Date published: 2026-5-3

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L-type Ca++ CP α 1S Inhibitors

Santa Cruz Biotechnology now offers a broad range of L-type Ca++ CP α 1S Inhibitors for use in various applications. These inhibitors are designed to target the L-type calcium channels, particularly focusing on the alpha 1S subunit. This subunit is essential for the regulation of calcium influx into cells, which plays a pivotal role in numerous cellular processes such as muscle contraction, neurotransmitter release, and gene expression regulation. In the scientific community, L-type Ca++ CP α 1S Inhibitors are invaluable tools for investigating the intricate roles of calcium channels in cellular signaling and their interactions with various cellular pathways. Researchers employ these inhibitors to identify new regulatory mechanisms and potential targets for further study, providing insights into the fundamental processes of cellular regulation and adaptation. Additionally, these inhibitors are utilized in high-throughput screening assays to discover novel modulators of calcium channel activity, facilitating the development of experimental models that delve into the complex signaling networks involving calcium dynamics. By offering precise control over calcium channel activity, these inhibitors enable comprehensive studies of calcium's impact on cellular physiology and its broader implications across diverse biological contexts. View detailed information on our available L-type Ca++ CP α 1S Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Barnidipine HCl

104757-53-1sc-357293B
sc-357293A
sc-357293
10 mg
1 g
100 mg
$20.00
$417.00
$124.00
(1)

Barnidipine HCl functions as a selective inhibitor of L-type calcium channels, specifically targeting the alpha 1S subunit. Its unique molecular architecture allows for precise interactions with channel binding sites, modulating calcium ion flux. The compound's stereochemistry plays a crucial role in its binding affinity, influencing the kinetics of channel inhibition. Furthermore, its solubility characteristics and ionization state can affect its distribution and interaction with cellular membranes, impacting its overall efficacy in modulating calcium signaling pathways.