Date published: 2025-11-3

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C14orf54 Activators

C14orf54 Activators encompass a diverse group of chemical compounds that, while not directly interacting with C14orf54, facilitate its functional activity within its associated signaling pathways. Forskolin, by increasing cAMP, and IBMX, through inhibiting phosphodiesterases, both raise the levels of cyclic nucleotides, leading to the activation of PKA and other cAMP/cGMP-dependent kinases; this can indirectly result in the phosphorylation of C14orf54 or its partners, enhancing its signaling capacity. Similarly, PMA stimulates PKC, potentially phosphorylating C14orf54-related proteins and amplifying its activity in PKC-dependent pathways. Ionomycin and A23187, both acting as calcium ionophores, elevate intracellular calcium levels, which may activate calcium-dependent kinases that target C14orf54 for activation. Calyculin A and Okadaic acid, as phosphatase inhibitors, prevent the dephosphorylation of proteins within the C14orf54 pathway, possibly maintaining C14orf54 in an active state.

Further supporting the activity of C14orf54, Anisomycin, through the induction of stress-activated protein kinases, could lead to the activation of C14orf54 in response to cellular stress or apoptotic signals. The cAMPand cGMP analogs, 8-Br-cAMP and 8-Br-cGMP, mimic the effects of the endogenous cyclic nucleotides, potentially activating PKA or PKG, respectively, and thus promoting the activation of C14orf54 through these kinase pathways. Thapsigargin, by inhibiting the SERCA pump, causes an increase in cytosolic calcium, which can subsequently activate calcium-dependent signaling cascades that involve C14orf54. Finally, Staurosporine, despite being a broad-spectrum kinase inhibitor, may paradoxically enhance the functional activity of C14orf54 by inhibiting kinases that normally suppress C14orf54's signaling pathways, thereby allowing for an increase in the protein's functional activity. Collectively, these activators work through distinct but interconnected biochemical mechanisms to enhance the activity of C14orf54, ensuring the protein's participation in the proper functioning of its associated cellular signaling networks.

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