Date published: 2025-9-15

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HSBP1 Activators

Chemical activators of HSBP1 include a range of compounds that influence intracellular signaling pathways leading to the protein's activation. Forskolin, by directly stimulating adenylyl cyclase, elevates cAMP levels, which in turn activate protein kinase A (PKA). The activated PKA can phosphorylate HSBP1, thus enabling its activation. Similarly, Dibutyryl cAMP and 8-Br-cAMP, both analogs of cAMP, permeate cellular membranes and directly activate PKA, which can then phosphorylate HSBP1. Phorbol 12-myristate 13-acetate (PMA) specifically activates protein kinase C (PKC), which is known to phosphorylate a broad range of cellular proteins, including HSBP1. Anisomycin triggers stress-activated protein kinases, which have the capacity to phosphorylate HSBP1, leading to its activation. These kinases, once activated, can target HSBP1, adding a phosphate group to activate the protein.

Other chemicals act by modulating cellular phosphatase and kinase activity levels. Calyculin A and Okadaic Acid, both potent inhibitors of protein phosphatases, lead to an increase in the phosphorylation of proteins. This increase can extend to HSBP1, which when phosphorylated becomes activated. Thapsigargin and Ionomycin both disrupt calcium homeostasis, with Thapsigargin inhibiting the SERCA pump and Ionomycin acting as a calcium ionophore. The resultant rise in intracellular calcium can activate a cascade of calmodulin-dependent kinases, which in turn can phosphorylate HSBP1. Staurosporine, although generally known as a kinase inhibitor, can at lower concentrations activate certain kinases that may phosphorylate and thus activate HSBP1. Lastly, Epigallocatechin gallate (EGCG) and Zinc Pyrithione can influence kinase and phosphatase activities, which can alter the phosphorylation state of HSBP1, leading to its functional activation through changes in the balance of cellular signaling.

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