The inhibitors of BMP2KL function through various mechanisms to dampen the signaling and downstream effects that this protein mediates. One class of these inhibitors targets the BMP type I receptors, such as ALK2 and ALK3, which are integral to the BMP2KL signaling pathway. By selectively inhibiting these receptors' kinase activity, these compounds effectively reduce the signaling cascade that leads to BMP2KL's role in cellular differentiation processes. Another inhibitor acts by directly targeting the Smad1 phosphorylation, a key event in BMP2KL signaling. This inhibition disrupts the transcriptional regulation and gene expression that BMP2KL typically influences, culminating in a reduction of its biological activities.
Furthermore, some inhibitors function by impeding the activity of TGF-β superfamily receptors that are upstream of BMP2KL, thus indirectly diminishing its signaling potential. These inhibitors, while not directly targeting BMP2KL, exploit the interconnected nature of cellular pathways to decrease the functional activity of BMP2KL by inhibiting related signaling events. Additionally, there are inhibitors that influence the cell cycle and cytoskeletal dynamics, which are not the direct functions of BMP2KL but are essential for the proper execution of the processes in which BMP2KL is a critical player.
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