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Entecavir (SQ34676) 是一种选择性 HBV 抑制剂,在 HepG2细胞中的 EC50值为3.75 nM。
Entecavir (SQ34676) 是一种选择性 HBV 抑制剂,在 HepG2细胞中的 EC50值为3.75 nM。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 178 | 现货 | |
5 mg | ¥ 413 | 现货 | |
10 mg | ¥ 588 | 现货 | |
25 mg | ¥ 980 | 现货 | |
50 mg | ¥ 1,590 | 现货 | |
100 mg | ¥ 2,680 | 现货 | |
200 mg | ¥ 3,930 | 现货 | |
500 mg | ¥ 6,220 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 433 | 现货 |
产品描述 | Entecavir (SQ34676) is a guanosine nucleoside analogue used in the treatment of chronic hepatitis B virus (HBV) infection. Entecavir therapy can be associated with flares of the underlying hepatitis B during or after therapy, but has not been linked to cases of clinically apparent liver injury. |
靶点活性 | HBV (HepG2 cells):3.75 nM(ec50) |
体外活性 | BMS-200475抑制HBV蛋白引物(EC50 值为 3.75 nM),抑制反转录酶的启动。与其他抗RNA和DNA病毒化合物相比,BMS-200475的抗病毒活性显著下降[1]。相对于其他脱氧鸟苷类似物(penciclovir、ganciclovir、lobucavir、aciclovir 或 lamivudine),BMS-200475更容易被磷酸化为其活性代谢物。BMS-200475 的细胞内半衰期为15小时[2]。 |
体内活性 | BMS-200475(p.o ,剂量自0.02至0.5 mg/kg体重,连续1至3个月治疗)能有效降低慢性感染土拨鼠中的土拨鼠乙型肝炎病毒(WHV)血症水平[3]。 |
细胞实验 | BMS 200475 is prepared in phosphate-buffered saline (PBS) and diluted with appropriate medium containing 2% fetal bovine serum. HepG2 2.2.15 cells are plated at a density of 5×105 cells per well on 12-well Biocoat collagen-coated plates and are maintained in a confluent state for 2 to 3 days before being overlaid with 1 mL of medium spiked with BMS 200475. Quantification of HBV was performed on day 10[1]. |
别名 | BMS200475, SQ34676, 恩替卡韦 |
分子量 | 277.28 |
分子式 | C12H15N5O3 |
CAS No. | 142217-69-4 |
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: 55 mg/mL (198.36 mM) | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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