1  0  0  0  0
 26 23  2  0  0  0  0
 29 19  1  0  0  0  0
 30 21  1  0  0  0  0
 31 22  1  0  0  0  0
 31 23  1  0  0  0  0
 32 27  1  0  0  0  0
 32 28  2  0  0  0  0
 32 29  1  0  0  0  0
 32 30  1  0  0  0  0
 33  7  1  0  0  0  0
 34  8  1  0  0  0  0
M  CHG  2  26   1  27  -1
M  RAD  2  24   3  26   2
M  END


  Mrv0541 08141218052D          

 34 33  0  0  0  0            999 V2000
    4.1343    8.9066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0060    8.0917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6476    7.5731    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5193    6.7581    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1609    6.2395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0326    5.4245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6742    4.9059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5459    4.0910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9574    3.8687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5991    3.3501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3690    3.6464    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0106    3.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7805    3.4242    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4222    2.9056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1921    3.2019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8337    2.6833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1215    1.2757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4799    1.7943    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1435    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6568    2.2388    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0152    2.7574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6036    2.9797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8915    1.5720    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.9134    3.8687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7320    3.7946    0.0000 O   0  3  0  0  0  0  0  0  0  0  0  0
   15.5497    1.3749    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   16.5870    2.6581    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7100    1.4979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.4267    2.5351    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2453    2.4610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0684    2.0165    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    6.4441    5.2023    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7759    3.7946    0.0000 H   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  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  2  0  0  0  0
  9  8  1  0  0  0  0
 10  9  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
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 16  1  0  0  0  0
 19 18  1  0  0  0  0
 22 20  1  0  0  0  0
 22 21  1  0  0  0  0
 23 17  1  0  0  0  0
 24 18  1  0  0  0  0
 25 20  1  0  0  0  0
 26 23  2  0  0  0  0
 29 19  1  0  0  0  0
 30 21  1  0  0  0  0
 31 22  1  0  0  0  0
 31 23  1  0  0  0  0
 32 27  1  0  0  0  0
 32 28  2  0  0  0  0
 32 29  1  0  0  0  0
 32 30  1  0  0  0  0
 33  7  1  0  0  0  0
 34  8  1  0  0  0  0
M  CHG  2  26   1  27  -1
M  RAD  2  24   3  26   2
M  END
> <DATABASE_ID>
MMDBc0031562

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(CCCCCC)=C(\[H])CCCCCCCCCC(=[O+])OC(CO)COP([O-])(=O)OCC[N]

> <INCHI_IDENTIFIER>
InChI=1S/C23H44NO7P/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/h7-8,22,25H,2-6,9-21H2,1H3,(H,27,28)/q+1/p-1/b8-7+

> <INCHI_KEY>
QLFHRWIZXUHUNT-BQYQJAHWSA-M

> <FORMULA>
C23H43NO7P

> <MOLECULAR_WEIGHT>
476.5638

> <EXACT_MASS>
476.277714247

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
54.78488270944826

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{2-[(3-hydroxy-2-{[(11E)-1-(λ³-oxidanyliumylidene)octadec-11-en-1-yl]oxy}propyl phosphonato)oxy]ethyl}azanylidene

> <ALOGPS_LOGP>
5.43

> <JCHEM_LOGP>
4.182069338187556

> <ALOGPS_LOGS>
-5.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.283887912587161

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8744572379820568

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1129600199213128

> <JCHEM_POLAR_SURFACE_AREA>
105.12000000000002

> <JCHEM_REFRACTIVITY>
125.08729999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
24

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.27e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{2-[(3-hydroxy-2-{[(11E)-1-(λ³-oxidanyliumylidene)octadec-11-en-1-yl]oxy}propyl phosphonato)oxy]ethyl}azanylidene

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 14-AUG-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   14-AUG-12         0                                  
HETATM    1  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   24  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   25  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+1
HETATM   27  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O-1
HETATM   28  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   32  P   UNK     0       0.000   0.000   0.000  0.00  0.00           P+0
HETATM   33  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.000   0.000   0.000  0.00  0.00           H+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   33                                                  
CONECT    8    7    9   34                                                  
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   23                                                       
CONECT   18   19   24                                                       
CONECT   19   18   29                                                       
CONECT   20   22   25                                                       
CONECT   21   22   30                                                       
CONECT   22   20   21   31                                                  
CONECT   23   17   26   31                                                  
CONECT   24   18                                                            
CONECT   25   20                                                            
CONECT   26   23                                                            
CONECT   27   32                                                            
CONECT   28   32                                                            
CONECT   29   19   32                                                       
CONECT   30   21   32                                                       
CONECT   31   22   23                                                       
CONECT   32   27   28   29   30                                             
CONECT   33    7                                                            
CONECT   34    8                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   66    0
END

