Date published: 2025-9-5

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cytohesin-1 Inhibitors

Cytohesin-1 inhibitors encompasses a range of chemical compounds specifically designed to interact with and modulate the activity of Cytohesin-1, a key player in intracellular signaling. This group includes direct inhibitors, such as SecinH3, which are structured to specifically target the interaction of Cytohesin-1 with ARF proteins. These inhibitors function by binding to essential interaction domains within Cytohesin-1, effectively blocking its association with ARF proteins. This inhibition leads to significant alterations in cellular processes, particularly those involving the GTPase activity of ARF proteins. These proteins play a pivotal role in various cellular mechanisms, including vesicular trafficking and the regulation of the cytoskeleton. The chemical structures of these direct inhibitors are often intricate, designed to fit precisely within the specific protein-protein interaction sites, thereby ensuring efficacy and specificity in their mode of action. indirect inhibitors of Cytohesin-1 target broader aspects of cellular signaling pathways that are either influenced by or intersect with Cytohesin-1 functions. These include inhibitors of pathways such as the PI3K/AKT pathway and the MAP kinase pathways, as well as inhibitors targeting Src family kinases. Chemical compounds like LY294002 and Wortmannin, which inhibit PI3K, and kinase inhibitors like Dasatinib and PP2, exemplify this approach. Their chemical structures vary widely, reflecting the diversity of targets within these complex signaling pathways. By modulating these pathways, indirect inhibitors can affect Cytohesin-1's functionality in a roundabout way, altering its role in various cellular processes. This broad spectrum of chemical entities, ranging from small molecular inhibitors to larger organic molecules, demonstrates the complexity and intricacy of cellular signaling networks and highlights the multifaceted nature of Cytohesin-1 within these networks. Through the use of both direct and indirect inhibitors, researchers can gain valuable insights into the diverse biological functions and mechanisms of action of Cytohesin-1.

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