LPAAT-θ inhibitors belong to a class of chemical compounds developed to target and inhibit the activity of Lysophosphatidic acid acyltransferase theta (LPAAT-θ). LPAAT-θ is an enzyme involved in the metabolism of lipids and plays a critical role in lipid biosynthesis pathways, particularly in the conversion of lysophosphatidic acid (LPA) into phosphatidic acid (PA). This enzymatic reaction is a key step in the biosynthesis of glycerophospholipids and triglycerides, which are essential components of cell membranes and storage lipids, respectively. LPAAT-θ inhibitors are valuable tools for researchers studying lipid metabolism, membrane biogenesis, and the regulation of cellular lipid homeostasis.
Typically composed of small molecules or chemical compounds, LPAAT-θ inhibitors are specifically designed to interfere with the activity or interactions of LPAAT-θ within cellular pathways. By inhibiting LPAAT-θ, these compounds can potentially disrupt the conversion of LPA to PA, leading to alterations in lipid biosynthesis and metabolism. Researchers use LPAAT-θ inhibitors in laboratory settings to manipulate the activity of this enzyme and study its roles in various biological contexts, including those related to lipid metabolism, cell membrane composition, and energy storage. These inhibitors provide valuable insights into the molecular mechanisms by which LPAAT-θ contributes to lipid biosynthesis and cellular lipid homeostasis, enhancing our understanding of the complex processes governing lipid metabolism in cells. While LPAAT-θ inhibitors may have broader implications, their primary purpose is to assist scientists in deciphering the intricacies of LPAAT-θ-mediated lipid metabolic processes.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Inhibits the mTOR pathway, which could reduce protein synthesis and potentially decrease LPAAT-θ expression. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
A PI3K inhibitor, which could downregulate various biosynthetic processes, potentially including LPAAT-θ expression. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Another PI3K inhibitor, it could also disrupt protein synthesis pathways, potentially affecting LPAAT-θ expression levels. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
A natural compound known to modulate a variety of cellular processes, which might include downregulation of LPAAT-θ expression. | ||||||
D,L-Sulforaphane | 4478-93-7 | sc-207495A sc-207495B sc-207495C sc-207495 sc-207495E sc-207495D | 5 mg 10 mg 25 mg 1 g 10 g 250 mg | $150.00 $286.00 $479.00 $1299.00 $8299.00 $915.00 | 22 | |
This compound can influence gene expression through Nrf2 signaling, which may affect proteins like LPAAT-θ. | ||||||
Tetracycline | 60-54-8 | sc-205858 sc-205858A sc-205858B sc-205858C sc-205858D | 10 g 25 g 100 g 500 g 1 kg | $62.00 $92.00 $265.00 $409.00 $622.00 | 6 | |
A compund known to inhibit mitochondrial protein synthesis, which could non-specifically affect LPAAT-θ expression. | ||||||
Chloramphenicol | 56-75-7 | sc-3594 | 25 g | $53.00 | 10 | |
Also a compound that inhibits bacterial protein synthesis, with possible off-target effects on mitochondrial biogenesis and protein expression. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Modulates gene expression via nuclear receptors, which could potentially influence LPAAT-θ expression. | ||||||
Spironolactone | 52-01-7 | sc-204294 | 50 mg | $107.00 | 3 | |
An aldosterone antagonist with potential to alter gene expression profiles, which might include proteins like LPAAT-θ. | ||||||
3′-Azido-3′-deoxythymidine | 30516-87-1 | sc-203319 | 10 mg | $60.00 | 2 | |
A nucleoside analog reverse transcriptase inhibitor, known to have off-target effects on mitochondrial DNA replication and protein expression. | ||||||