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保存条件 :Powder: -20°C, 3 years; 4°C, 2 years. In solvent: -80°C, 6 months; -20°C, 1 month.
库存 :货期:1-2天
供应商 :MedChemExpress LLC
CAS号 :332382-54-4
规格 :5 mg/10 mg/25 mg/50 mg
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ML-SA1
CAS No. : 332382-54-4
MCE 国际站:ML-SA1
产品活性:ML-SA1 作为一种选择性 TRPML 激动剂,通过促进溶酶体的酸化和蛋白酶活性,抑制登格病毒 2 (DENV2) 和寨卡病毒 (ZIKV)。ML-SA1 抗 DENV2 RNA 和 ZIKV RNA 的 IC50 值分别为 8.3 μM 和 52.99 μM。ML-SA1 诱发自噬。ML-SA1可用于广谱抗病毒研究。
研究领域:Membrane Transporter/Ion Channel | Neuronal Signaling | Anti-infection
作用靶点:TRP Channel | Flavivirus
In Vitro: ML-SA1 (25 μM; 0~14 hours; A549 cells) possibly affects the entry of DENV2 into host cells.
ML-SA1 (0~200 μM; A549 cells) shows that there is no cytotoxicity to the cell line observed, even at concentrations up to 200 μM. ML-SA1 (0~50 μM; A549 cells) significantly suppresses DENV2 at the RNA levels and the IC50 is 8.93 μM. ML-SA1 results in a dose-dependent decrease in ZIKV in A549 cells at both the RNA and protein levels, and the IC50 value of ML-SA1 against ZIKV RNA is 52.99 μM. ML-SA1, as an activator of TRPMLs, appears to be a potent inhibitor of DENV2 and ZIKV in vitro. ML-SA1 promotes lysosomal acidification and protease activity to inhibit viral infection. ML-SA1 can induce autophagy in Huh7 cells or A549 cells.
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