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KS176是选择性高活性乳腺癌耐药蛋白多药转运通道抑制剂,在Pheo A 和Hoechst 检测中,IC50值分别为0.59和1.39 μM。
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KS176是选择性高活性乳腺癌耐药蛋白多药转运通道抑制剂,在Pheo A 和Hoechst 检测中,IC50值分别为0.59和1.39 μM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 167 | 现货 | |
2 mg | ¥ 238 | 现货 | |
5 mg | ¥ 443 | 现货 | |
10 mg | ¥ 738 | 现货 | |
25 mg | ¥ 1,570 | 现货 | |
50 mg | ¥ 2,370 | 现货 | |
100 mg | ¥ 3,450 | 现货 | |
200 mg | ¥ 4,780 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 443 | 现货 |
产品描述 | KS176 is a potent and selective inhibitor of the breast cancer resistance protein (BCRP) multidrug transporter, showing no inhibitory activity against P-gp or MRP1. |
靶点活性 | BCRP(Pheo A):0.59 μM |
激酶实验 | Phospholipase D activity is quantified using our established method of measuring the formation of [32P]-radiolabeled PBt. Cellular lipids are extracted and PBt is isolated using our published methods of lipid extraction and thin layer chromatographic separation, respectively. Radioactivity is measured using liquid scintillation counting and quantified as DPM normalized to 106 counts in the total cellular lipid extract or as percentage of control (vehicle-treated cells). |
分子量 | 405.4 |
分子式 | C22H19N3O5 |
CAS No. | 1253452-78-6 |
Smiles | OCCc1ccc(NC(=O)c2ccccc2NC(=O)c2ccc(cc2)[N+]([O-])=O)cc1 |
密度 | 1.401 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 | DMSO: 55 mg/mL (135.67 mM) | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
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