MiMeDB: Showing metabocard for 2-tetradec-7-enoyl-sn-glycerol 3-phosphate (MMDBc0031580)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-18 01:40:03 UTC

Update Date

2022-08-31 18:21:55 UTC

Metabolite ID

MMDBc0031580

Metabolite Identification

Common Name

2-tetradec-7-enoyl-sn-glycerol 3-phosphate

Description

2-tetradec-7-enoyl-sn-glycerol 3-phosphate belongs to the class of Fatty Acid Esters. These are carboxylic ester derivatives of a fatty acid. (inferred from compound structure)

Structure

MOL SDF PDB SMILES InChI


  Mrv0541 10101207442D          

 25 24  0  0  0  0            999 V2000
   -2.8579    5.9368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    5.5243    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5559    4.8099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7309    6.2388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.1118    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.8743    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    5.5243    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    4.2868    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.8743    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    5.1118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    5.5243    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.3493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    6.7618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    7.5868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    7.9993    0.0000 C   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
  2  4  2  0  0  0  0
  2  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
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0031580

> <DATABASE_NAME>
MIME

> <SMILES>
CCCCCC\C=C/CCCCCC(=O)OC(CO)COP(O)(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H33O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-17(19)24-16(14-18)15-23-25(20,21)22/h7-8,16,18H,2-6,9-15H2,1H3,(H2,20,21,22)/b8-7-

> <INCHI_KEY>
KKNDQWWVDATMLV-FPLPWBNLSA-N

> <FORMULA>
C17H33O7P

> <MOLECULAR_WEIGHT>
380.4135

> <EXACT_MASS>
380.196389922

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
41.17889058088156

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
{3-hydroxy-2-[(7Z)-tetradec-7-enoyloxy]propoxy}phosphonic acid

> <ALOGPS_LOGP>
3.15

> <JCHEM_LOGP>
3.707414861666668

> <ALOGPS_LOGS>
-3.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.345670795497974

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.3198427043855405

> <JCHEM_PKA_STRONGEST_BASIC>
-2.983758075742787

> <JCHEM_POLAR_SURFACE_AREA>
113.29000000000002

> <JCHEM_REFRACTIVITY>
96.895

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.03e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-hydroxy-2-[(7Z)-tetradec-7-enoyloxy]propoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-OCT-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-OCT-12         0                                  
HETATM    1  O   UNK     0      -5.335  11.082   0.000  0.00  0.00           O+0
HETATM    2  P   UNK     0      -4.001  10.312   0.000  0.00  0.00           P+0
HETATM    3  O   UNK     0      -4.771   8.978   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -3.231  11.646   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      -2.667   9.542   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.334  10.312   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.000   9.542   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.000   8.002   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.334   7.232   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       1.334  10.312   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.667   9.542   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.667   8.002   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.001  10.312   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   9.542   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668  10.312   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002   9.542   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002   8.002   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336   7.232   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.669   8.002   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.669   9.542   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.336  10.312   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.336  11.852   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.002  12.622   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.002  14.162   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.668  14.932   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   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                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

Synonyms

Value	Source
2-Tetradec-7-enoyl-sn-glycerol 3-phosphoric acid	Generator
{3-hydroxy-2-[(7Z)-tetradec-7-enoyloxy]propoxy}phosphonate	Generator

Molecular Formula

C₁₇H₃₃O₇P

Average Mass

380.4135

Monoisotopic Mass

380.196389922

IUPAC Name

{3-hydroxy-2-[(7Z)-tetradec-7-enoyloxy]propoxy}phosphonic acid

Traditional Name

3-hydroxy-2-[(7Z)-tetradec-7-enoyloxy]propoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

CCCCCC\C=C/CCCCCC(=O)OC(CO)COP(O)(O)=O

InChI Identifier

InChI=1S/C17H33O7P/c1-2-3-4-5-6-7-8-9-10-11-12-13-17(19)24-16(14-18)15-23-25(20,21)22/h7-8,16,18H,2-6,9-15H2,1H3,(H2,20,21,22)/b8-7-

InChI Key

KKNDQWWVDATMLV-FPLPWBNLSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-acylglycerol-3-phosphates. These are lysophosphatidic acids where the glycerol is esterified with a fatty acid at O-2 position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphates

Direct Parent

2-acylglycerol-3-phosphates

Alternative Parents

Substituents

2-acylglycerol-3-phosphate
Monoalkyl phosphate
Fatty acid ester
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen 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	0.04 g/L	ALOGPS
logP	3.15	ALOGPS
logP	3.71	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	1.32	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	113.29 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	96.9 m³·mol⁻¹	ChemAxon
Polarizability	41.18 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_2_2) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-053r-3898000000-80c1fc0ef487994a2e0e	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0a4i-6951000000-c3ed1e94445928d11a62	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0ar0-9820000000-70d6b4a26a4367696508	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-004i-8978000000-70c5044d0fb46130478c	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-004i-9110000000-3aa621695bdec99d9293	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9000000000-c382b164b3c2c2ec7271	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

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference
MMDBr0007101	2-tetradec-7-enoyl-sn-glycerol 3-phosphate	Glycerol 3-phosphate	Not Available	Lysophospholipase L2 (2-acylglycerophosphotidate, n-C14:1)	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

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-tetradec-7-enoyl-sn-glycerol 3-phosphate (MMDBc0031580)

MOL for #<Metabolite:0x000055d24b2789b8>

3D MOL for #<Metabolite:0x000055d24b2789b8>

3D SDF for #<Metabolite:0x000055d24b2789b8>

3D-SDF for #<Metabolite:0x000055d24b2789b8>

PDB for #<Metabolite:0x000055d24b2789b8>

3D PDB for #<Metabolite:0x000055d24b2789b8>

SMILES for #<Metabolite:0x000055d24b2789b8>

INCHI for #<Metabolite:0x000055d24b2789b8>

Structure for #<Metabolite:0x000055d24b2789b8>

3D Structure for #<Metabolite:0x000055d24b2789b8>