Date published: 2025-9-17

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LRRC37B Inhibitors

LRRC37B inhibitor compounds like W-7 Hydrochloride, Thapsigargin, Ionomycin, and BAPTA-AM can alter calcium signaling by either antagonizing calmodulin, inhibiting calcium ATPases, increasing intracellular calcium levels, or chelating calcium ions, respectively. Since calcium signaling is pivotal in various cellular processes, these inhibitors can affect the function of proteins like LRRC37B that may be regulated by calcium. The class would also include inhibitors of major intracellular signaling cascades such as LY294002 for PI3K/Akt, Cyclosporin A for calcineurin, JNK Inhibitor VIII for the JNK pathway, SB 203580 for p38 MAPK, and U73122 for phospholipase C. Each of these inhibitors is designed to interfere with specific signaling events that, while not directly inhibiting LRRC37B, could alter the cellular context in which LRRC37B operates.

MG-132 would represent the proteostasis affecting members of this class. By inhibiting the proteasome, MG-132 can lead to an accumulation of proteins within the cell, potentially affecting the turnover or stability of LRRC37B. Collectively, these inhibitors, though not directly targeting LRRC37B, would exert their effects on the regulatory mechanisms and signaling pathways that control the cellular functions in which LRRC37B might be implicated. They would influence the activity of LRRC37B by altering the cellular processes that govern protein activity, stability, and interaction networks.

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