Page last updated: 2024-12-07

1-o-myristoyl-2-acetyl-glycerol

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

1-O-myristoyl-2-acetyl-glycerol (MAG) is a **monoacylglycerol** (MAG), a type of lipid that consists of a glycerol molecule with one fatty acid chain attached.

**Structure:**

* **Myristoyl:** A saturated fatty acid with 14 carbon atoms (C14:0). This is attached to the glycerol molecule at the sn-1 position.
* **Acetyl:** A short chain fatty acid with 2 carbon atoms (C2:0). This is attached to the glycerol molecule at the sn-2 position.

**Importance in Research:**

MAG, including 1-O-myristoyl-2-acetyl-glycerol, is of interest in various research areas due to its potential roles in:

1. **Cellular Signaling:**
* **Endocannabinoid System:** MAGs can act as endogenous ligands for cannabinoid receptors, specifically CB1 and CB2, which are involved in various physiological processes like pain perception, appetite regulation, and immune responses.
* **Other Signaling Pathways:** MAGs have been shown to activate other signaling pathways, including the protein kinase C (PKC) pathway, which is important for cell growth, differentiation, and survival.

2. **Metabolic Processes:**
* **Lipogenesis:** MAGs are intermediates in the synthesis of triglycerides, the primary form of fat storage in the body.
* **Lipolysis:** MAGs can be hydrolyzed to produce glycerol and free fatty acids, contributing to energy metabolism.
* **Intestinal Absorption:** MAGs are important for the absorption of dietary fats in the intestines.

3. **Therapeutic Potential:**
* **Neurological Disorders:** MAGs are being investigated as potential therapeutic agents for neurological disorders like Alzheimer's disease and Parkinson's disease, as they can modulate neuronal activity and protect against neurotoxicity.
* **Metabolic Diseases:** MAGs might have potential benefits for metabolic diseases like obesity and type 2 diabetes by influencing lipid metabolism and insulin sensitivity.

**Current Research:**

Researchers are actively investigating the following aspects of MAGs:

* **Synthesis and Metabolism:** Understanding how MAGs are synthesized and metabolized in the body is crucial for developing therapeutic strategies.
* **Biological Activity:** Identifying specific pathways and receptors involved in MAG signaling will provide insights into its physiological and therapeutic roles.
* **Drug Development:** Developing novel MAG-based drugs that target specific pathways could have promising applications in various disease areas.

Overall, 1-O-myristoyl-2-acetyl-glycerol and other MAGs hold significant potential for research, particularly in the fields of endocannabinoid signaling, lipid metabolism, and drug development. Continued research will provide a deeper understanding of their roles in the body and their potential for therapeutic applications.

Cross-References

ID SourceID
PubMed CID124835
CHEMBL ID186395
MeSH IDM0130575

Synonyms (12)

Synonym
1-mag
glycerol 1-myristate 2-acetate
(2-acetyloxy-3-hydroxypropyl) tetradecanoate
92758-88-8
CHEMBL186395
1-o-myristoyl-2-acetyl-glycerol
tetradecanoic acid, 2-(acetyloxy)-3-hydroxypropyl ester, (+-)-
100307-94-6
DTXSID20276280
2-(acetyloxy)-3-hydroxypropyl tetradecanoate
DTXSID40918973
1-tetradecanoyl-2-acetyl-glycerole
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID239686Displacement of [20-3H]-phorbol 12,13-dibutyrate (PDBU) from recombinant Protein kinase C alpha (C1a/C1b domain) in presence of phosphatidyl serine 2004Journal of medicinal chemistry, Jul-29, Volume: 47, Issue:16
Macrocyclic diacylglycerol-bis-lactones as conformationally constrained analogues of diacylglycerol-lactones. Interactions with protein kinase C.
AID237417Partition coefficient (logP)2004Journal of medicinal chemistry, Jul-29, Volume: 47, Issue:16
Macrocyclic diacylglycerol-bis-lactones as conformationally constrained analogues of diacylglycerol-lactones. Interactions with protein kinase C.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (50.00)18.7374
1990's0 (0.00)18.2507
2000's1 (16.67)29.6817
2010's2 (33.33)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: 12.64

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 Index12.64 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.59 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.64)

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]