Page last updated: 2024-12-06

1-myristylpicolinium

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

Description

1-myristylpicolinium, also known as **myristylpyridinium chloride**, is a **cationic surfactant** that is a long-chain alkyl derivative of pyridine. It is commonly used in research for several reasons:

**1. Antimicrobial Activity:**

* 1-myristylpicolinium is a **potent antimicrobial agent** effective against a broad spectrum of bacteria, fungi, and viruses.
* Its mechanism of action involves disrupting cell membranes, leading to cell lysis and death.
* This makes it a valuable tool for studying antimicrobial mechanisms and developing new antimicrobial therapies.

**2. Biofilm Inhibition:**

* Biofilms are communities of bacteria encased in a protective matrix, making them resistant to antibiotics.
* 1-myristylpicolinium has shown promising results in **inhibiting biofilm formation** by disrupting the matrix and affecting bacterial communication.
* This property is important for research in areas like infection control, wound healing, and medical device design.

**3. Gene Delivery:**

* As a cationic surfactant, 1-myristylpicolinium can form complexes with negatively charged DNA or RNA molecules.
* This ability makes it a potential **carrier for gene delivery**, offering a way to introduce genetic material into cells for therapeutic or research purposes.

**4. Membrane Interaction Studies:**

* Due to its amphiphilic nature, 1-myristylpicolinium interacts with cell membranes.
* This makes it a useful tool for **studying membrane structure, dynamics, and permeability**.
* Researchers can use it to investigate the effects of different compounds or environmental factors on membrane integrity.

**5. Nanomaterials Synthesis:**

* 1-myristylpicolinium can be used as a **template for the synthesis of nanomaterials**, such as nanoparticles and nanotubes.
* This is because its long alkyl chain and positively charged head can interact with specific materials and control their assembly.

**Importance in Research:**

* 1-myristylpicolinium's diverse properties make it a versatile tool for researchers in various fields, including **microbiology, biomedicine, materials science, and nanotechnology**.
* Its potential applications range from developing new antimicrobial therapies to designing advanced drug delivery systems.
* Ongoing research continues to explore the full potential of this compound, leading to exciting discoveries and advancements in different areas of science.

**Note:** Although 1-myristylpicolinium shows promise in research, it's important to note that its use in medical and therapeutic applications requires careful consideration of its potential toxicity and side effects.

1-myristylpicolinium: suppresses cartilage & synovial membrane glycosaminoglycan sythesis; RN refers to chloride [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID17672
CHEMBL ID1393904
SCHEMBL ID3477808
MeSH IDM0154491

Synonyms (16)

Synonym
NCGC00181085-01
1-myristylpicolinium
miripirium ion
myristyl-gamma-picolinium
CHEMBL1393904
miripirium cation
myristyl-.gamma.-picolinium
pyridinium, 4-methyl-1-tetradecyl-
7631-49-4
miripirium
3rok0lrz8l ,
unii-3rok0lrz8l
SCHEMBL3477808
DTXSID9048275
pyridinium,4-methyl-1-tetradecyl-
Q27257947
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (9)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
phosphopantetheinyl transferaseBacillus subtilisPotency56.23410.141337.9142100.0000AID1490
USP1 protein, partialHomo sapiens (human)Potency56.23410.031637.5844354.8130AID504865
euchromatic histone-lysine N-methyltransferase 2Homo sapiens (human)Potency3.16230.035520.977089.1251AID504332
vitamin D3 receptor isoform VDRAHomo sapiens (human)Potency70.79460.354828.065989.1251AID504847
huntingtin isoform 2Homo sapiens (human)Potency22.38720.000618.41981,122.0200AID1688
nuclear receptor ROR-gamma isoform 1Mus musculus (house mouse)Potency8.28520.00798.23321,122.0200AID2546; AID2551
gemininHomo sapiens (human)Potency16.78890.004611.374133.4983AID624297
peripheral myelin protein 22Rattus norvegicus (Norway rat)Potency11.24750.005612.367736.1254AID624032; AID624044
ATP-dependent phosphofructokinaseTrypanosoma brucei brucei TREU927Potency31.62280.060110.745337.9330AID492961
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID504749qHTS profiling for inhibitors of Plasmodium falciparum proliferation2011Science (New York, N.Y.), Aug-05, Volume: 333, Issue:6043
Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (25.00)18.7374
1990's4 (50.00)18.2507
2000's1 (12.50)29.6817
2010's1 (12.50)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies2 (25.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (75.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]