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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 | In stock | |
| 5 mg | ¥ 1,090 | In stock | |
| 10 mg | ¥ 1,730 | In stock | |
| 25 mg | ¥ 2,970 | In stock | |
| 50 mg | ¥ 4,170 | In stock | |
| 100 mg | ¥ 5,620 | In stock | |
| 200 mg | ¥ 7,560 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,000 | In stock |
ALSTERPAULLONE 相关产品
| 产品描述 | Alsterpaullone is a Cyclin-Dependent Kinase Inhibitor, Mediated Toxicity in HeLa Cells Through Apoptosis-Inducing Effec |
| 靶点活性 | CDK2-CyclinA:15 nMCD, CDK5-p35:40 nM, CDK1-CyclinB:35 nM, K2/Cyc E:200 nM, GSK-3β:4 nM, GSK-3α:4 |
| 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 |
| Smiles | [O-][N+](=O)c1ccc2[nH]c-3c(CC(=O)Nc4ccccc-34)c2c1 |
| 密度 | 1.461 g/cm3 (Predicted) |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||
| 溶解度信息 | DMSO: 12 mg/mL (40.92 mM), Sonication is recommended. | |||||||||||||||||||||||||
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