Date published: 2025-9-14

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LRRC70 Inhibitors

Chemical inhibitors of LRRC70 can interact with signaling pathways that are crucial for its function. For instance, SB-431542, LY-364947, and SD-208 are chemicals which specifically target the transforming growth factor-beta (TGF-beta) signaling pathway. TGF-beta is known to regulate various cellular processes and by inhibiting this pathway, these chemicals can reduce the activation of proteins involved in this signaling cascade, including LRRC70. The inhibition occurs through the blockade of TGF-beta type I receptor known as activin receptor-like kinase 5 (ALK5), and possibly ALK4, which are integral to the propagation of the TGF-beta signal. By binding to these receptors and preventing their phosphorylation and subsequent signaling, these inhibitors can attenuate the functional activity of LRRC70.

Further inhibition can be achieved by employing chemicals like A-83-01, GW788388, and RepSox, which also target ALK5 and related receptors. By maintaining a selective inhibition profile, these chemicals ensure that the signaling associated with LRRC70 is specifically dampened. In a similar vein, Galunisertib (LY-2157299) and EW-7197 restrict the kinase activity of TGF-beta receptors, thereby reducing the downstream signaling events that lead to LRRC70 activation. ITD-1's role in selectively inhibiting the TGF-beta pathway further supports the inhibition of LRRC70, as it decreases the pathway's overall activity. LY2109761, with its dual inhibition of both TGF-beta receptor types I and II, provides a broad mechanism by which the activity of LRRC70 can be reduced. Lastly, SB-505124 and SB-525334, by inhibiting ALK5, contribute to the functional inhibition of LRRC70 by preventing the initiation of the signaling cascade that would normally lead to its activation. These chemical inhibitors, while diverse in their structure, share the common goal of disrupting the TGF-beta signaling pathway at various points, thereby inhibiting the functional activity of LRRC70.

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