Page last updated: 2024-12-08

1,2-didodecanoyl-glycero-3-phosphocholine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

1,2-didodecanoyl-glycero-3-phosphocholine, also known as **di-lauroyl-phosphatidylcholine (DLPC)**, is a synthetic phospholipid. Here's a breakdown of its structure and importance in research:

**Structure:**

* **Phospholipid:** DLPC is a type of lipid that contains a phosphate group, a glycerol backbone, and two fatty acid chains.
* **Fatty Acid Chains:** DLPC has two lauric acid chains (12 carbons each).
* **Phosphocholine Headgroup:** It has a choline (CH3)3N+CH2CH2OH group attached to the phosphate.

**Importance in Research:**

DLPC is used in various scientific fields, primarily due to its **physical properties** and its role as a **model system:**

1. **Model Membrane System:**

* **Lipid Bilayer Formation:** DLPC readily forms stable, well-defined lipid bilayers in aqueous solutions. These bilayers mimic the structure of biological cell membranes, making DLPC crucial for studying:
* **Membrane Dynamics:** How membranes move, interact, and change shape.
* **Protein-Membrane Interactions:** How proteins associate with, integrate into, and function within cell membranes.
* **Drug Delivery:** How drugs interact with and penetrate membranes.
* **Liposome Formation:** DLPC can form liposomes, which are spherical vesicles made of lipid bilayers. Liposomes are used as drug carriers and in research on drug delivery, gene therapy, and other biomedical applications.

2. **Physical Properties:**

* **Phase Transitions:** DLPC undergoes well-defined phase transitions, making it useful for studying the physical properties of lipid membranes. This includes studying how temperature, pressure, and other factors affect membrane fluidity and organization.
* **Surface Tension:** DLPC can be used to study surface tension and interfacial properties, which are important in fields like materials science and colloid chemistry.

3. **Biophysical Studies:**

* **Spectroscopy:** DLPC is often used in spectroscopic studies like fluorescence spectroscopy, circular dichroism, and nuclear magnetic resonance (NMR) to probe the structure and dynamics of membranes.
* **Microscopy:** DLPC is used in microscopy techniques, such as atomic force microscopy (AFM) and electron microscopy, to visualize the structure of membranes and membrane-associated proteins.

**Overall, DLPC serves as a valuable tool for researchers in various fields, including:**

* **Biochemistry**
* **Biophysics**
* **Cell Biology**
* **Pharmacology**
* **Material Science**

It provides a simplified yet highly relevant model system for studying the complex behavior of biological membranes and their interactions with other molecules.

Cross-References

ID SourceID
PubMed CID173953
CHEBI ID60725
SCHEMBL ID23435337
MeSH IDM0153523

Synonyms (17)

Synonym
c12:0 pg
1,2-dilauroylphosphatidylglycerol
CHEBI:60725
c12:0 phosphatidylglycerol
didodecanoyl phosphatidylglycerol
dilauroylphosphatidylglycerol
dic(12)pg
1,2-didodecanoyl-sn-glycero-3-phospho-(1'-rac-glycerol)
63644-55-3
1,2-didodecanoyl-glycero-3-phosphocholine
dodecanoic acid, 1-((((2,3-dihydroxypropoxy)hydroxyphosphinyl)oxy)methyl)-1,2-ethanediyl ester
Q27128564
3-{[(2,3-dihydroxypropoxy)(hydroxy)phosphoryl]oxy}-2-(dodecanoyloxy)propyl dodecanoate
DTXSID70979870
SCHEMBL23435337
PD047001
pg 12:0_12:0
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
phosphatidylglycerolA glycerophosphoglycerol that is glycerol in which the hydrogen of one of the primary hydroxy groups has been replaced by a phosphatidyl group.
dodecanoate esterAny fatty acid ester in which the carboxylic acid component is lauric acid.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (33.33)18.7374
1990's1 (16.67)18.2507
2000's0 (0.00)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.52

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.52 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.46 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.52)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]