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.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
佛司可林能激活腺苷酸环化酶,从而通过 cAMP 介导的信号途径间接影响 LPCAT2 的表达。 | ||||||
Lipase Inhibitor, THL | 96829-58-2 | sc-203108 | 50 mg | $51.00 | 7 | |
脂肪酶抑制剂可间接影响脂质代谢途径,包括 LPCAT(溶血磷脂酰胆碱酰基转移酶)的作用。 | ||||||
GW4869 | 6823-69-4 | sc-218578 sc-218578A | 5 mg 25 mg | $199.00 $599.00 | 24 | |
GW4869是一种常用的药理抑制剂,用于阻断外泌体释放。它抑制中性鞘氨醇酶2(nSMase2)的活性,间接影响LPCAT1介导的脂质重塑。 | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $65.00 $267.00 | 257 | |
SP600125 是一种 JNK 抑制剂,可能会通过改变应激反应信号来影响 LPCAT2 的表达。 | ||||||
GW 5074 | 220904-83-6 | sc-200639 sc-200639A | 5 mg 25 mg | $106.00 $417.00 | 10 | |
GW5074是一种蛋白激酶CK的选择性抑制剂。据报道,在某些实验条件下,它可抑制LPCAT1活性,但抑制的具体机制尚不完全清楚。 | ||||||
Triacsin C Solution in DMSO | 76896-80-5 | sc-200574 sc-200574A | 100 µg 1 mg | $149.00 $826.00 | 14 | |
它是长链酰基-CoA 合成酶的抑制剂,可间接影响 LPCAT(溶血磷脂酰胆碱酰基转移酶)的底物供应。 | ||||||
NDGA (Nordihydroguaiaretic acid) | 500-38-9 | sc-200487 sc-200487A sc-200487B | 1 g 5 g 25 g | $107.00 $376.00 $2147.00 | 3 | |
NDGA 是一种存在于杂酚油灌木中的天然化合物。据报道,它能抑制 LPCAT1 的活性,导致某些细胞的脂质代谢发生改变。 | ||||||
D609 | 83373-60-8 | sc-201403 sc-201403A | 5 mg 25 mg | $185.00 $564.00 | 7 | |
虽然它主要针对磷脂酰胆碱特异性磷脂酶 C 和 D,但也可能对 LPCAT 产生间接影响。 | ||||||
Cerulenin (synthetic) | 17397-89-6 | sc-200827 sc-200827A sc-200827B | 5 mg 10 mg 50 mg | $158.00 $306.00 $1186.00 | 9 | |
脂肪酸合酶的抑制剂,可通过改变脂肪酸代谢间接影响 LPCAT。 |