The class of FHL-2 inhibitors comprises a set of diverse chemicals that modulate the function of FHL-2, a protein involved in various cellular processes. These inhibitors either directly target FHL-2 or act indirectly by influencing specific signaling pathways associated with FHL-2. Galunisertib, SB431542, LY364947, SB525334, RepSox, and SD-208 are inhibitors of the transforming growth factor-beta (TGF-β) pathway by selectively targeting the TGF-β type I receptor ALK5. FHL-2 is implicated in TGF-β signaling, and these inhibitors disrupt FHL-2-mediated TGF-β signaling, affecting cellular processes such as cell proliferation, migration, and differentiation. Pirfenidone is an anti-fibrotic drug that indirectly inhibits FHL-2 by modulating TGF-β production and activity. This inhibition impacts FHL-2 involvement in cellular processes related to fibrosis and tissue remodeling.
EW-7197 is another ALK5 inhibitor that disrupts FHL-2-mediated TGF-β signaling, providing a tool to investigate the specific impact of ALK5 inhibition on FHL-2 function and cellular dynamics. SB216763 and CHIR-99021 are inhibitors of glycogen synthase kinase 3 (GSK-3), which interacts with FHL-2. These inhibitors modulate FHL-2-mediated pathways, affecting cellular processes such as proliferation and apoptosis. XAV939 and IQ-1 are inhibitors of tankyrase, indirectly influencing FHL-2-mediated pathways associated with the Wnt signaling pathway. These inhibitors impact FHL-2 involvement in cellular processes related to Wnt signaling, such as cell proliferation, migration, and differentiation. This diverse set of inhibitors provides valuable tools for researchers to explore the intricate regulatory mechanisms of FHL-2 in various cellular processes. The specific targeting of FHL-2 or its associated pathways allows for detailed investigations into the role of FHL-2 in normal cellular physiology and disease states. Researchers can leverage these inhibitors to unravel the complexities of FHL-2 function and its implications for cellular dynamics.
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