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PI3K/AKT-IN-4 (compound 3) 是源自Salvia castaneaDiels f根和根茎的二萜类化合物。这种化合物展现出显著的抗肿瘤活性,它通过阻断Hep3B细胞在G0/G1期的细胞周期、诱导线粒体功能障碍和氧化应激,从而抑制肝细胞癌细胞的活力及增殖(IC50=4.72 μM),并推动细胞凋亡 (apoptosis)。PI3K/AKT-IN-4 还能通过抑制PI3K-Akt信号通路并针对PARP1和CDK2靶点,进一步抑制肿瘤细胞生长。
PI3K/AKT-IN-4 (compound 3) 是源自Salvia castaneaDiels f根和根茎的二萜类化合物。这种化合物展现出显著的抗肿瘤活性,它通过阻断Hep3B细胞在G0/G1期的细胞周期、诱导线粒体功能障碍和氧化应激,从而抑制肝细胞癌细胞的活力及增殖(IC50=4.72 μM),并推动细胞凋亡 (apoptosis)。PI3K/AKT-IN-4 还能通过抑制PI3K-Akt信号通路并针对PARP1和CDK2靶点,进一步抑制肿瘤细胞生长。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
10 mg | 询价 | 期货 | |
50 mg | 询价 | 期货 |
产品描述 | PI3K/AKT-IN-4 (compound 3), a diterpenoid extracted from the roots and rhizomes of Salvia castanea Dielsf., exhibits antitumor properties by inhibiting cell viability and proliferation (IC 50 =4.72 μM) and promoting apoptosis in Hep3B cells. This compound obstructs the G0/G1 phase of the cell cycle, triggers mitochondrial dysfunction, and induces oxidative stress. Moreover, PI3K/AKT-IN-4 combats hepatocellular carcinoma through the inhibition of the PI3K-Akt signaling pathway and by interacting with PARP1 and CDK2 targets. |
分子量 | 286.41 |
分子式 | C19H26O2 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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