STK31 inhibitors constitute a specific class of small molecules designed to selectively target and modulate the activity of the STK31 kinase enzyme. STK31, also known as serine/threonine kinase 31 or TAO kinase 2 (TAOK2), is a member of the Ste20-like kinase family. These inhibitors are engineered with the primary objective of influencing the cellular processes regulated by STK31.
At the molecular level, STK31 inhibitors exert their effects by binding to the ATP-binding site within the catalytic domain of the kinase. This binding event disrupts the kinase's ability to phosphorylate downstream substrates by inhibiting ATP from accessing the active site. Essentially, STK31 is a serine/threonine kinase that plays a pivotal role in several intracellular signaling cascades, particularly those involved in cell cycle regulation and cytoskeletal dynamics. Inhibition of STK31 by these small molecules impacts the balance of phosphorylation events in the cell, thereby modulating cellular functions related to cell division, migration, and proliferation.Moreover, STK31 inhibitors are known for their specificity, often exhibiting selectivity towards STK31 over other kinases within the broader kinome. This selectivity is crucial for minimizing off-target effects and ensuring that the inhibitor's action remains focused on STK31-mediated processes. By elucidating the precise mechanism through which STK31 inhibitors interfere with kinase activity, researchers aim to gain valuable insights into the underlying molecular pathways that govern cell behavior, which could have broader implications in understanding basic cellular biology andunlocking new avenues for future research in various fields.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Hesperadin | 422513-13-1 | sc-490384 | 10 mg | $304.00 | ||
Hesperadin is a selective inhibitor of STK31, which acts by binding to the ATP-binding site of the kinase, blocking its activity. | ||||||
AZD7762 | 860352-01-8 | sc-364423 | 2 mg | $107.00 | ||
AZD-7762 inhibits STK31 through competitive binding to the ATP-binding site, interrupting kinase activity. | ||||||
RO-3306 | 872573-93-8 | sc-358700 sc-358700A sc-358700B | 1 mg 5 mg 25 mg | $66.00 $163.00 $326.00 | 37 | |
Ro-3306 is a potent STK31 inhibitor that inhibits kinase activity by blocking the ATP-binding site. | ||||||
BI 2536 | 755038-02-9 | sc-364431 sc-364431A | 5 mg 50 mg | $151.00 $525.00 | 8 | |
BI-2536 is a selective STK31 inhibitor that interferes with kinase activity by binding to its ATP pocket. | ||||||
Tozasertib | 639089-54-6 | sc-358750 sc-358750A | 25 mg 50 mg | $62.00 $87.00 | 4 | |
VX-680, also known as Tozasertib, inhibits STK31 by targeting its ATP-binding site, blocking kinase activity. | ||||||
R547 | 741713-40-6 | sc-364596 sc-364596A | 2 mg 5 mg | $375.00 $395.00 | ||
R547 inhibits STK31 by binding to the ATP-binding pocket of the kinase, inhibiting its activation. | ||||||
GSK461364 | 929095-18-1 | sc-364504 sc-364504A | 10 mg 50 mg | $500.00 $1540.00 | ||
GSK461364A inhibits STK31 by competitively binding to its ATP-binding site, inhibiting kinase activation. | ||||||