Date published: 2025-9-15

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RGL2 Inhibitors

RGL2 inhibitors encompass a category of chemicals that modulate cellular signaling pathways in which RGL2 is a participant or has an influence. These inhibitors do not directly target RGL2 but rather the broader signaling cascades that RGL2 might affect, such as MAPK/ERK, PI3K/AKT, and Rho GTPase pathways. The inhibition strategies include the use of small molecules that interfere with kinases and other proteins that are either upstream or downstream of RGL2 in these pathways.

The inhibitors function by altering the activity of kinases like CDK4/6, MEK, and AKT or by disrupting the interactions of small GTPases, which are pivotal elements in signaling pathways regulated by RGL2. For instance, PD 0332991 and CCT128930 are kinase inhibitors that can arrest the cell cycle and prevent survival signals, respectively, thereby counteracting the cell proliferation and survival effects RGL2 may promote through these pathways. Other chemicals, such as LY294002 and Wortmannin, are PI3K inhibitors that can reduce AKT activation, thereby impeding any RGL2-mediated signaling through the PI3K/AKT pathway, which is often linked to cell growth and survival. Similarly, U0126 and PD 98059 are specific MEK inhibitors that prevent the activation of the ERK pathway, which could be critical in RGL2-related signaling mechanisms.

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