Date published: 2025-9-11

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UNKL Activators

Forskolin raises cAMP levels, leading to the activation of PKA, which may enhance UNKL activity through subsequent phosphorylation events. In contrast, LY294002 and U0126 serve as inhibitors to the PI3K and MEK1/2 enzymes, respectively, altering pivotal pathways such as AKT and MAPK/ERK, thereby possibly affecting the regulatory mechanisms of UNKL. SB203580 and SP600125, by targeting p38 MAP kinase and JNK, respectively, mediate alterations in the cellular response to stress, potentially impacting UNKL's functional role in such processes.

Similarly, rapamycin acts on the mTOR pathway, which is integral to protein synthesis and autophagy, processes that can intersect with UNKL's activity. The proteasome inhibitor MG132 may stabilize proteins that interact with or modulate UNKL, indirectly influencing its function. Sodium Orthovanadate, a phosphatase inhibitor, may affect UNKL by enhancing kinase signaling pathways. ER stress inducers like thapsigargin and tunicamycin could activate stress response pathways that involve UNKL, while 2-Deoxy-D-glucose simulates glucose deprivation, activating stress responses that may intersect with UNKL's role in the cell.

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