HS3ST2 activators can be classified into multiple types depending on the pathways they target to bring about HS3ST2 activation. Compounds such as Chlorate and A-769662 serve as metabolic modulators. Chlorate interrupts normal sulfate uptake, causing cells to increase HS3ST2 expression to ensure adequate sulfate conjugation. A-769662 activates AMPK, leading to an upregulation of HS3ST2 as part of cellular energy regulation. Inhibitors of key pathways also constitute another significant category. For example, LY294002 and SB203580 inhibit PI3K and p38 MAPK, respectively. Both proteins negatively regulate HS3ST2, so their inhibition results in its activation.
Forskolin and Rapamycin influence cAMP levels and mTOR signaling, respectively. Both these pathways, when modulated, can lead to HS3ST2 upregulation as part of the cellular stress response. Additionally, compounds like PD98059 and Roscovitine act by disrupting established pathways (MAPK and cell cycle regulation) and thereby push the cells to utilize HS3ST2 as part of their adaptive mechanisms. Therefore, HS3ST2 activators work through a range of biochemical pathways to modulate the protein's activity directly or indirectly.
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