Date published: 2026-6-6

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Arg Inhibitors

Santa Cruz Biotechnology now offers a broad range of Arg Inhibitors for use in various applications. Arg inhibitors target the Abelson-related gene (Arg) kinase, a non-receptor tyrosine kinase that plays a critical role in regulating the actin cytoskeleton, cell adhesion, and signal transduction pathways involved in cellular growth and differentiation. These inhibitors are vital tools in scientific research, particularly for studying the molecular mechanisms underlying cell movement, morphogenesis, and the cellular response to external stimuli. By inhibiting Arg kinase activity, researchers can explore its role in various cellular processes, such as the regulation of cytoskeletal dynamics, which is crucial for maintaining cell shape and enabling cell migration. Arg inhibitors are also employed in studies focused on understanding how this kinase interacts with other signaling molecules to coordinate complex cellular behaviors, including the formation of cellular protrusions like lamellipodia and filopodia. In the context of cancer research, these inhibitors are used to investigate the contribution of Arg kinase to tumor cell invasion and metastasis, providing insights into how the modulation of cytoskeletal organization influences the metastatic potential of cancer cells. Additionally, Arg inhibitors are valuable in neurobiology, where they help explain the kinase's role in neural development and synaptic plasticity. The availability of a diverse range of Arg inhibitors allows scientists to design experiments tailored to specific aspects of Arg kinase function, advancing our understanding of its involvement in both normal cellular processes and pathological conditions. View detailed information on our available Arg Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

N-Desmethyl Imatinib

404844-02-6sc-208027
500 µg
$398.00
4
(1)

N-Desmethyl Imatinib exhibits unique properties as an arg, characterized by its ability to interact with specific protein targets through hydrogen bonding and hydrophobic interactions. This compound influences cellular signaling by modulating the activity of key kinases, thereby affecting downstream pathways. Its kinetic profile reveals a rapid association and dissociation with target proteins, highlighting its potential to alter cellular responses and regulatory mechanisms. The compound's distinct physicochemical properties enhance its reactivity in various biochemical environments.

VEGFR2 Kinase Inhibitor III

204005-46-9sc-202851
5 mg
$165.00
7
(1)

VEGFR2 Kinase Inhibitor III demonstrates distinctive characteristics as an arg, particularly through its selective binding affinity for VEGFR2, which is mediated by intricate electrostatic interactions and conformational changes in the target protein. This compound exhibits a unique reaction kinetics profile, allowing for prolonged engagement with its target, thereby influencing angiogenic signaling pathways. Its solubility and stability in diverse conditions further enhance its reactivity, making it a notable entity in biochemical studies.