The compounds listed above can indirectly modulate the activity of Syne-1 by influencing related cellular structures and signaling pathways. All-trans Retinoic Acid and Staurosporine, for example, can affect gene expression and kinase signaling, respectively, both of which are essential to the functional regulation of Syne-1. Y-27632 and Blebbistatin specifically target components of the cytoskeleton, which is closely linked to Syne-1's role in nuclear positioning and cellular mechanics. Nocodazole and Cytochalasin D disrupt microtubules and actin filaments, respectively, thereby potentially impacting Syne-1's interactions with these cytoskeletal elements. Paclitaxel stabilizes microtubules, providing a contrasting effect that may also influence Syne-1 functions.
Vorinostat and Rapamycin are examples of compounds that modulate chromatin structure and cellular signaling pathways, respectively. These alterations in cellular dynamics can indirectly influence the activity of Syne-1 within the LINC complex. LY294002, as a PI3K inhibitor, impacts signaling pathways that could be relevant to the regulation of Syne-1. Lastly, A23187 and Verapamil, by modulating calcium signaling, can affect a range of cellular processes, including those in which Syne-1 is involved.
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