LPCAT1 Inhibitors are a specialized class of chemical compounds designed to target and inhibit the activity of Lysophosphatidylcholine Acyltransferase 1 (LPCAT1), an enzyme that plays a critical role in phospholipid metabolism. LPCAT1 is responsible for catalyzing the conversion of lysophosphatidylcholine (LPC) into phosphatidylcholine (PC) by incorporating a fatty acyl group into the LPC molecule. This enzyme is essential in maintaining the balance of phospholipids within cell membranes, which are crucial for membrane structure, fluidity, and function. LPCAT1 is particularly important in tissues with high membrane turnover or those requiring rapid remodeling of lipid components, such as the lungs, where it contributes to the production of surfactant, a substance that reduces surface tension and prevents lung collapse.
Inhibition of LPCAT1 offers researchers a valuable tool for studying the broader implications of phospholipid metabolism and its impact on cellular processes. By inhibiting LPCAT1, scientists can explore how disruptions in phospholipid biosynthesis affect membrane dynamics, cellular signaling pathways, and the overall homeostasis of lipid composition within cells. LPCAT1 inhibitors are particularly useful in research focused on understanding how alterations in membrane lipid composition can influence cell behavior, such as changes in membrane permeability, signaling receptor localization, and interactions with extracellular molecules. Additionally, these inhibitors allow for the investigation of LPCAT1's role in specific biological processes, such as lipid droplet formation, energy storage, and lipid signaling pathways. The availability of LPCAT1 inhibitors enables detailed exploration of these processes, contributing to a deeper understanding of lipid metabolism and its significance in various physiological contexts.
Items 1 to 10 of 19 total
展示:
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
---|---|---|---|---|---|---|
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
西罗莫司可抑制 mTOR 信号转导,这可能会下调 LPCAT2 的表达,从而对脂质代谢产生更广泛的影响。 | ||||||
Avasimibe | 166518-60-1 | sc-364315 sc-364315A sc-364315B sc-364315C | 10 mg 50 mg 500 mg 1 g | $107.00 $413.00 $2040.00 $3060.00 | 1 | |
它最初被开发为胆固醇代谢的ACAT抑制剂,现已证明会影响磷脂代谢,并可能影响LPCAT(溶血磷脂酰胆碱酰基转移酶)的活性。 | ||||||
Quinacrine, Dihydrochloride | 69-05-6 | sc-204222 sc-204222B sc-204222A sc-204222C sc-204222D | 100 mg 1 g 5 g 200 g 300 g | $45.00 $56.00 $85.00 $3193.00 $4726.00 | 4 | |
喹吖啶是一种抗疟疾药物,已被发现可抑制 LPCAT1 的活性。它能阻断 LPCAT1 的酰基转移酶功能,导致 PC 合成减少。 | ||||||
BEZ235 | 915019-65-7 | sc-364429 | 50 mg | $207.00 | 8 | |
Dactolisib 是一种 PI3K/mTOR 双重抑制剂,可能会通过改变脂质合成途径来影响 LPCAT2 的表达。 | ||||||
Probenecid | 57-66-9 | sc-202773 sc-202773A sc-202773B sc-202773C | 1 g 5 g 25 g 100 g | $27.00 $38.00 $98.00 $272.00 | 28 | |
据报道,丙磺舒可抑制 LPCAT1,导致脂质代谢改变。 | ||||||
Sorafenib | 284461-73-0 | sc-220125 sc-220125A sc-220125B | 5 mg 50 mg 500 mg | $56.00 $260.00 $416.00 | 129 | |
索拉非尼靶向多种激酶,可能会通过调节信号转导途径影响 LPCAT2 的表达。 | ||||||
Fenofibrate | 49562-28-9 | sc-204751 | 5 g | $40.00 | 9 | |
非诺贝特主要是一种 PPARα 激动剂,用于治疗高脂血症,但它也能间接影响脂质代谢途径,可能会影响 LPCAT(溶血磷脂酰胆碱酰基转移酶)的活性。 | ||||||
Rosiglitazone | 122320-73-4 | sc-202795 sc-202795A sc-202795C sc-202795D sc-202795B | 25 mg 100 mg 500 mg 1 g 5 g | $118.00 $320.00 $622.00 $928.00 $1234.00 | 38 | |
罗格列酮是一种 PPARγ 激动剂,可能会通过影响脂质代谢基因来下调 LPCAT2 的表达。 | ||||||
Tunicamycin | 11089-65-9 | sc-3506A sc-3506 | 5 mg 10 mg | $169.00 $299.00 | 66 | |
Tunicamycin 可抑制 N-连接的糖基化,通过诱导 ER 应激和未折叠蛋白反应来影响 LPCAT2 的表达。 | ||||||
Miltefosine | 58066-85-6 | sc-203135 | 50 mg | $79.00 | 8 | |
一种影响磷脂代谢的烷基磷脂酰胆碱药物,可间接影响 LPCAT(溶血磷脂酰胆碱酰基转移酶)的功能。 |