Synonyms

Not Available

Chemical Formula

C₂₃H₄₃NO₇P

Average Molecular Weight

476.5638

Monoisotopic Molecular Weight

476.277714247

IUPAC Name

{2-[(3-hydroxy-2-{[(11E)-1-(λ³-oxidanyliumylidene)octadec-11-en-1-yl]oxy}propyl phosphonato)oxy]ethyl}azanylidene

Traditional Name

{2-[(3-hydroxy-2-{[(11E)-1-(λ³-oxidanyliumylidene)octadec-11-en-1-yl]oxy}propyl phosphonato)oxy]ethyl}azanylidene

CAS Registry Number

Not Available

SMILES

[H]\C(CCCCCC)=C(\[H])CCCCCCCCCC(=[O+])OC(CO)COP([O-])(=O)OCC[N]

InChI Identifier

InChI=1S/C23H44NO7P/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/h7-8,22,25H,2-6,9-21H2,1H3,(H,27,28)/q+1/p-1/b8-7+

InChI Key

QLFHRWIZXUHUNT-BQYQJAHWSA-M

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glycerophospholipids. These are derivatives of glycerophosphoric acid that contains at least one O-acyl, or O-alkyl, or O-(1-alkenyl) group attached to the glycerol residue.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Not Available

Direct Parent

Glycerophospholipids

Alternative Parents

Substituents

Glycerophospholipid
Dialkyl phosphate
Fatty acid ester
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Carboxylic acid ester
Organic nitrene
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic zwitterion
Primary alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.0043 g/L	ALOGPS
logP	5.43	ALOGPS
logP	4.18	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	1.87	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	105.12 Å²	ChemAxon
Rotatable Bond Count	24	ChemAxon
Refractivity	125.09 m³·mol⁻¹	ChemAxon
Polarizability	54.78 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

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-004i-2330900000-a3d48d7caa7f5fb9c4c5	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-002o-2910300000-73f01b0ad7102ea84a03	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-001r-9480000000-091f345f216d28135d24	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0006-9100200000-2e49a82cddc883839647	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0006-9010000000-ffd5d62a54ff20361764	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0006-9000000000-72dc2ee436ea3b2c2df8	2015-09-15	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Proteins

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Related Health Condition	Evidence Type	Measured in Matrix	Data Source	Reference

Microbial Sources

Phylum	Total species	Hosts and Body Sites	Microbial Links
Proteobacteria	129	Human Feces; Human	Unknown; Metabolic reconstruction
Firmicutes	265	Human Feces; Human	Metabolic reconstruction
Actinobacteria	109	Human Feces; Human	Metabolic reconstruction
Bacteroidetes	20	Human Feces; Human	Metabolic reconstruction
Spirochaetes	1	Human Feces	Metabolic reconstruction
Thaumarchaeota	1	Human Feces	Metabolic reconstruction
Fusobacteria	4	Human Feces; Human	Metabolic reconstruction
Planctomycetes	1	Human Feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference	Details

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference
Human Feces	Detected but not Quantified									HMDB		details

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB 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

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Noronha A, Modamio J, Jarosz Y, Guerard E, Sompairac N, Preciat G, Danielsdottir AD, Krecke M, Merten D, Haraldsdottir HS, Heinken A, Heirendt L, Magnusdottir S, Ravcheev DA, Sahoo S, Gawron P, Friscioni L, Garcia B, Prendergast M, Puente A, Rodrigues M, Roy A, Rouquaya M, Wiltgen L, Zagare A, John E, Krueger M, Kuperstein I, Zinovyev A, Schneider R, Fleming RMT, Thiele I: The Virtual Metabolic Human database: integrating human and gut microbiome metabolism with nutrition and disease. Nucleic Acids Res. 2019 Jan 8;47(D1):D614-D624. doi: 10.1093/nar/gky992. [PubMed:30371894 ]

Showing metabocard for 2-Acyl-sn-glycero-3-phosphoethanolamine (N-C18:1) (MMDBc0031562)

MOL for #<Metabolite:0x00007f45741a99e0>

3D MOL for #<Metabolite:0x00007f45741a99e0>

3D SDF for #<Metabolite:0x00007f45741a99e0>

3D-SDF for #<Metabolite:0x00007f45741a99e0>

PDB for #<Metabolite:0x00007f45741a99e0>

3D PDB for #<Metabolite:0x00007f45741a99e0>

SMILES for #<Metabolite:0x00007f45741a99e0>

INCHI for #<Metabolite:0x00007f45741a99e0>

Structure for #<Metabolite:0x00007f45741a99e0>

3D Structure for #<Metabolite:0x00007f45741a99e0>