MiMeDB: Showing metabocard for 2-Acyl-sn-glycero-3-phosphoethanolamine (N-C12:0) (MMDBc0031556)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-18 01:39:03 UTC

Update Date

2022-08-31 18:21:45 UTC

Metabolite ID

MMDBc0031556

Metabolite Identification

Common Name

2-Acyl-sn-glycero-3-phosphoethanolamine (N-C12:0)

Description

2-acyl-sn-glycero-3-phosphoethanolamine (n-c12:0) 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          

 26 25  0  0  0  0            999 V2000
    4.7759    3.7946    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  0  0  0  0  0  0  0  0  0  0  0
   15.5497    1.3749    0.0000 O   0  0  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
  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  1  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
 13 12  1  0  0  0  0
 16 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 11  1  0  0  0  0
 18 12  1  0  0  0  0
 19 14  1  0  0  0  0
 20 17  2  0  0  0  0
 23 13  1  0  0  0  0
 24 15  1  0  0  0  0
 25 16  1  0  0  0  0
 25 17  1  0  0  0  0
 26 21  1  0  0  0  0
 26 22  2  0  0  0  0
 26 23  1  0  0  0  0
 26 24  1  0  0  0  0
M  END


  Mrv0541 08141218052D          

 26 25  0  0  0  0            999 V2000
    4.7759    3.7946    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  0  0  0  0  0  0  0  0  0  0  0
   15.5497    1.3749    0.0000 O   0  0  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
  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  1  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
 13 12  1  0  0  0  0
 16 14  1  0  0  0  0
 16 15  1  0  0  0  0
 17 11  1  0  0  0  0
 18 12  1  0  0  0  0
 19 14  1  0  0  0  0
 20 17  2  0  0  0  0
 23 13  1  0  0  0  0
 24 15  1  0  0  0  0
 25 16  1  0  0  0  0
 25 17  1  0  0  0  0
 26 21  1  0  0  0  0
 26 22  2  0  0  0  0
 26 23  1  0  0  0  0
 26 24  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0031556

> <DATABASE_NAME>
MIME

> <SMILES>
CCCCCCCCCCCC(=O)OC(CO)COP(O)(=O)OCCN

> <INCHI_IDENTIFIER>
InChI=1S/C17H36NO7P/c1-2-3-4-5-6-7-8-9-10-11-17(20)25-16(14-19)15-24-26(21,22)23-13-12-18/h16,19H,2-15,18H2,1H3,(H,21,22)

> <INCHI_KEY>
NPAZKTOOMVQLIH-UHFFFAOYSA-N

> <FORMULA>
C17H36NO7P

> <MOLECULAR_WEIGHT>
397.444

> <EXACT_MASS>
397.222939023

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
43.84991469356734

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2-aminoethoxy)[2-(dodecanoyloxy)-3-hydroxypropoxy]phosphinic acid

> <ALOGPS_LOGP>
1.99

> <JCHEM_LOGP>
1.7515867953270103

> <ALOGPS_LOGS>
-3.42

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.579269652388973

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8688048676175866

> <JCHEM_PKA_STRONGEST_BASIC>
9.999917895738319

> <JCHEM_POLAR_SURFACE_AREA>
128.31

> <JCHEM_REFRACTIVITY>
99.00849999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
19

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.53e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-aminoethoxy(2-(dodecanoyloxy)-3-hydroxypropoxy)phosphinic acid

> <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  N   UNK     0       0.000   0.000   0.000  0.00  0.00           N+0
HETATM   19  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
HETATM   26  P   UNK     0       0.000   0.000   0.000  0.00  0.00           P+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   17                                                       
CONECT   12   13   18                                                       
CONECT   13   12   23                                                       
CONECT   14   16   19                                                       
CONECT   15   16   24                                                       
CONECT   16   14   15   25                                                  
CONECT   17   11   20   25                                                  
CONECT   18   12                                                            
CONECT   19   14                                                            
CONECT   20   17                                                            
CONECT   21   26                                                            
CONECT   22   26                                                            
CONECT   23   13   26                                                       
CONECT   24   15   26                                                       
CONECT   25   16   17                                                       
CONECT   26   21   22   23   24                                             
MASTER        0    0    0    0    0    0    0    0   26    0   50    0
END

