Date published: 2025-9-12

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hnRNP A3 Activators

hnRNP A3 activators can operate through a myriad of pathways, pivoting primarily on their modulation of RNA processing, transcription, and translation. Key players in this realm, such as Forskolin and Resveratrol, wield their influence by reshaping cAMP levels and activating sirtuins, respectively, to impact the functionality of RNA binding proteins, including hnRNP A3. Actinomycin D, by directly intervening with RNA synthesis, and Sodium Butyrate, by altering chromatin architecture, hold the potential to recalibrate the activity of hnRNP A3 in the sphere of mRNA processing and transport.

In the proteostasis landscape, compounds like MG-132 alter protein turnover dynamics, presenting the potential for a reshaped hnRNP A3 activity profile. The realm of splicing is not untouched, with compounds like Spliceostatin A and Pladienolide B, both of which could modify the engagement of hnRNP A3 within the spliceosomal machinery. DRB, by virtue of its action on RNA polymerase II, along with Oxaliplatin, which impacts DNA dynamics, can alter the role of hnRNP A3 in mRNA processing. Agents such as Caffeine, with broad signaling impacts, Staurosporine, a kinase inhibitor, and Ivermectin, influencing nuclear transport, all represent potential pivot points for modulating hnRNP A3's RNA binding and shuttling dynamics.

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