Date published: 2025-9-16

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C8β Inhibitors

The class of C8β inhibitors comprises a diverse set of compounds that either directly or indirectly modulate the activity of the C8β protein, which is involved in intracellular calcium signaling. One such inhibitor, RU360, specifically targets the mitochondrial calcium uniporter (MCU), preventing excessive calcium uptake into the mitochondria. This indirect inhibition influences C8β by impacting calcium-dependent signaling pathways, providing a precise means to modulate cellular processes related to C8β function. Nifedipine, a dihydropyridine calcium channel blocker, indirectly affects C8β by inhibiting L-type calcium channels. The blockade of calcium influx with Nifedipine can modulate cellular processes related to calcium-dependent pathways, impacting C8β function. KN-62, a specific CaMKII inhibitor, indirectly modulates C8β by targeting the calcium/calmodulin-dependent protein kinase II (CaMKII) pathway. As C8β is involved in calcium-dependent signaling, the inhibition of CaMKII by KN-62 influences cellular processes related to calcium signaling, impacting C8β function.

FK506 (Tacrolimus) indirectly influences C8β by inhibiting calcineurin. The disruption of calcium-dependent signaling pathways by FK506 affects C8β function, providing an indirect approach to modulate cellular processes associated with C8β. Ruthenium Red, a non-specific inhibitor of mitochondrial calcium uptake, indirectly influences C8β by blocking mitochondrial calcium transport. This inhibition can modulate cellular processes related to calcium-dependent pathways and impact C8β function. Xestospongin C, an inositol trisphosphate receptor (IP3R) antagonist, indirectly modulates C8β by inhibiting IP3R. The inhibition of IP3R can impact cellular processes related to calcium signaling, influencing C8β function. SKF-96365, a non-specific inhibitor of receptor-mediated calcium entry (RMCE), indirectly influences C8β by blocking RMCE. This inhibition can modulate cellular processes related to calcium-dependent pathways and impact C8β function. In summary, the diverse class of C8β inhibitors offers both direct and indirect means to modulate the protein's activity, impacting intracellular calcium signaling and associated cellular processes. The specific mechanisms of action of these inhibitors provide valuable tools for investigating the intricate regulatory networks governing calcium-dependent pathways and their potential connections to C8β.

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