Date published: 2026-7-20

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CUTC Inhibitors

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.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Disulfiram

97-77-8sc-205654
sc-205654A
50 g
100 g
$53.00
$89.00
7
(1)

Disulfiram chelates copper ions, which may decrease the availability of copper for CUTC, thereby inhibiting its normal enzymatic function.

Bathocuproine

4733-39-5sc-257115
500 mg
$52.00
(0)

Bathocuproine selectively binds to copper(I), possibly preventing copper from interacting with CUTC, which is essential for its activity.

Penicillamine

52-67-5sc-205795
sc-205795A
1 g
5 g
$46.00
$96.00
(0)

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

7440-66-6sc-213177
100 g
$48.00
(0)

Zinc acetate may compete with copper for binding sites, potentially reducing copper ion availability for CUTC and its activity.

L-Mimosine

500-44-7sc-201536A
sc-201536B
sc-201536
sc-201536C
25 mg
100 mg
500 mg
1 g
$36.00
$88.00
$220.00
$436.00
8
(2)

Mimosine has the ability to chelate metal ions, which could interfere with the metalloenzyme activity of CUTC by sequestering its copper cofactor.

Neocuproine

484-11-7sc-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
(1)

Neocuproine is a copper(I) chelator, which may prevent copper from being properly integrated into CUTC, thus indirectly inhibiting its function.

Quercetin

117-39-5sc-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
(2)

Quercetin has been observed to chelate metal ions, which could decrease the copper ion availability necessary for the enzymatic activity of CUTC.

Ammonium tetrathiomolybdate

15060-55-6sc-239242
sc-239242A
sc-239242B
sc-239242C
1 g
10 g
25 g
50 g
$47.00
$203.00
$421.00
$525.00
(1)

Ammonium tetrathiomolybdate complexes with copper, which might reduce the copper ion concentration required for the catalytic activity of CUTC.