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PLD-IN-1(Compound 3r),作为一种有效的磷脂酶D(phospholipase D)抑制剂,其IC50为1.97 μM,能够通过调节肺癌细胞的免疫逃避机制来抑制肿瘤。该化合物能降低CD24、CD47和PD-L1的表达,并增强钙网络蛋白的表达,从而促进巨噬细胞吞噬癌细胞。此外,PLD-IN-1抑制多种肺癌细胞线的细胞活力,包括A549、HCC44、H460和HCC15,其IC50分别为18.44、22.31、24.85和21.45 μM。它还可以诱导A549细胞凋亡(apoptosis)并抑制细胞迁移,同时增强促炎性M1巨噬细胞水平并降低抗炎性M2巨噬细胞水平,展现出在小鼠模型中的抗肿瘤活性。
PLD-IN-1(Compound 3r),作为一种有效的磷脂酶D(phospholipase D)抑制剂,其IC50为1.97 μM,能够通过调节肺癌细胞的免疫逃避机制来抑制肿瘤。该化合物能降低CD24、CD47和PD-L1的表达,并增强钙网络蛋白的表达,从而促进巨噬细胞吞噬癌细胞。此外,PLD-IN-1抑制多种肺癌细胞线的细胞活力,包括A549、HCC44、H460和HCC15,其IC50分别为18.44、22.31、24.85和21.45 μM。它还可以诱导A549细胞凋亡(apoptosis)并抑制细胞迁移,同时增强促炎性M1巨噬细胞水平并降低抗炎性M2巨噬细胞水平,展现出在小鼠模型中的抗肿瘤活性。
规格 | 价格 | 库存 | 数量 |
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10 mg | 询价 | 期货 | |
50 mg | 询价 | 期货 |
产品描述 | PLD-IN-1 (Compound 3r) is an orally effective inhibitor of phospholipase D (phospholipaseD) with an IC50 of 1.97 μM. It reduces the expression of CD24, CD47, and PD-L1 while enhancing the expression of calreticulin, thereby modulating the immune evasion mechanisms of lung cancer cells by promoting the phagocytosis of cancer cells by macrophages. PLD-IN-1 inhibits the viability of lung cancer cell lines A549, HCC44, H460, and HCC15 with IC50 values of 18.44, 22.31, 24.85, and 21.45 μM, respectively. It induces apoptosis (apoptosis) in A549 cells and inhibits cell migration. Additionally, PLD-IN-1 increases pro-inflammatory M1 macrophage levels and decreases anti-inflammatory M2 macrophage levels, exhibiting anti-tumor activity in mouse models. |
分子量 | 400.32 |
分子式 | C19H14F6N2O |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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