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CAS No. : 1713240-67-5
MCE 国际站:Zegocractin
产品活性:Zegocractin (CM-4620) 是一种钙离子释放激活通道 (CRAC channel) 的抑制剂,其对 Orai1/STIM1 和 Orai2/STIM1 的 IC50 值分别为 119 nM 和 895 nM。
研究领域:Membrane Transporter/Ion Channel
作用靶点:CRAC Channel
In Vitro: It is determined that Zegocractin (compound 1) inhibits Orai 1/STIM1 channels with an IC50 of 119 nM, and Orai2/STIM1 channels with an IC50 of 895 nM. It is more potent on Orai1 than Orai2-type CRAC channels. In human PBMCs, Zegocractin potently inhibits release of multiple cytokines which play important roles in T cells (IC50s, IFN γ: 138 nM, IL-4: 879 nM, IL-6: 135 nM, IL-1β: 240 nM, IL-10: 303 nM, TNFα: 225 nM, IL-2: 59 nM, IL-17 120 nM).
In Vivo: Mouse PACs are treated with CRAC inhibitors Zegocractin or GSK-7975A and monitored for their rate of Calcium uptake. Both CRAC inhibitors reduce the rate of store-operated Calcium entry into the ER to 50% of controllevels upon treatment with 700 nM of inhibitor. Zegocractin blocks 100% of reuptake at 10 mM.
相关产品:Drug Repurposing Compound Library Plus | Clinical Compound Library Plus | Bioactive Compound Library Plus | Membrane Transporter/Ion Channel Compound Library | Clinical Compound Library | Drug Repurposing Compound Library | Pyroptosis Compound Library | Mechanoreceptors Compound Library | Targeted Diversity Library | Protein-protein Interaction Inhibitor Library | Non-steroidal Anti-Inflammatory Compound Library | Membrane Protein-targeted Compound Library | Membrane Receptor-targeted Compound Library | MRS1845 | RO2959 hydrochloride | SOCE inhibitor 1 | SKF-96365 hydrochloride | GSK-5498A | CRAC intermediate 1 | GSK-5503A | 5J-4 | Synta66 | CRAC intermediate 2 | YM-58483 | piCRAC-1 | Tanshinone IIA sulfonate sodium
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货号: HY-101942
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