The chemical class identified as AATK Activators comprises various compounds that interact with cellular signaling pathways and processes relevant to the function of Apoptosis-Associated Tyrosine Kinase (AATK). This diverse collection includes naturally occurring substances like polyphenols, flavonoids, and other plant-derived compounds. These substances are recognized for their roles in modulating kinase activities and influencing apoptotic signaling, thereby having an impact on the activity of AATK. Members such as Epigallocatechin gallate (EGCG), Resveratrol, and Quercetin are particularly notable for their interaction with kinase pathways and apoptotic processes, which are central to AATK's role in cellular processes like neuronal differentiation and apoptosis. Curcumin, another significant component of this class, is known for its broad-spectrum influence on signaling pathways, encompassing those related to apoptosis and kinase activity, thus affecting AATK.
Additionally, the AATK Activators class includes compounds like Silymarin, Genistein, and Kaempferol, which exert effects on cellular stress responses and kinase signaling pathways. Agents such as Sulforaphane and Vitamin E (Tocopherol) are considered for their capability to modulate cellular stress responses and oxidative stress pathways, potentially altering AATK activity. Zinc Sulfate is included due to its role in kinase activity and cellular signaling, reflective of zinc ions' importance in biological processes. Naringenin and Piperine, with their capacity to modulate various cellular signaling pathways, represent further avenues through which AATK activity can be influenced. This chemical class, therefore, represents a comprehensive array of compounds, each playing a role in the complex network of cellular signaling and the modulation of kinase activities. These compounds provide insight into the regulation of a key kinase involved in essential cellular functions, underscoring the intricate nature of cellular regulation and the possibility of specific protein activity modulation through various signaling pathways.
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