Date published: 2025-9-12

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SNAPC 50 Activators

SNAPC50 Activators encompass a range of chemical compounds that, through their distinct actions on various cellular signaling pathways, indirectly enhance the functional activity of SNAPC50, particularly in transcription regulation. Forskolin, by elevating cAMP levels, indirectly augments SNAPC50's role in transcription, as elevated cAMP affects transcription factors that could influence SNAPC50-mediated processes. Genistein and Sphingosine-1-phosphate, through tyrosine kinase inhibition and lipid signaling modulation respectively, also contribute to enhancing SNAPC50's functional role. They achieve this by shifting the balance of cellular signaling towards pathways where SNAPC50 is active, thus indirectly promoting its involvement in transcription regulation. Thapsigargin and A23187, by increasing intracellular calcium levels, affect calcium-dependent signaling pathways. This modulation can lead to the enhancement of SNAPC50's activity in transcription regulation, as calcium-sensitive transcription factors play a crucial role in these processes.

Further, the functional activity of SNAPC50 is influenced by compounds like Phorbol 12-myristate 13-acetate (PMA), LY294002, Wortmannin, SB203580, U0126, Staurosporine, and Epigallocatechin Gallate (EGCG), each contributing uniquely to its activation. PMA, through PKC activation, LY294002, and Wortmannin, as PI3K inhibitors, along with SB203580 and U0126 affecting the MAPK pathway, all indirectly enhance SNAPC50's role in transcription regulation by influencing key signaling pathways that intersect with transcriptional control. Staurosporine, a broad-spectrum kinase inhibitor, and EGCG, known for its multi-kinase inhibition property, further contribute to this enhancement by modulating kinase-dependent transcription pathways. Collectively, these SNAPC50 Activators, through their targeted effects on cellular signaling, facilitate the indirect enhancement of SNAPC50-mediated functions in transcription regulation, highlighting the intricate interplay between various signaling cascades and transcriptional control mechanisms.

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