Date published: 2026-6-10

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TTP-αL Activators

TTP-αL Activators are a class of compounds that enhance the functional activity of TTP-αL through direct or indirect interactions. They work through various signaling pathways that TTP-αL is directly involved in. Forskolin, IBMX, BAY 60-6583, Anandamide, Dibutyryl cAMP, and Prostaglandin E2 all work through the cAMP-PKA pathway. They influence the pathway by increasing the intracellular cAMP levels, which leads to the activation of PKA. PKA then phosphorylates proteins in the TTP-αL signaling pathway, enhancing its functional activity. This class of compounds illustrates how alteration in cAMP levels can directly influence the functional activity of TTP-αL.

Other activators like A23187 and Thapsigargin act by increasing intracellular calcium levels, which can activate calcium-dependent kinases that phosphorylate proteins in the TTP-αL signaling pathway. Phorbol 12-myristate 13-acetate (PMA) and Chelerythrine chloride, on the other hand, work through the protein kinase C (PKC) pathway, either activating or inhibiting PKC to alter the phosphorylation state of proteins in the TTP-αL pathway. L-NAME acts by inhibiting nitric oxide synthase, reducing nitric oxide levels, a molecule that can inhibit PKA. Genistein the dephosphorylation of proteins in the TTP-αL pathway, maintaining their active state.

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Thapsigargin

67526-95-8sc-24017
sc-24017A
1 mg
5 mg
$136.00
$446.00
114
(2)

Thapsigargin is a non-competitive inhibitor of the SERCA pump, leading to an increase in cytosolic calcium concentration. This in turn can activate calcium-dependent kinases that phosphorylate proteins in the TTP-αL signaling pathway.