Date published: 2025-11-24

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DENND5B Inhibitors

Chemical inhibitors of DENND5B can exert their inhibitory effects through different mechanisms, primarily by interfering with the protein's role in vesicular trafficking and membrane dynamics. Go6976 is one such inhibitor that targets Protein Kinase C (PKC), a kinase that is instrumental in the regulation of DENND5B. By inhibiting PKC, Go6976 can disrupt the phosphorylation-dependent processes that are required for DENND5B to perform its function in vesicular trafficking. Similarly, Dynasore and Dyngo-4a, both dynamin inhibitors, can impair DENND5B-mediated endocytic processes by preventing the scission of vesicles from the plasma membrane. This action effectively blocks the essential step in endocytic trafficking that DENND5B is associated with.

Furthermore, DENND5B's function is closely linked with the actin cytoskeleton and related signaling pathways. Chemicals like Latrunculin B disrupt actin polymerization, thus potentially impairing the DENND5B-mediated cytoskeletal changes that are critical for vesicle transport. In a related manner, SMIFH2, by inhibiting formin, can alter actin filament assembly and dynamics, leading to the functional inhibition of DENND5B. Moreover, inhibitors like ML141 and ZCL278, which target the GTPases Cdc42 and Rho, respectively, can reduce the vesicular trafficking function of DENND5B by altering GTPase-dependent signaling pathways. NSC23766, which inhibits Rac1, and Y-27632, which inhibits ROCK, can also affect DENND5B's role in cell migration and vesicular trafficking by disrupting signals that govern the actin cytoskeleton. Lastly, Blebbistatin, by inhibiting myosin II, can affect cell contractility and motility, thereby impacting the cellular functions that DENND5B is involved in. Each of these chemicals disrupts specific signaling pathways or cellular processes that are essential for DENND5B's function, leading to its functional inhibition.

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