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INH6 是一种有效的 Hec1 抑制剂,可选择性地破坏 Hec1/Nek2 相互作用并诱导染色体错位。它抑制HeLa 细胞生长的IC50值为2.4 μM。
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INH6 是一种有效的 Hec1 抑制剂,可选择性地破坏 Hec1/Nek2 相互作用并诱导染色体错位。它抑制HeLa 细胞生长的IC50值为2.4 μM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | ¥ 255 | 现货 | |
10 mg | ¥ 415 | 现货 | |
25 mg | ¥ 919 | 现货 | |
50 mg | ¥ 1,498 | 现货 | |
100 mg | ¥ 2,820 | 现货 | |
200 mg | ¥ 3,781 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 457 | 现货 |
产品描述 | INH6, an effective Hec1 inhibitor, selectively disrupts the Hec1/Nek2 interaction and induces chromosome mis-alignment. |
靶点活性 | NEK2:2.4 μM, Hec1:2.4 μM. |
体外活性 | INH6有效靶向Hec1/Nek2复合物进行降解,并在MDA-MB231、MDA-MB468、HeLa和K562细胞系中展现出强大的细胞杀伤活性,其IC50分别为1.7、2.1、2.4和2.5 μM。INH6还能在HeLa细胞中引发有丝分裂异常,并诱导细胞凋亡。[1] |
细胞实验 | Standard XTT assays with a four-day drug treatment procedure are performed to measure the dose-dependent cytotoxicity of INH analogs in cultured cells. Triplicate sets are measured and compiled for final data presentation. The assay is performed by using a commercial kit following the instructions. In principle, cells are plated on 96-well dishes one day before the drug treatment, followed by drug treatment on day 2 and XTT assay on day 5 after drug addition. The absorption at 595 nm is measured with a plate reader and converted to cell survival percentages in comparison to mock treated groups.(Only for Reference) |
分子量 | 322.42 |
分子式 | C19H18N2OS |
CAS No. | 1001753-24-7 |
Smiles | Cc1cc(C)c(-c2csc(NC(=O)c3ccccc3)n2)c(C)c1 |
密度 | 1.216 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||||||||||||
溶解度信息 | Ethanol: 9 mg/mL (27.9 mM) H2O: < 1 mg/mL (insoluble or slightly soluble) DMSO: 60 mg/mL (186.1 mM) | ||||||||||||||||||||||||||||||||||||||||
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