Date published: 2025-9-15

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ECAT1 Activators

Chemical activators of ECAT1 can influence its activity through various mechanisms that involve the modulation of intracellular signaling pathways. Forskolin is known to be a potent activator of adenylyl cyclase, which in turn increases the levels of cAMP within the cell. The elevated cAMP levels activate protein kinase A (PKA), which can then phosphorylate ECAT1, leading to its activation. Similarly, IBMX acts to sustain increased levels of cAMP by inhibiting phosphodiesterases, thereby preventing the degradation of cAMP. This results in the prolonged activation of PKA, which continues to phosphorylate and activate ECAT1. Phorbol 12-myristate 13-acetate (PMA) engages with protein kinase C (PKC), which has a broad range of target proteins. Activated PKC is capable of phosphorylating ECAT1, thus contributing to its activation.

In addition to these, calcium ionophore A23187 directly elevates intracellular calcium levels, which activates calcium-dependent kinases that can also phosphorylate ECAT1, resulting in its activation. Zinc acetate and magnesium sulfate provide essential metal ion cofactors that can induce conformational changes in ECAT1, essential for its activation. Sodium orthovanadate acts by inhibiting tyrosine phosphatases, leading to a sustained phosphorylated state of proteins, including ECAT1, thereby keeping it active. Okadaic Acid, a specific inhibitor of protein phosphatases 1 and 2A, contributes to the activation of ECAT1 by impeding its dephosphorylation, which is a process that would otherwise render ECAT1 inactive. Anisomycin activates stress-activated protein kinases (SAPKs)/Jun N-terminal kinases (JNK), which can directly phosphorylate and activate ECAT1. Thapsigargin disrupts endoplasmic reticulum calcium stores and can activate ECAT1 through the subsequent activation of calcium-dependent kinases. Hydrogen peroxide introduces oxidative stress, which can initiate signaling cascades that lead to the phosphorylation of ECAT1. Lastly, epidermal growth factor (EGF) engages its receptor to trigger a downstream signaling cascade, culminating in the activation of multiple kinases with the capability to phosphorylate and activate ECAT1, illustrating a diverse range of chemical interactions that can result in the functional activation of ECAT1.

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