COPT2 inhibitors, also known as copper transport protein 2 inhibitors, represent a diverse class of chemical compounds designed to modulate the activity of the copper transporter protein COPT2. COPT2 is a crucial membrane protein found in various organisms, including bacteria and eukaryotes, that plays a pivotal role in copper homeostasis by facilitating the uptake of copper ions from the extracellular environment into cells. Inhibitors of COPT2 are primarily researched and developed for their applications in basic scientific investigations and studies related to copper metabolism. These inhibitors exert their effects by interfering with the normal functioning of COPT2, leading to disruptions in copper transport across biological membranes.
The mechanisms of COPT2 inhibitors can vary, but they often involve the binding of these compounds to COPT2's active site or copper-binding domains, thereby impeding the transporter's ability to facilitate copper uptake. This disruption in copper transport can have profound implications for various biological processes since copper serves as an essential cofactor for numerous enzymes involved in critical cellular functions, including respiration, oxidative stress defense, and neurotransmitter synthesis. By inhibiting COPT2, these compounds can lead to copper deficiency within cells, affecting these fundamental processes. Researchers utilize COPT2 inhibitors as valuable tools to investigate the role of copper in biological systems, study the consequences of copper deficiency, and gain insights into the regulatory mechanisms governing copper transport and homeostasis. Consequently, COPT2 inhibitors contribute significantly to advancing our understanding of the intricate interplay between copper and cellular physiology, providing a foundation for future applications in addressing copper-related disorders or conditions beyond the scope of this description.
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ciprofloxacin | 85721-33-1 | sc-217900 | 1 g | $43.00 | 8 | |
Ciprofloxacin inhibits COPT2 by binding to its active site, preventing the enzyme from catalyzing the conversion of its substrate. This disrupts the copper transport system in bacteria, leading to cell death. | ||||||
Levofloxacin | 100986-85-4 | sc-252953 sc-252953B sc-252953A | 10 mg 250 mg 1 g | $40.00 $46.00 $54.00 | 3 | |
Levofloxacin, like Ciprofloxacin, inhibits COPT2 by binding to the enzyme's active site, hindering copper uptake in bacterial cells, and ultimately causing bacterial death. | ||||||
Penicillamine | 52-67-5 | sc-205795 sc-205795A | 1 g 5 g | $46.00 $96.00 | ||
Penicillamine chelates copper ions, reducing their availability for cellular uptake by COPT2. It is used in Wilson's disease to lower copper levels in the body. | ||||||
Ammonium tetrathiomolybdate | 15060-55-6 | sc-239242 sc-239242A sc-239242B sc-239242C | 1 g 10 g 25 g 50 g | $47.00 $203.00 $421.00 $525.00 | ||
Ammonium tetrathiomolybdate forms a complex with copper in the gastrointestinal tract, reducing copper absorption and availability to COPT2 transporters. | ||||||
Neocuproine | 484-11-7 | sc-257893 sc-257893A sc-257893B sc-257893C sc-257893D | 1 g 5 g 25 g 100 g 250 g | $34.00 $90.00 $297.00 $1108.00 $2388.00 | 1 | |
Neocuproine is another copper chelator that can disrupt copper homeostasis by binding to copper ions and blocking their uptake by COPT2. | ||||||
Carbamazepine | 298-46-4 | sc-202518 sc-202518A | 1 g 5 g | $33.00 $71.00 | 5 | |
Carbamazepine indirectly inhibits COPT2 by reducing the expression of this transporter in cells, leading to decreased copper uptake. | ||||||
Zinc | 7440-66-6 | sc-213177 | 100 g | $48.00 | ||
1-Hydroxypyridine-2-thione zinc salt can inhibit COPT2 by releasing zinc ions, which can compete with copper for binding to the transporter and inhibit copper uptake. | ||||||
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $53.00 $89.00 | 7 | |
Disulfiram can indirectly inhibit COPT2 by blocking the enzyme superoxide dismutase, leading to the accumulation of toxic copper ions in cells. | ||||||