Date published: 2026-1-9

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LPL Inhibitors

Lipoprotein lipase (LPL) inhibitors constitute a distinct chemical class designed to selectively target and modulate the activity of lipoprotein lipase, an enzyme crucial for lipid metabolism. Lipoprotein lipase plays a pivotal role in breaking down triglycerides carried by circulating lipoproteins, thus facilitating the release of fatty acids for cellular uptake and energy production. These inhibitors are crafted to interact with specific sites on the lipoprotein lipase enzyme, influencing its catalytic function and, consequently, impacting lipid processing and distribution within the body. Lipoprotein lipase is primarily found at the surface of endothelial cells lining blood vessels, particularly in tissues that require a constant supply of fatty acids, such as adipose tissue and skeletal muscle. By regulating the breakdown of triglycerides in circulating lipoproteins, LPL inhibitors can influence overall lipid metabolism, cellular energy balance, and lipid storage. Investigating the effects of LPL inhibitors provides insights into the intricate molecular mechanisms governing lipid utilization, storage, and transport. Understanding these processes can contribute to a broader comprehension of metabolic regulation and its implications for overall health. This exploration aids in advancing our knowledge of lipid-related diseases, cellular energetics, and the broader context of lipid metabolism in maintaining cellular homeostasis.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Lipase Inhibitor, THL

96829-58-2sc-203108
50 mg
$52.00
7
(1)

A reversible inhibitor of pancreatic lipase, which indirectly affects LPL. By inhibiting pancreatic lipase, orlistat reduces the digestion and absorption of dietary fats. This leads to a decrease in the availability of fatty acids, potentially affecting LPL-mediated lipoprotein metabolism and utilization of triglycerides.

GSK 264220A

685506-42-7sc-295026
sc-295026A
10 mg
50 mg
$181.00
$749.00
(0)

GSK 264220A is notable for its reactivity as an acid halide, particularly in acylation reactions where it readily forms stable intermediates. Its electrophilic nature facilitates rapid nucleophilic attack, leading to efficient formation of esters and amides. The compound's unique steric configuration influences its interaction with nucleophiles, resulting in distinct reaction kinetics. Additionally, GSK 264220A exhibits selective solubility, enhancing its compatibility with diverse reaction media.

Citilistat

282526-98-1sc-358100
sc-358100A
250 mg
1 g
$47.00
$104.00
(0)

Similar to orlistat, cetilistat is a pancreatic lipase inhibitor that may impact LPL activity indirectly. Its mechanism involves reducing the absorption of dietary fats, potentially leading to changes in lipoprotein metabolism and triglyceride utilization through LPL-mediated processes.

Bezafibrate

41859-67-0sc-204650B
sc-204650
sc-204650A
sc-204650C
500 mg
1 g
5 g
10 g
$31.00
$46.00
$122.00
$204.00
5
(1)

Bezabrate is a fibrate compound used for dyslipidemia. It may impact LPL activity indirectly by altering gene expression related to lipid metabolism. It can increase LPL synthesis and enhance lipoprotein clearance, leading to improved triglyceride and cholesterol levels.