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Bcl-2-IN-23 (compound 5) 是一种选择性抑制Bcl-2的化合物。在HTB-140、HeLa和SW620细胞中,其IC50范围为25.7-33.7 μM。Bcl-2-IN-23 能与Bcl-2蛋白进行非共价竞争性结合,显著降低蛋白表达,诱导癌细胞进入晚期凋亡 (apoptosis) 和坏死 (necroptosis)。通过破坏Bcl-2介导的线粒体凋亡抑制通路,Bcl-2-IN-23 增强癌细胞对凋亡的敏感性,并减少IL-6炎症因子的释放。此化合物适用于黑色素瘤、宫颈癌及结直肠癌等恶性肿瘤的抗凋亡研究。
Bcl-2-IN-23 (compound 5) 是一种选择性抑制Bcl-2的化合物。在HTB-140、HeLa和SW620细胞中,其IC50范围为25.7-33.7 μM。Bcl-2-IN-23 能与Bcl-2蛋白进行非共价竞争性结合,显著降低蛋白表达,诱导癌细胞进入晚期凋亡 (apoptosis) 和坏死 (necroptosis)。通过破坏Bcl-2介导的线粒体凋亡抑制通路,Bcl-2-IN-23 增强癌细胞对凋亡的敏感性,并减少IL-6炎症因子的释放。此化合物适用于黑色素瘤、宫颈癌及结直肠癌等恶性肿瘤的抗凋亡研究。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 10 mg | 待询 | 待询 | |
| 50 mg | 待询 | 待询 |
Bcl-2-IN-23 相关产品
| 产品描述 | Bcl-2-IN-23 (compound 5) is a selective inhibitor targeting Bcl-2. It demonstrates an IC50 range of 25.7-33.7 μM in HTB-140, HeLa, and SW620 cells. Acting through non-covalent competitive binding to the Bcl-2 protein, Bcl-2-IN-23 significantly reduces Bcl-2 expression, inducing late-stage apoptosis and necroptosis in cancer cells. By disrupting the Bcl-2-mediated mitochondrial apoptotic inhibition pathway, it increases cancer cell susceptibility to apoptosis and reduces the release of the inflammatory factor IL-6. Bcl-2-IN-23 is applicable in anti-apoptosis research for malignant tumors such as melanoma, cervical cancer, and colorectal cancer. |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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