Date published: 2026-5-4

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CRIK Inhibitors

CRIK inhibitors constitute a class of small molecules specifically designed to modulate the activity of the Cdc42-related kinase (CRIK). These compounds exert their effects through direct inhibition of CRIK's kinase activity, disrupting its enzymatic function. Direct CRIK inhibitors, such as RK-33 and 5-ITu, target the ATP-binding site of CRIK, competitively inhibiting its kinase function. This inhibition leads to the modulation of cellular processes regulated by CRIK, including cell migration, invasion, and cytoskeletal dynamics. The selectivity of CRIK inhibitors, exemplified by MLN2480 and AZ191, allows researchers to focus on the specific functions of CRIK in different cellular contexts. These inhibitors bind specifically to CRIK, interfering with its kinase activity and influencing downstream signaling pathways. The direct inhibition of CRIK by these compounds provides valuable tools for dissecting the intricate roles of CRIK in cellular processes related to cell proliferation, survival, and migration. CRIK inhibitors, such as SP-6-27, offer insights into the regulatory mechanisms of CRIK in cellular pathways. By disrupting the kinase activity of CRIK, these compounds modulate downstream signaling cascades, highlighting the importance of CRIK in various cellular functions. Additionally, compounds like CP-547632 and TAK-285 provide researchers with versatile tools to explore the specific roles of CRIK in cellular processes such as cytoskeletal dynamics. In conclusion, CRIK inhibitors represent a diverse class of compounds that directly target the kinase activity of CRIK, leading to the modulation of cellular processes in a specific and selective manner. These inhibitors offer valuable tools for researchers aiming to unravel the complex functions of CRIK in different cellular contexts, providing insights into the regulatory mechanisms of this kinase in various cellular processes.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

K-252a

99533-80-9sc-200517
sc-200517B
sc-200517A
100 µg
500 µg
1 mg
$129.00
$214.00
$498.00
19
(2)

K252a is a natural product isolated from the microbial source Nocardiopsis sp. It has been identified as a broad-spectrum inhibitor of protein kinases, including CIT.

5-Iodotubercidin

24386-93-4sc-3531
sc-3531A
1 mg
5 mg
$153.00
$464.00
20
(2)

5-ITu is a selective CRIK inhibitor that directly interferes with CRIK activity. By competitively binding to the ATP-binding site of CRIK, 5-ITu disrupts its kinase function. This direct inhibition influences downstream signaling pathways regulated by CRIK, affecting cellular functions such as cytoskeletal dynamics. The selectivity of 5-ITu for CRIK makes it a useful compound for investigating the specific roles of CRIK in cellular processes.

Y-27632, free base

146986-50-7sc-3536
sc-3536A
5 mg
50 mg
$186.00
$707.00
88
(1)

Y-27632 is a well-known inhibitor of the Rho-associated protein kinase (ROCK) pathway. It has been reported to indirectly inhibit CIT phosphorylation, suggesting a potential link between ROCK and CIT signaling.

TAK 285

871026-44-7sc-364627
sc-364627A
5 mg
10 mg
$405.00
$700.00
(0)

TAK-285 is a CRIK inhibitor that directly interferes with its kinase activity. By binding to the ATP-binding site, TAK-285 disrupts the enzymatic function of CRIK, leading to the modulation of cellular processes such as cell proliferation and survival. This direct inhibition provides researchers with a valuable tool for exploring the specific functions of CRIK in various cellular contexts.

DCC

538-75-0sc-239713
sc-239713A
25 g
100 g
$72.00
$208.00
3
(1)

DCC-2618 is a potent CRIK inhibitor that directly targets its kinase activity. By binding to the ATP-binding site, DCC-2618 disrupts the enzymatic function of CRIK, leading to the modulation of cellular processes such as cell proliferation and survival. This direct inhibition makes DCC-2618 a valuable tool for researchers aiming to investigate the specific roles of CRIK in various cellular contexts.