Date published: 2026-7-9

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STEAP Inhibitors

STEAP inhibitors are a class of chemical compounds specifically designed to target and inhibit the function of Six Transmembrane Epithelial Antigen of the Prostate (STEAP) proteins, a family of metalloreductases involved in the reduction of metal ions such as iron (Fe³⁺ to Fe²⁺) and copper (Cu²⁺ to Cu¹⁺) within cells. The STEAP family includes several members, such as STEAP1, STEAP2, STEAP3, and STEAP4, each playing distinct roles in cellular metal homeostasis, redox balance, and metabolic processes. These proteins are primarily localized in the membranes of endosomes, lysosomes, and the plasma membrane, where they facilitate the uptake and utilization of essential metal ions, which are crucial for various cellular functions, including enzyme activity, electron transport, and DNA synthesis. By inhibiting STEAP proteins, researchers can interfere with these metal ion reduction processes, providing a valuable tool to study the specific roles of STEAP proteins in metal metabolism and their broader implications for cellular function.

In research, STEAP inhibitors are valuable for exploring the molecular mechanisms by which STEAP proteins contribute to cellular metal homeostasis and the broader effects of disrupting these processes. By blocking the activity of STEAP proteins, scientists can investigate how the inhibition affects the intracellular availability of reduced metal ions, particularly iron and copper, and the subsequent impact on processes that depend on these metals, such as mitochondrial respiration, DNA repair, and oxidative stress responses. This inhibition allows researchers to study the role of STEAP proteins in maintaining redox balance and how imbalances in metal ion levels can lead to cellular dysfunction. Additionally, STEAP inhibitors enable the examination of the interactions between STEAP proteins and other components of the metal transport and redox systems, providing insights into the complex regulatory networks that govern metal ion homeostasis and their importance in various biological contexts. Through these studies, the use of STEAP inhibitors enhances our understanding of the critical role of metalloreductases in cellular physiology, the regulation of metal ion metabolism, and the broader implications of these processes for cell survival and function.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Deferoxamine mesylate

138-14-7sc-203331
sc-203331A
sc-203331B
sc-203331C
sc-203331D
1 g
5 g
10 g
50 g
100 g
$255.00
$1060.00
$2923.00
$4392.00
$8333.00
19
(1)

Deferoxamine is an iron chelator that can indirectly affect STEAP proteins by modulating cellular iron levels, which are crucial for STEAP function.

Sodium metavanadate

13718-26-8sc-251034
sc-251034A
5 g
25 g
$32.00
$84.00
3
(1)

Tetrathiomolybdate is a copper chelating agent, potentially impacting STEAP functions by modulating intracellular copper levels.

Curcumin

458-37-7sc-200509
sc-200509A
sc-200509B
sc-200509C
sc-200509D
sc-200509F
sc-200509E
1 g
5 g
25 g
100 g
250 g
1 kg
2.5 kg
$37.00
$69.00
$109.00
$218.00
$239.00
$879.00
$1968.00
47
(1)

Curcumin, known for its antioxidant properties, could indirectly affect STEAP proteins by modulating oxidative stress-related pathways.

Disulfiram

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

Disulfiram, a drug used for alcohol dependence, can chelate copper and might indirectly affect STEAP activity by altering copper metabolism.

Penicillamine

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

D-Penicillamine, a copper chelating agent, could indirectly modulate STEAP activity by influencing copper homeostasis in cells.

Ferrous Sulfate (Iron II Sulfate) Heptahydrate

7782-63-0sc-211505
sc-211505A
250 g
500 g
$73.00
$109.00
(1)

Iron supplementation, like Ferrous Sulfate, can indirectly influence STEAP activity by affecting iron homeostasis in the body.

Clioquinol

130-26-7sc-201066
sc-201066A
1 g
5 g
$45.00
$115.00
2
(1)

Clioquinol, a metal chelator with antibiotic properties, could indirectly influence STEAP function by modulating metal ion levels in cells.