Date published: 2025-9-20

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2610021K21Rik Inhibitors

The chemical class described as potential Efcab11 Inhibitors encompasses a variety of compounds that primarily target calcium signaling pathways. These chemicals can modulate the availability of intracellular calcium, which is essential for the function of EF-hand calcium-binding domains like Efcab11. The modulating effect of these chemicals on calcium levels can result in the alteration of Efcab11's calcium-binding ability and consequently its activity.

Calcium channel blockers such as verapamil, nifedipine, diltiazem, amlodipine, and bepridil can inhibit the influx of calcium from the extracellular space into the cytosol. By reducing intracellular calcium concentration, these chemicals can decrease the activation of calcium-dependent proteins, including Efcab11. Thapsigargin and TMB-8 disrupt the calcium stores within the endoplasmic reticulum, further influencing calcium-dependent signaling and Efcab11's potential interaction with calcium. 2-APB, ryanodine, and SKF-96365 interfere with the release and regulation of calcium within the cell, which can alter the function of Efcab11. BAPTA, being a calcium chelator, can sequester calcium ions and decrease their bioavailability, thereby potentially inhibiting the activity of calcium-binding proteins like Efcab11. Gadolinium chloride's inhibition of stretch-activated channels also contributes to the modulation of calcium signaling, which can impact Efcab11's role in cellular processes.

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