Date published: 2026-6-15

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GAP-assoc p190 Inhibitors

P190RhoGAP inhibitors are a class of chemical compounds specifically designed to modulate the activity of the GAP-associated p190 protein, which plays a significant role in the regulation of Rho GTPases. These GTPases are pivotal in controlling various cellular processes, including cytoskeletal reorganization, cell proliferation, and migration. The inhibitors function by directly or indirectly altering the activity of GAP-associated p190, thereby affecting the GTPase signaling pathways. By doing so, they can regulate the activity levels of RhoA, which is a key molecule in the formation of stress fibers and focal adhesions, a process vital for maintaining cellular shape and motility. The mechanisms by which these inhibitors exert their effect can vary but are centered on the principle of disrupting the normal function of GAP-associated p190. Some compounds achieve this by binding directly to p190, altering its conformation and thus its function. Others act on proteins or processes upstream or downstream of p190, thereby altering its activity indirectly. For instance, inhibitors that affect the prenylation of Rho GTPases can alter the localization and function of RhoA, which in turn can modulate the activity of GAP-associated p190. Similarly, compounds that inhibit RhoA-mediated transcription can influence GAP-associated p190 by altering its signaling pathways. These methods are grounded in the intricate network of cellular signaling, where the regulation of one molecule can have cascading effects on others within the same pathway. The precise mechanism of each inhibitor varies depending on its structure and target within the Rho GTPase signaling cascade, but the overarching goal remains the modulation of GAP-associated p190 activity to achieve the desired cellular outcome.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

N-[5-[(4-Ethyl-1-piperazinyl)methyl]-2-pyridinyl]-5-fluoro-4-[4-fluoro-2-methyl-1-(1-methylethyl)-1H-benzimidazol-6-yl]-2-pyrimidinamine Methanesulfonate

1231930-82-7sc-496536
2.5 mg
$398.00
(0)

A selective CDK4/6 inhibitor.

PHA-848125

802539-81-7sc-364581
sc-364581A
5 mg
10 mg
$304.00
$555.00
(0)

Targets multiple CDKs including CDK4/6 and has shown potential in hepatocellular carcinoma.

Flavopiridol

146426-40-6sc-202157
sc-202157A
5 mg
25 mg
$78.00
$259.00
41
(3)

A broad-spectrum CDK inhibitor, impacting several CDKs including CDK4/6.

Dinaciclib

779353-01-4sc-364483
sc-364483A
5 mg
25 mg
$247.00
$888.00
1
(0)

Another broad-spectrum CDK inhibitor, known for its potency against CDK4/6.

Roscovitine

186692-46-6sc-24002
sc-24002A
1 mg
5 mg
$94.00
$265.00
42
(2)

Primarily inhibits CDK2, but also affects CDK4/6, used in various cancer research contexts.

BMS-265246

582315-72-8sc-364440
sc-364440A
5 mg
10 mg
$304.00
$555.00
(0)

BMS-265246 is a potent and selective inhibitor that targets the kinase activity of Bmx through competitive binding to the ATP-binding site. This interaction obstructs the phosphorylation process essential for Bmx activation and subsequent signal transduction pathways.