Date published: 2025-9-13

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CDRT15L Activators

Chemical activators of CDRT15L include a variety of compounds that engage distinct biochemical pathways to promote the protein's functional state. Adenosine triphosphate (ATP) is a primary energy source that can activate CDRT15L through phosphorylation processes, which are essential for many proteins to become functionally active. Similarly, magnesium chloride provides magnesium ions, crucial cofactors for many cellular processes, including those that may be needed for CDRT15L to achieve its active conformation. Sodium fluoride acts by maintaining CDRT15L in a phosphorylated state through the inhibition of phosphatase enzymes, preventing the deactivation of the protein. Phorbol 12-myristate 13-acetate (PMA) and 1,2-Dioctanoyl-sn-glycerol (DiC8) both serve as activators of protein kinase C (PKC), which is known to phosphorylate target proteins like CDRT15L, leading to their activation.

In parallel, forskolin drives the activation of CDRT15L by increasing cyclic AMP (cAMP) levels, which in turn activates protein kinase A (PKA), a kinase that can phosphorylate and activate the protein. Ionomycin elevates intracellular calcium levels, triggering calcium-dependent kinases that may phosphorylate CDRT15L. Calmodulin, by activating calmodulin-dependent kinases, also contributes to the activation of CDRT15L through phosphorylation. Okadaic acid, on the other hand, preserves the phosphorylated state of CDRT15L by inhibiting phosphatases, ensuring sustained activation of the protein. Epidermal growth factor (EGF) stimulates its receptor and associated downstream signaling pathways, which can include kinases that target CDRT15L for activation. Additionally, hydrogen peroxide serves as a signaling molecule that can activate kinases which, in turn, activate CDRT15L through redox-mediated signaling pathways. Lastly, lithium chloride indirectly supports the activation of CDRT15L by inhibiting glycogen synthase kinase-3 (GSK-3), a negative regulator of several signaling pathways, potentially leading to an environment conducive to CDRT15L activation.

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