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LQZ-7I is a small-molecule survivin-targeting inhibitor that disrupts survivin dimerization, induces proteasome-mediated survivin degradation, and has demonstrated oral antitumor activity in xenograft models. It is supplied as a high-purity solid with documented solubility and storage conditions for use in cellular and in vivo oncology research.
Inhibits survivin dimerization and promotes survivin degradation.
Demonstrates oral efficacy in xenograft tumor models.
High reported purity suitable for research applications.
Soluble in DMSO; in vivo formulation protocols available.
Available in multiple small pack sizes for preclinical studies.
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MS-444 is a small-molecule inhibitor of myosin light chain kinase (MLCK) used in research to probe MLCK-dependent signaling and cytoskeletal regulation. It inhibits purified smooth muscle MLCK with an IC50 of 10 μM and is supplied as a solid or as a 10 mM solution in DMSO.
Inhibits MLCK with an IC50 of 10 μM.
High purity, approximately 99.5%.
Available as solid and as 10 mM solution in DMSO.
Molecular weight 230.22 g/mol; formula C13H10O4.
Stored protected from light; suitable for biochemical and cell-based research.
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