Forskolin is a potent adenylyl cyclase activator that raises cAMP levels, thereby enhancing protein kinase A (PKA) activity. PKA is a key regulatory enzyme that can phosphorylate a breadth of substrates, possibly including or affecting those associated with SAMD14. PMA is a robust activator of protein kinase C (PKC), a kinase group that modifies the function of proteins through phosphorylation, and could thereby alter proteins that are linked to the regulation of SAMD14. Ionomycin, a calcium ionophore, raises intracellular calcium levels, activating calcium-dependent signaling pathways. These pathways can have a significant impact on cellular processes and proteins that may be associated with SAMD14. PD98059 and U0126, both MEK inhibitors, can result in the attenuation or alteration of the MAPK/ERK pathway, potentially leading to the indirect enhancement of SAMD14 activity through compensatory cellular mechanisms.
LY294002, a PI3K inhibitor, affects the AKT signaling pathway, which is a critical regulator of many cellular functions, and may influence the regulatory network surrounding SAMD14. Other compounds include A23187, another calcium ionophore, which, like Ionomycin, can modulate calcium-mediated signaling pathways. SB203580 and SP600125, inhibitors of p38 MAPK and JNK respectively, alter their specific kinase pathways and may indirectly upregulate SAMD14 activity through complex signaling feedback loops. KN-93, which inhibits CaMKII, along with Y-27632, a ROCK inhibitor, and Bisindolylmaleimide I, a specific PKC inhibitor, all serve to adjust the phosphorylation landscape within the cell, potentially impacting proteins that regulate or interact with SAMD14.
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