Date published: 2025-9-14

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HMSD Activators

Chemical activators of HMSD can initiate a cascade of intracellular events leading to its functional activation. Forskolin is one such activator, known to directly stimulate adenylate cyclase, subsequently increasing intracellular cAMP levels. The rise in cAMP activates protein kinase A (PKA), which can then target HMSD for phosphorylation, resulting in its functional activation. Similarly, IBMX contributes to the elevation of cAMP levels by inhibiting phosphodiesterases, thereby preventing the degradation of cAMP and facilitating a supportive environment for PKA to activate HMSD through phosphorylation. Moreover, direct PKC activators like PMA and Phorbol 12-myristate 13-acetate (PMA) have the capacity to activate PKC, which in turn can phosphorylate and activate HMSD. The increase in intracellular calcium levels by agents such as Ionomycin also contributes to the activation of calcium-dependent kinases, which have the potential to phosphorylate and activate HMSD.

The disruption of calcium homeostasis by Thapsigargin can indirectly lead to the activation of calcium-dependent kinases capable of HMSD phosphorylation. The inhibition of protein phosphatases by compounds like Calyculin A and Okadaic Acid results in an increase in the phosphorylated state of cellular proteins, including HMSD, leading to its functional activation. Dibutyryl-cAMP, a cell-permeable cAMP analog, similarly activates PKA, contributing to the phosphorylation and activation of HMSD. Additionally, Anisomycin's activation of MAPK pathways can lead to the functional activation of HMSD through downstream kinase activity. Chelerythrine's complex role in cellular signaling, while primarily known as a PKC inhibitor, can also instigate compensatory cellular responses that lead to the activation of kinases which phosphorylate HMSD. Lastly, the activation of AMP-activated protein kinase (AMPK) by Epigallocatechin Gallate can also result in the activation of HMSD through its downstream signaling effects. Each of these chemicals targets specific cellular pathways that are known to influence the phosphorylation state and subsequent activation of HMSD, thereby modulating its activity without affecting protein expression levels.

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