CUTC inhibitors are a class of chemical compounds that specifically target the CUTC (Copper Transporter C) protein, which is involved in the intracellular transport and homeostasis of copper ions. CUTC plays a critical role in maintaining the proper distribution of copper within the cell, a trace element that is essential for the function of various enzymes and proteins, including those involved in energy production and antioxidant defense. The protein is responsible for ensuring copper is delivered to the right cellular compartments while preventing toxic accumulation. Inhibitors of CUTC work by disrupting its copper transport function, either by interfering with its ability to bind copper ions or by blocking its interaction with other cellular components involved in copper trafficking.
Chemically, CUTC inhibitors are often small molecules designed to target specific sites within the protein where copper binding or transport occurs. These inhibitors may function by binding to the copper-binding domains of CUTC, preventing the protein from facilitating the transfer of copper ions to their proper cellular destinations. Alternatively, they may disrupt the conformational changes necessary for CUTC to transport copper effectively, impacting the overall balance of copper within the cell. By studying CUTC inhibitors, researchers gain insights into the molecular mechanisms governing copper transport and homeostasis. This helps in understanding how alterations in copper metabolism can affect broader biological processes, such as enzyme function and oxidative stress regulation, and how copper is distributed across different organelles and compartments within the cell.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $53.00 $89.00 | 7 | |
Disulfiram chelates copper ions, which may decrease the availability of copper for CUTC, thereby inhibiting its normal enzymatic function. | ||||||
Bathocuproine | 4733-39-5 | sc-257115 | 500 mg | $52.00 | ||
Bathocuproine selectively binds to copper(I), possibly preventing copper from interacting with CUTC, which is essential for its activity. | ||||||
Penicillamine | 52-67-5 | sc-205795 sc-205795A | 1 g 5 g | $46.00 $96.00 | ||
Penicillamine has a high affinity for copper ions, which may lead to a reduction in copper bioavailability required for the catalytic function of CUTC. | ||||||
Zinc | 7440-66-6 | sc-213177 | 100 g | $48.00 | ||
Zinc acetate may compete with copper for binding sites, potentially reducing copper ion availability for CUTC and its activity. | ||||||
L-Mimosine | 500-44-7 | sc-201536A sc-201536B sc-201536 sc-201536C | 25 mg 100 mg 500 mg 1 g | $36.00 $88.00 $220.00 $436.00 | 8 | |
Mimosine has the ability to chelate metal ions, which could interfere with the metalloenzyme activity of CUTC by sequestering its copper cofactor. | ||||||
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 a copper(I) chelator, which may prevent copper from being properly integrated into CUTC, thus indirectly inhibiting its function. | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $110.00 $250.00 $936.00 $50.00 | 33 | |
Quercetin has been observed to chelate metal ions, which could decrease the copper ion availability necessary for the enzymatic activity of CUTC. | ||||||
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 complexes with copper, which might reduce the copper ion concentration required for the catalytic activity of CUTC. | ||||||