Date published: 2025-10-21

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Rac Inhibitors

Santa Cruz Biotechnology now offers a broad range of Rac inhibitors for use in various applications. Rac inhibitors are a specialized class of chemicals that target and inhibit the activity of Rac proteins, which are part of the Rho family of GTPases. These proteins play a critical role in regulating the cytoskeleton, cell movement, and various signaling pathways. In scientific research, Rac inhibitors are invaluable for studying cellular processes such as cell migration, adhesion, and morphology. They are also crucial in investigating the molecular mechanisms underlying diseases such as cancer, where abnormal Rac activity can lead to unchecked cell proliferation and metastasis. By selectively inhibiting Rac proteins, researchers can dissect the contributions of these proteins to specific cellular functions and signaling pathways. The availability of a diverse selection of Rac inhibitors allows scientists to choose compounds with different specificities and potencies, enabling more precise and nuanced studies. This range supports a wide array of experimental designs, from basic biochemical assays to complex in vivo studies. View detailed information on our available Rac inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Toxin A from Clostridium difficile

sc-222361
sc-222361A
2 µg
100 µg
$192.00
$772.00
(1)

Toxin A from Clostridium difficile is a potent glucosyltransferase that modifies Rho GTPases, disrupting cellular signaling pathways. Its enzymatic activity leads to actin cytoskeleton disassembly, promoting cell rounding and apoptosis. The toxin's specificity for certain Rho family proteins highlights its unique interaction dynamics. Additionally, Toxin A's ability to induce inflammatory responses showcases its role in altering host immune mechanisms, further complicating cellular responses.

EHT 1864

754240-09-0sc-361175
sc-361175A
10 mg
50 mg
$209.00
$872.00
12
(2)

EHT 1864 acts as a potent Rac inhibitor, selectively modulating the activity of Rho family GTPases. Its unique binding affinity allows it to disrupt the nucleotide exchange process, effectively altering downstream signaling cascades. The compound exhibits distinct kinetic properties, facilitating rapid inhibition of Rac-mediated pathways. This selective interaction leads to significant changes in cellular dynamics, influencing processes such as migration and adhesion through targeted molecular interference.

Ras/Rac Transformation Blocker, SCH 51344

171927-40-5sc-204231
10 mg
$146.00
4
(1)

SCH 51344 serves as a specialized Ras/Rac transformation blocker, exhibiting a unique mechanism of action through its interaction with GTPase proteins. By stabilizing the inactive form of Rac, it effectively impedes the nucleotide exchange process, leading to altered cellular signaling. Its distinct kinetic profile allows for swift modulation of Rac activity, impacting various cellular functions, including cytoskeletal organization and cellular morphology, through precise molecular engagement.