MIZIP Inhibitors primarily target the RhoA/ROCK/SRF signaling cascade, given MIZIP's function in repressing myocardin, a key coactivator of SRF. By targeting this pathway, the inhibitors can modulate the influence of MIZIP on SRF-responsive genes. Compounds like CCG-1423 and CCG-203971 directly inhibit RhoA-induced SRF-mediated transcription, which makes them particularly pertinent to MIZIP's indirect regulatory effects via myocardin. Additionally, ROCK inhibitors such as Y-27632 and H-1152 further demonstrate the interconnectedness of the Rho/ROCK/SRF pathway.
The significance of actin dynamics and myosin interaction becomes apparent with the inclusion of actin modulators like Cytochalasin D, Jasplakinolide, and Latrunculin A. These compounds influence actin polymerization and depolymerization, with direct ramifications for SRF-responsive genes, which are closely associated with actin dynamics. This intricately woven system showcases the necessity of actin-myosin modulators, including Blebbistatin and ML-7. Rho-specific regulators like NSC 23766 further bolster the potential list of MIZIP modulators. While the Wnt pathway inhibitors, Wnt-C59 and FH535, were incorporated due to the known crosstalk with Rho/ROCK signaling, they signify the intricacy and interconnectedness of cellular pathways.
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