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CDK5 inhibitor 20-223, a potent inhibitor of CDK2 and CDK5, demonstrates IC50 values of 6.0 nM and 8.8 nM, respectively. It serves as an effective agent against colorectal cancer (CRC)[1].
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CDK5 inhibitor 20-223, a potent inhibitor of CDK2 and CDK5, demonstrates IC50 values of 6.0 nM and 8.8 nM, respectively. It serves as an effective agent against colorectal cancer (CRC)[1].
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
2 mg | ¥ 987 | 5日内发货 | |
5 mg | ¥ 1,740 | 5日内发货 | |
25 mg | ¥ 5,970 | 6-8周 | |
50 mg | ¥ 7,920 | 6-8周 | |
100 mg | ¥ 12,200 | 6-8周 | |
1 mL x 10 mM (in DMSO) | ¥ 1,830 | 5日内发货 |
产品描述 | CDK5 inhibitor 20-223, a potent inhibitor of CDK2 and CDK5, demonstrates IC50 values of 6.0 nM and 8.8 nM, respectively. It serves as an effective agent against colorectal cancer (CRC)[1]. |
靶点活性 | CDK2:6.0 nM (IC50), CDK5:8.8 nM (IC50) |
体外活性 | CDK5 inhibitor 20-223 (10 nM-10 μM; 72 hours) potently inhibits cell growth in a panel of colorectal cancer (CRC) cell lines[1].CDK5 inhibitor 20-223 (0.3125-20 μM; 6 hours) induces a dose-dependent decrease in pRB (S807/811) and pFAK (S732) levels in each of the three CRC cell lines[1]. Cell Viability Assay[1] Cell Line: CRC cell lines SW620, DLD1, HT29, HCT116, FET, CBS, and GEO cells |
体内活性 | CDK5 inhibitor 20-223 (8mg/kg; subcutaneously; for 14 injections) shows anti-tumor activity in human CRC xenograft tumors in nude mice[1]. Animal Model: Athymic nude mice[1] |
别名 | CDK5 inhibitor 20-223 |
分子量 | 305.37 |
分子式 | C19H19N3O |
CAS No. | 865317-30-2 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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