Date published: 2025-9-14

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TMEM131 Activators

Chemical activators of TMEM131 can engage various cellular signaling pathways to facilitate its activation. Phorbol 12-myristate 13-acetate, a well-known activator of protein kinase C (PKC), plays a pivotal role in TMEM131 activation through direct phosphorylation. PKC, once activated, targets specific serine or threonine residues on TMEM131, altering its conformation and function. Similarly, Bryostatin 1 modulates PKC, albeit through a different mechanism, ultimately leading to TMEM131 activation. Forskolin, by elevating intracellular cAMP levels, indirectly activates protein kinase A (PKA). PKA then phosphorylates TMEM131, which is a critical step for its activation. This cascade is supported by compounds such as Dibutyryl-cAMP and 8-Br-cAMP, both cAMP analogs, which directly stimulate PKA, bypassing the upstream receptors and adenylyl cyclase that are typically involved in cAMP synthesis.

Furthermore, the elevation of intracellular calcium levels is another route through which TMEM131 activation can be achieved. Ionomycin, by increasing intracellular calcium, activates calcium-dependent kinases that can target TMEM131. Thapsigargin also raises cytosolic calcium concentrations by inhibiting the SERCA pump; this calcium influx can then activate kinases that phosphorylate TMEM131. Anisomycin activates stress-activated protein kinases, which are capable of phosphorylating TMEM131, leading to its activation. Additionally, Okadaic Acid and Calyculin A inhibit protein phosphatases PP1 and PP2A, respectively. This inhibition prevents dephosphorylation of TMEM131, thereby maintaining TMEM131 in an active state. Sphingosine, after being metabolized to sphingosine-1-phosphate, activates kinases that can phosphorylate TMEM131, contributing to its activation. Lastly, Epigallocatechin gallate, by inhibiting phosphodiesterases, increases cAMP levels, further promoting PKA activation and subsequent phosphorylation of TMEM131. Through these diverse mechanisms, each chemical contributes to the activation of TMEM131 by targeting different kinases or phosphatases that directly regulate the phosphorylation state of TMEM131.

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