Date published: 2025-10-29

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LZTFL1 Activators

LZTFL1 Activators are a set of compounds that enhance the activity of LZTFL1 through various intracellular signaling pathways, primarily involving the modulation of cyclic nucleotide levels. Forskolin, IBMX, Rolipram, and Vinpocetine elevate intracellular levels of cAMP, which could activate protein kinase A (PKA) and subsequently influence cellular functions where LZTFL1 is a factor, such as the assembly and function of cilia and signaling cascades. In a similar vein, compounds like SildenafilL. ZTFL1 Activators comprise a range of chemical compounds that indirectly influence the functional activity of LZTFL1 by modulating distinct cellular signaling pathways. Compounds such as Forskolin, IBMX, Rolipram, and Vinpocetine heighten intracellular cAMP levels, potentially activating protein kinase A (PKA). The activation of PKA may lead to phosphorylation events that indirectly enhance LZTFL1's regulatory functions in cellular processes, particularly those related to ciliary structure and function, which are critical for signal transduction. Similarly, Sildenafil, Zaprinast, and YC-1, by inhibiting phosphodiesterase 5 (PDE5) and increasing cGMP levels, could elevate LZTFL1 activity through cGMP-dependent protein kinase (PKG) signaling pathways, impacting LZTFL1's role in cellular homeostasis. The use of 8-Br-cAMP, a cAMP analog, also suggests a direct PKA-mediated enhancement of LZTFL1 activity through phosphorylation of downstream substrates that may interact with LZTFL1.

Furthermore, AICAR and Metformin, activators of AMP-activated protein kinase (AMPK), could indirectly heighten LZTFL1 activity by modulating energy balance and metabolic signaling pathways, potentially intersecting LZTFL1's function. The precursor to nitric oxide, L-Arginine, may enhance LZTFL1 activity by initiating cGMP pathway signaling, thus impacting LZTFL1's involvement in cellular signaling, especially within endothelial cells. Dipyridamole, a compound that augments both cAMP and cGMP levels, could similarly bolster LZTFL1 activity via dual cAMP/cGMP-dependent signaling pathways. Collectively, these LZTFL1 Activators, through their targeted effects on cyclic nucleotide signaling, facilitate the enhancement of LZTFL1-related functions which are pivotal in cellular signaling and homeostasis.

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