Date published: 2026-6-10

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MARK Inhibitors

Santa Cruz Biotechnology now offers a broad range of MARK Inhibitors for use in various applications. MARK Inhibitors are a significant category of chemical compounds known for their role in modulating the activity of Microtubule Affinity-Regulating Kinase (MARK). These kinases are critical regulators of microtubule dynamics, influencing various cellular processes such as mitosis, cell motility, and neuronal signaling. In scientific research, MARK Inhibitors are invaluable for studying the intricate mechanisms of cell structure and function, particularly in the context of cytoskeletal organization. Researchers utilize these inhibitors to dissect the pathways that govern microtubule stability and to explore the broader implications of MARK activity in cellular physiology. This category of chemicals has been instrumental in advancing our understanding of cellular architecture and the molecular underpinnings of cell cycle regulation. By selectively inhibiting MARK enzymes, scientists can investigate the specific roles these kinases play in various biological systems, leading to insights that have far-reaching implications in fields such as developmental biology, neurobiology, and cancer research. MARK Inhibitors thus serve as powerful tools in the scientific community, enabling detailed exploration of cellular processes at the molecular level. View detailed information on our available MARK Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

10Z-Hymenialdisine

82005-12-7sc-360987
500 µg
$210.00
(1)

10Z-Hymenialdisine exhibits unique reactivity as an acid halide, characterized by its ability to form stable acyl derivatives through nucleophilic acyl substitution. This compound demonstrates selective reactivity with amines and alcohols, leading to the formation of diverse esters and amides. Its distinct steric and electronic properties influence reaction kinetics, allowing for rapid transformations under mild conditions, which can be harnessed in synthetic pathways to create complex molecular architectures.