Date published: 2025-10-29

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DCDC2C Activators

Chemical activators of DCDC2C include a variety of compounds that interact with the protein in different ways to induce its functional activity. Zinc acetate provides zinc ions, which can bind to DCDC2C, possibly resulting in a conformational change that stabilizes the protein's functional form. Similarly, magnesium sulfate supplies magnesium ions that can act as essential cofactors, enhancing the enzymatic activity of DCDC2C. Calcium chloride, by contributing calcium ions, can also prompt structural modifications in DCDC2C that lead to its activation, as calcium-binding often influences protein function. Additionally, sodium orthovanadate functions by inhibiting phosphatases that would otherwise dephosphorylate and inactivate DCDC2C, thereby maintaining DCDC2C in an active state through sustained phosphorylation.

Further activation of DCDC2C can be facilitated by forskolin, which boosts intracellular cyclic AMP (cAMP) levels, leading to the activation of protein kinase A (PKA). PKA can phosphorylate DCDC2C, thereby activating it. Phorbol 12-myristate 13-acetate (PMA) activates protein kinase C (PKC), which can similarly phosphorylate and activate DCDC2C. Ionomycin raises intracellular calcium levels, which may activate calcium-dependent kinases that are capable of phosphorylating DCDC2C. Hydrogen peroxide is known for its ability to induce oxidative modifications in proteins, and in the case of DCDC2C, this can translate to activation through oxidatively induced structural changes. S-Nitroso-N-acetylpenicillamine (SNAP) can lead to the S-nitrosylation of DCDC2C, a covalent modification that can activate the protein. The signaling molecule 8-Bromo-cyclic AMP serves as a cAMP analog that activates PKA, which, in turn, can phosphorylate DCDC2C. Thapsigargin disrupts calcium stores and can indirectly activate DCDC2C through the activation of calcium-dependent kinases. Lastly, epidermal growth factor triggers a cascade of phosphorylation events in the cell, one of which may directly result in the phosphorylation and subsequent activation of DCDC2C. Each of these chemicals engages with DCDC2C or its regulatory pathways, leading to an increase in its functional activity within the cellular environment.

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