SEPT6 Activators encompass a diverse range of compounds that influence cellular structures and signaling pathways, which in turn affect the dynamics, assembly, or function of SEPT6. This includes agents that affect microtubule and actin dynamics, such as paclitaxel, nocodazole, and cytochalasin D, which can indirectly influence the organization and function of septin proteins by disrupting the cytoskeleton. The interaction between cytoskeletal elements and septins is crucial for maintaining cellular morphology and completing cytokinesis, processes in which SEPT6 is known to play a role.
On the other hand, small molecules such as forskolin and PMA modulate intracellular signaling pathways, like those mediated by cAMP or PKC, which can lead to alterations in the phosphorylation state of proteins that may interact with or regulate septins. Lithium chloride and MG-132 are examples of chemicals that indirectly affect SEPT6 by influencing the phosphorylation and degradation of septin-associated proteins, respectively. Additionally, stress response inducers like sodium arsenite and DMSO can trigger cellular pathways that influence septin organization. Lastly, compounds that modulate gene expression or protein stability, such as resveratrol and epigallocatechin gallate, also belong to this category, as they may affect the cellular levels and functions of septin proteins, including SEPT6.
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