MiMeDB: Showing metabocard for LysoPC(0:0/20:0) (MMDBc0060132)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2023-02-02 20:27:51 UTC

Update Date

2023-02-02 20:27:51 UTC

Metabolite ID

MMDBc0060132

Metabolite Identification

Common Name

LysoPC(0:0/20:0)

Description

(2-{[(2R)-3-hydroxy-2-(icosanoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium belongs to the class of organic compounds known as 2-acyl-sn-glycero-3-phosphocholines. These are glycerophosphocholines in which the glycerol is esterified with a fatty acid at O-2 position, and linked at position 3 to a phosphocholine. Based on a literature review very few articles have been published on (2-{[(2R)-3-hydroxy-2-(icosanoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Not Available

Molecular Formula

C₂₈H₅₈NO₇P

Average Mass

551.746

Monoisotopic Mass

551.39509021

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

Not Available

InChI Identifier

Not Available

InChI Key

WQBSSUPHAAAVSW-HHHXNRCGSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-acyl-sn-glycero-3-phosphocholines. These are glycerophosphocholines in which the glycerol is esterified with a fatty acid at O-2 position, and linked at position 3 to a phosphocholine.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Glycerophospholipids

Sub Class

Glycerophosphocholines

Direct Parent

2-acyl-sn-glycero-3-phosphocholines

Alternative Parents

Substituents

2-acyl-sn-glycero-3-phosphocholine
Phosphocholine
Dialkyl phosphate
Fatty acid ester
Fatty acyl
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Tetraalkylammonium salt
Quaternary ammonium salt
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organic salt
Primary alcohol
Organooxygen compound
Organonitrogen compound
Carbonyl group
Amine
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Not Available

Predicted Properties

Not Available

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

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
MMDBr0036840	PC(10:0/20:0)	Decanoate (N-C10:0)	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036818	PC(12:0/20:0)	Dodecanoate (N-C12:0)	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0037005	PC(14:1(11Z)/20:0)	(11Z)-Tetradecenoic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036742	PC(14:1(9Z)/20:0)	Myristoleic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036993	PC(15:1(11Z)/20:0)	(11Z)-Pentadecenoic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0037019	PC(15:1(9Z)/20:0)	(9Z)-pentadec-9-enoic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036802	PC(16:1(11Z)/20:0)	11-hexadecenoic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0037041	PC(16:1(9Z)/20:0)	(9Z)-hexadecenoic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036716	PC(18:3(6Z,9Z,12Z)/20:0)	gamma-Linolenic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036674	PC(18:3(9Z,12Z,15Z)/20:0)	alpha-Linolenic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036952	PC(18:4(6Z,9Z,12Z,15Z)/20:0)	Stearidonic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0037059	PC(20:2(11Z,14Z)/20:0)	(11Z,14Z)-eicosadienoic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036981	PC(20:3(5Z,8Z,11Z)/20:0)	5,8,11-Eicosatrienoic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036774	PC(20:3(8Z,11Z,14Z)/20:0)	Dihomo-gamma-linolenic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036654	PC(20:4(5Z,8Z,11Z,14Z)/20:0)	Arachidonic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036939	PC(20:4(8Z,11Z,14Z,17Z)/20:0)	Cis-8,11,14,17-Eicosatetraenoic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036721	PC(20:5(5Z,8Z,11Z,14Z,17Z)/20:0)	Eicosapentaenoic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036930	PC(22:1(13Z)/20:0)	Erucic acid	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036790	PC(22:2(13Z,16Z)/20:0)	Docosadienoate (22:2n6)	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880
MMDBr0036796	PC(22:4(7Z,10Z,13Z,16Z)/20:0)	(7Z,10Z,13Z,16Z)-docosatetraenoate	cGAMP-activated phospholipase	Hydrolysis	RHEA	34755880

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

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

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

21403163

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

Showing metabocard for LysoPC(0:0/20:0) (MMDBc0060132)

MOL for #<Metabolite:0x00007fd0f80325c0>

3D MOL for #<Metabolite:0x00007fd0f80325c0>

3D SDF for #<Metabolite:0x00007fd0f80325c0>

3D-SDF for #<Metabolite:0x00007fd0f80325c0>

PDB for #<Metabolite:0x00007fd0f80325c0>

3D PDB for #<Metabolite:0x00007fd0f80325c0>

SMILES for #<Metabolite:0x00007fd0f80325c0>

INCHI for #<Metabolite:0x00007fd0f80325c0>

Structure for #<Metabolite:0x00007fd0f80325c0>

3D Structure for #<Metabolite:0x00007fd0f80325c0>