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Me-Indoxam
CAS No. : 172732-62-6
MCE 国际站:Me-Indoxam
产品活性:Me-Indoxam 是一种强效且细胞不渗透的分泌磷脂酶 A2 (sPLA2) 抑制剂。
研究领域:Metabolic Enzyme/Protease
作用靶点:Phospholipase
In Vitro: Me-Indoxam shows different potencies on the various sPLA2 isoforms in in vitro assays with an IC50 of less than 100 nM for hGIIA, hGIIE, and hGV; an IC50 of between 200 and 600 nM for hGIB and hGX; and an IC50 of greater than 2 mM for hGIID, hGIIF, hGIII, and hGXIIA.
Me-Indoxam is able to inhibit the activity of sPLA2s only when they are secreted in the extracellular space.
Me-Indoxam (0-10 μM; 30 min) inhibits Leukotriene C4 (LTC4) production from anti-IgE–stimulated primary human lung mast cells (HLMCs).
Me-indoxam (0.01–10 M) did not affect the basal secretion of TNF-α and IL-6 from human lung macrophages (HLM). Preincubation (15 min, 37°C) of hGX (1 μg/mL) with various concentrations of Me-indoxam before the addition to HLM dose-dependently inhibited TNF-α and IL-6 release. The IC50 values of Me-indoxam were 253±72 and 320±87 nM on TNF-α and IL-6 release, respectively.
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