RBM25 activators are a class of chemicals that can indirectly enhance the function of the RNA-binding protein RBM25. These chemicals impact various signaling pathways or cellular processes that RBM25 is involved in, thereby influencing its activity. For instance, Anisomycin, a protein synthesis inhibitor, triggers the JNK and p38 MAPK pathways, which RBM25 is associated with, leading to enhanced functionality of RBM25. Thapsigargin, another RBM25 activator, is a potent inhibitor of SERCA and induces ER stress, activating the unfolded protein response pathway and hence indirectly enhancing the function of RBM25.
Another compound, Rapamycin, an mTOR inhibitor, indirectly influences RBM25 by impacting cellular growth and proliferation pathways. Forskolin, an activator of adenylate cyclase, increases the level of cAMP, regulating several physiological responses. Given that RBM25 is implicated in cAMP-dependent signaling pathways, Forskolin indirectly boosts the function of RBM25. Furthermore, Resveratrol, a natural polyphenol, activates Sirtuin 1, an enzyme associated with cellular stress response, indirectly enhancing RBM25 function. Genistein, a tyrosine kinase inhibitor, can influence the PI3K/Akt pathway, where RBM25 operates, thereby indirectly enhancing RBM25 functionality. Staurosporine, a potent protein kinase inhibitor, indirectly enhances RBM25 by modifying protein kinase signaling. Trichostatin A, a histone deacetylase inhibitor, by altering the acetylation state of histones, influences the expression of downstream genes including RBM25, thereby indirectly enhancing its function. LY294002, a potent PI3K inhibitor, indirectly enhances the function of RBM25 by inhibiting PI3K, a pathway in which RBM25 operates. PD98059, an inhibitor of MEK, can indirectly enhance the function of RBM25 by inhibiting MEK in the MAPK pathway. Y-27632, a selective inhibitor of Rho-associated protein kinases (ROCKs), indirectly enhances the function of RBM25 by modifying protein kinase signaling. Lastly, SB203580, a potent inhibitor of p38 MAPK, indirectly enhances the function of RBM25 by inhibiting p38 MAPK, a pathway in which RBM25 operates.
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