Date published: 2025-11-8

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Eps8 Activators

Eps8 Activators encompass a collection of chemical compounds that enhance the functional activity of Eps8 through various signaling pathways and interactions with the actin cytoskeleton. Phalloidin and Jasplakinolide amplify Eps8's capping and bundling functions by stabilizing actin filaments, ensuring a robust architecture for cellular processes dependent on cytoskeletal dynamics. Blebbistatin and Cytochalasin D, by modulating actin-myosin interactions and inhibiting actin polymerization respectively, create conditions that favor the actin capping activity of Eps8, thus facilitating its role in actin filament maintenance and rearrangement. Latrunculin A, through its preferential binding to actin monomers, increases the pool of available G-actin, indirectly promoting the capping efficiency of Eps8, while Calyculin A, by inhibiting protein phosphatases, might lead to a phosphorylation state that favors Eps8's interaction with actin. ML141 and NSC23766, as inhibitors of the small GTPases CDC42 and Rac1, could potentially skew cellular signaling pathways towards those that enhance Eps8-mediated actin remodeling, integral to cellular protrusion formation and motility.

In addition, PDGF-BB, by activating growth factor signaling pathways, and Forskolin, by increasing intracellular cAMP levels, indirectly foster an environment conducive to Eps8's functional activity in actin reorganization. Manumycin A, through its inhibition of Ras farnesyltransferase, may also potentiate Eps8's role in signaling pathways that influence actin cytoskeletal rearrangements. The collective action of these compounds serves to potentiate the cellular functions of Eps8, specifically in the context of actin filament dynamics, without necessitating the upregulation of its expression or direct activation. This precise modulation of Eps8's activity by diverse chemical activators underscores the intricate regulatory mechanisms that govern cellular cytoskeletal dynamics and the potential for targeted intervention in pathways involving Eps8.

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