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Alsterpaullone 是高效的 CDK 抑制剂,是一种 ATP 竞争性的 GSK-3alpha/GSK-3beta 抑制剂,且作用的 IC50值都为 4 nM。它有用于神经退行性和增生性疾病的研究潜力,具有抗肿瘤活性,诱导白血病细胞凋亡。
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Alsterpaullone 是高效的 CDK 抑制剂,是一种 ATP 竞争性的 GSK-3alpha/GSK-3beta 抑制剂,且作用的 IC50值都为 4 nM。它有用于神经退行性和增生性疾病的研究潜力,具有抗肿瘤活性,诱导白血病细胞凋亡。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 460 | 现货 | |
5 mg | ¥ 1,090 | 现货 | |
10 mg | ¥ 1,730 | 现货 | |
25 mg | ¥ 2,970 | 现货 | |
50 mg | ¥ 4,170 | 现货 | |
100 mg | ¥ 5,620 | 现货 | |
200 mg | ¥ 7,560 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 1,000 | 现货 |
产品描述 | Alsterpaullone is a Cyclin-Dependent Kinase Inhibitor, Mediated Toxicity in HeLa Cells Through Apoptosis-Inducing Effec |
靶点活性 | CDK1-CyclinB:35 nM, K2/Cyc E:200 nM, CDK5-p35:40 nM, CDK2-CyclinA:15 nMCD |
体外活性 | Alsterpaullone inhibited HeLa cells in a time-dependent (0-72 h) and dose-dependent (0-30 μ M) manner.?In the presence of alsterpaullone, HeLa cells were arrested in G2/M prior to undergoing apoptosis via a mechanism that is involved in the regulation of various antiapoptotic genes, DNA-repair, transcription, and cell cycle progression.?Compared to controls, alsterpaullone effectively prevented HeLa cells from entering S-phase.?These potential therapeutic efficacies could be correlated with the activation of caspase-3[1]. |
分子量 | 293.28 |
分子式 | C16H11N3O3 |
CAS No. | 237430-03-4 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||
溶解度信息 | DMSO: 12 mg/mL (40.92 mM) | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
DMSO
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