Synonyms

Value	Source
(2-Aminoethoxy)[2-(dodecanoyloxy)-3-hydroxypropoxy]phosphinate	Generator

Molecular Formula

C₁₇H₃₆NO₇P

Average Mass

397.444

Monoisotopic Mass

397.222939023

IUPAC Name

(2-aminoethoxy)[2-(dodecanoyloxy)-3-hydroxypropoxy]phosphinic acid

Traditional Name

2-aminoethoxy(2-(dodecanoyloxy)-3-hydroxypropoxy)phosphinic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCC(=O)OC(CO)COP(O)(=O)OCCN

InChI Identifier

InChI=1S/C17H36NO7P/c1-2-3-4-5-6-7-8-9-10-11-17(20)25-16(14-19)15-24-26(21,22)23-13-12-18/h16,19H,2-15,18H2,1H3,(H,21,22)

InChI Key

NPAZKTOOMVQLIH-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.15 g/L	ALOGPS
logP	1.99	ALOGPS
logP	1.75	ChemAxon
logS	-3.4	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	19	ChemAxon
Refractivity	99.01 m³·mol⁻¹	ChemAxon
Polarizability	43.85 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0006-9312000000-56d371f3565c03992ffc	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0006-9300000000-d91990e8ba4ea63fbea9	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0006-9200000000-4df82a29accd9f276d3b	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0002-2916000000-8a2c953b8a1d39dc7697	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-004l-8902000000-fe292329f5b4563d86f1	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9300000000-f578dd08299efd1ce1b2	2015-09-15	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	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

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference
MMDBr0007106	2-Acyl-sn-glycero-3-phosphoethanolamine (N-C12:0)	Dodecanoic acid	Not Available		VMH	30371894

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Proteobacteria	129	Human feces; Human sputum; Human ; Human unknown; Human pleural fluid plaque; Human dental plaque; Human nasal swab; Human stool; Human feces; pleural fluid plaque; bal	Unknown; Metabolic reconstruction
Bacteria	Firmicutes	265	Human feces; Human pleural fluid plaque; Human ; Human stool; Human subgingival plaque; Human saliva	Metabolic reconstruction
Bacteria	Actinobacteria	109	Human feces; Human pleural fluid plaque; Human dental plaque; Human sputum; Human ; Human nasopharyngeal swab; Human mucosa; Human supragingival plaque; Human subgingival plaque; Human saliva	Metabolic reconstruction
Bacteria	Bacteroidetes	20	Human feces; Human	Metabolic reconstruction
Bacteria	Spirochaetes	1	Human feces	Metabolic reconstruction
Archaea	Thaumarchaeota	1		Metabolic reconstruction
Bacteria	Fusobacteria	4	Human feces; Human	Metabolic reconstruction
Bacteria	Planctomycetes	1	Human feces	Metabolic reconstruction

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

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

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

45479565

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-C12:0) (MMDBc0031556)

MOL for #<Metabolite:0x00007feca935b680>

3D MOL for #<Metabolite:0x00007feca935b680>

3D SDF for #<Metabolite:0x00007feca935b680>

3D-SDF for #<Metabolite:0x00007feca935b680>

PDB for #<Metabolite:0x00007feca935b680>

3D PDB for #<Metabolite:0x00007feca935b680>

SMILES for #<Metabolite:0x00007feca935b680>

INCHI for #<Metabolite:0x00007feca935b680>

Structure for #<Metabolite:0x00007feca935b680>

3D Structure for #<Metabolite:0x00007feca935b680>