Date published: 2025-11-2

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Prickle2 Inhibitors

Prickle2 inhibitors are a class of chemical compounds that specifically target and inhibit the function of the Prickle2 protein, which is part of the broader Prickle family of proteins. These proteins are involved in a variety of cellular processes, including planar cell polarity (PCP) signaling, which is essential for the proper organization and orientation of cells within tissues. Prickle2 is associated with intracellular signaling pathways that regulate cytoskeletal organization and cellular polarity. Inhibition of Prickle2 activity can alter these signaling pathways, leading to changes in cellular behavior, such as modifications in cell migration, adhesion, and morphology. The molecular mechanism of Prickle2 involves its interactions with other proteins, such as Disheveled (Dvl) and Van Gogh-like proteins (Vangl), which are critical in the PCP pathway. By interfering with these interactions, Prickle2 inhibitors can modulate the downstream effects of PCP signaling.

Chemically, Prickle2 inhibitors can vary in structure, but they often contain moieties that allow them to interact specifically with the protein domains responsible for its signaling functions. These inhibitors may function by preventing the protein-protein interactions necessary for Prickle2 to mediate its effects on cellular polarity, or by interfering with its localization within the cell. Such structural inhibition can lead to significant downstream changes in cellular pathways, altering the organization of the cytoskeleton and impacting cellular processes like axon guidance and synaptic development. The precise design of these inhibitors is often based on the structural analysis of Prickle2 and its interaction partners, allowing for selective inhibition without affecting other related proteins. This chemical specificity is important for ensuring that the inhibitors target Prickle2-mediated pathways without off-target effects on other cellular functions.

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