Date published: 2025-9-17

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Rabr Activators

Rabr Activators are chemical compounds that indirectly enhance the functional activity of Rabr by influencing various signaling pathways. Forskolin and IBMX both act to increase intracellular cAMP levels, with Forskolin directly activating adenylyl cyclase and IBMX inhibiting phosphodiesterases, leading to the activation of PKA. This kinase can phosphorylate proteins in signaling pathways that Rabr is a part of, thereby enhancing its activity. PMA, through its activation of PKC, and Epigallocatechin gallate, as a kinase inhibitor, indirectly contribute to Rabr activation by modifying phosphorylation patterns of proteins within Rabr-related pathways. PI3K inhibitors like LY294002 and Wortmannin disrupt downstream signaling which may enhance Rabr function by impacting related signaling cascades, particularly those associated with membrane dynamics.

The Rabr functional activity is also influenced by compounds that modulate MAPK and calcium signaling. U0126 and SB203580, which inhibit MEK1/2 and p38 MAPK respectively, can shift the signaling balance towards Rabr-involved pathways, thereby enhancing its activity. Genistein reduces tyrosine kinase signaling, potentially allowing Rabr pathways to be more active. Calcium modulators such as A23187 and Thapsigargin elevate intracellular calcium levels, which could activate calcium-dependent processes that indirectly enhance Rabr activity. Lastly, Sphingosine-1-phosphate acts on G protein-coupled receptors to influence signaling pathways that could involve Rabr, thus contributing to its functional enhancement in processes like cell growth and trafficking. These Rabr Activators, through their targeted biochemical effects, collectively facilitate the enhancement of Rabr-mediated functions within the cell.

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