Date published: 2025-10-11

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LRFN1 Inhibitors

Chemical inhibitors of LRFN1 can achieve their inhibitory action through interference with the protein kinase C (PKC) pathway. LRFN1 function at synapses is regulated by its phosphorylation state, which can be influenced by PKC activity. Phorbol 12-myristate 13-acetate (PMA), which activates PKC, can lead to the phosphorylation of LRFN1, promoting its internalization away from the cell membrane where it cannot execute its synaptic roles. Conversely, Staurosporine, a well-known PKC inhibitor, can prevent this phosphorylation, thereby inhibiting the functional activity of LRFN1. Similarly, Bisindolylmaleimide I targets PKC to avert LRFN1 phosphorylation and subsequent internalization that would otherwise lead to its functional inhibition. The chemical Gö 6983, another potent PKC inhibitor, can reduce LRFN1 inhibition by halting PKC-mediated regulatory processes essential for LRFN1's synaptic function.

Further, Ro-31-8220, as a PKC inhibitor, can prevent the phosphorylation-dependent endocytosis of LRFN1, preserving its synaptic presence and function. Gö 6976, with selectivity for Ca2+-dependent PKC isoforms, can impede phosphorylation mechanisms that would culminate in LRFN1 inhibition. LY333531, or Ruboxistaurin, selectively impedes PKCβ, thus potentially disrupting PKCβ-driven LRFN1 phosphorylation. Another inhibitor, Chelerythrine chloride, can also block PKC activity, preventing LRFN1 phosphorylation and subsequent functional inhibition. Calphostin C, Hispidin, and Balanol, all serving as PKC inhibitors, can similarly mitigate PKC-dependent phosphorylation of LRFN1, ensuring its synaptic functionality is maintained. Lastly, Sotrastaurin targets PKC to prevent phosphorylation that would otherwise lead to the functional inhibition of LRFN1, ensuring that the protein remains active within its synaptic role. Each of these chemicals, through their targeted inhibition of PKC, can maintain LRFN1 functionality by avoiding the phosphorylation and internalization that serve as regulatory mechanisms for LRFN1's synaptic activity.

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