Gas6 inhibitors belong to a distinctive class of chemical compounds that primarily target the Gas6 protein and its associated signaling pathways. Gas6, short for Growth Arrest-Specific 6, is a vitamin K-dependent protein that plays a crucial role in mediating cellular processes such as cell survival, proliferation, migration, and adhesion. The inhibitors designed to interact with Gas6 typically act by disrupting its binding to its receptor family known as TAM (Tyro3, Axl, and Mer). This receptor family is implicated in regulating immune responses, clearance of apoptotic cells, tissue homeostasis, and platelet aggregation. Gas6 inhibitors function by competitively binding to Gas6 or its receptor sites, consequently impeding the natural Gas6-receptor interactions and downstream signaling cascades.
The structural diversity of Gas6 inhibitors allows for a range of approaches in designing compounds that can effectively disrupt the Gas6 signaling pathway. These inhibitors often target specific binding sites on Gas6 or the TAM receptors, obstructing the ligand-receptor interaction necessary for downstream intracellular responses. The underlying rationale behind Gas6 inhibition lies in the modulation of cellular processes that rely on the Gas6-TAM signaling axis. By attenuating these interactions, Gas6 inhibitors have the capacity to impact various cellular functions that are otherwise influenced by the Gas6-mediated signaling. Due to the critical role of Gas6 in cellular growth, differentiation, and immune modulation, inhibitors targeting this system hold promise for a variety of applications.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Bemcentinib | 1037624-75-1 | sc-507363 | 10 mg | $900.00 | ||
R428 is a small molecule inhibitor that targets the Axl receptor kinase, disrupting the Axl/Gas6 interaction and downstream signaling pathways involved in cell proliferation, survival, and migration. It has shown potential as an anti-cancer agent in research studies. | ||||||
BMS 777607 | 1025720-94-8 | sc-364438 sc-364438A | 10 mg 50 mg | $400.00 $1269.00 | 1 | |
BMS-777607 is a potent inhibitor of Axl, Mer, and Tyro3 receptor kinases, disrupting the Gas6-mediated activation of these receptors. By interfering with this interaction, the inhibitor hampers tumor growth, angiogenesis, and metastasis, offering therapeutic potential in cancer research. | ||||||
(1r,4r)-4-((2-(Butylamino)-5-(5-(morpholinomethyl)pyridin-2-yl)pyrimidin-4-yl)amino)cyclohexanol | 1493694-70-4 | sc-504477 | 5 mg | $255.00 | ||
UNC2250 is a potent and selective Axl inhibitor that disrupts the Gas6/Axl interaction. By binding to the ATP-binding site of Axl, it impedes kinase activity and downstream signaling pathways. This mechanism positions UNC2250 as a potential anti-cancer agent, particularly in situations involving Axl overexpression. | ||||||