LTRPC7 inhibitors are chemical compounds designed to specifically target and inhibit the activity of the LTRPC7 channel, also known as TRPM7 (Transient Receptor Potential Melastatin 7). TRPM7 is a unique ion channel that functions as both an ion channel and a kinase, playing a critical role in regulating magnesium and calcium homeostasis within cells. This dual-function protein is involved in various cellular processes such as ion transport, signal transduction, and regulation of cellular growth. LTRPC7 channels are highly sensitive to intracellular levels of magnesium and ADP, and inhibitors of LTRPC7 are developed to block the ion conductance or kinase activity of the channel, thereby affecting its role in maintaining ion balance and cellular signaling.
Chemically, LTRPC7 inhibitors can be diverse, often including small molecules that selectively bind to specific regions of the ion channel or its kinase domain. These inhibitors may function by blocking the pore of the ion channel, preventing the flow of magnesium or calcium ions, or by interfering with the kinase activity, which is essential for its regulatory functions. By inhibiting TRPM7, researchers can study its role in magnesium homeostasis, the regulation of ion transport, and its involvement in cellular signaling pathways. The development and use of LTRPC7 inhibitors are crucial for dissecting the molecular mechanisms underlying TRPM7's dual functions and for understanding how its regulation affects broader physiological processes, including ion channel behavior, cell proliferation, and response to environmental changes. Through these inhibitors, researchers gain valuable insights into the biological roles of TRPM7 in cellular function.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2-APB | 524-95-8 | sc-201487 sc-201487A | 20 mg 100 mg | $28.00 $53.00 | 37 | |
2-APB has been reported to inhibit TRPM7 channels by binding to the channel pore and altering its gating properties. | ||||||
Sodium Orthovanadate | 13721-39-6 | sc-3540 sc-3540B sc-3540A | 5 g 10 g 50 g | $49.00 $57.00 $187.00 | 142 | |
As a general tyrosine phosphatase inhibitor, sodium orthovanadate can prevent the dephosphorylation of regulatory sites on TRPM7, leading to a functional inhibition of channel activity. | ||||||
Spermine | 71-44-3 | sc-212953A sc-212953 sc-212953B sc-212953C | 1 g 5 g 25 g 100 g | $61.00 $196.00 $277.00 $901.00 | 1 | |
While spermine can modulate the activity of ion channels, it can inhibit TRPM7 by plugging the channel pore or by modulating the charge on the cellular membrane. | ||||||
SK&F 96365 | 130495-35-1 | sc-201475 sc-201475B sc-201475A sc-201475C | 5 mg 10 mg 25 mg 50 mg | $103.00 $158.00 $397.00 $656.00 | 2 | |
SKF-96365 inhibits TRPM7 channels by interfering with the channel's conductance mechanism, likely by acting at or near the channel pore. | ||||||
Amiloride • HCl | 2016-88-8 | sc-3578 sc-3578A | 25 mg 100 mg | $22.00 $57.00 | 6 | |
Amiloride is known to inhibit a range of ion channels and transporters, and it can reduce TRPM7 channel activity, possibly by interacting with the channel's pore-forming region. | ||||||
Econazole | 27220-47-9 | sc-279013 | 5 g | $240.00 | ||
Econazole, primarily an antifungal agent, can inhibit TRPM7 channels, likely due to its interaction with the lipid environment of the channel or the channel protein itself. | ||||||
Gadolinium | 7440-54-2 | sc-250038 | 10 g | $89.00 | ||
Gadolinium ions are known to block various cation channels, including TRPM7, by obstructing the channel pore. | ||||||