Bemnifosbuvir是一种具有口服活性的 HCV 病毒复制抑制剂,对 SARS-CoV-2 (COVID-19) 感染的 EC90 为 0.47 μM,并展现全基因型抗病毒活性。
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Type | HazMat fee for 500 gram (Estimated) |
Excepted Quantity | USD 0.00 |
Limited Quantity | USD 15-60 |
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描述 | Bemnifosbuvir (AT-511) is a potent orally active HCV viral replication inhibitor effective against SARS-CoV-2 (COVID-19) infection in vitro (EC90=0.47 μM), exhibiting pangenotypic antiviral activity [1][2][3]. |
体内研究 | Orally administered to rats (500 mg/kg) and monkeys (30 mg/kg, 100 mg/kg, or 300 mg/kg), Bemnifosbuvir preferentially delivers high levels of AT-9010 in the liverin vivo[1]. |
体外研究 | Bemnifosbuvir demonstrates pan-genotypic antiviral activity, inhibiting HCV genotype 1a (HCV GT1a), HCV GT1b, HCV GT2a, HCV GT3a, HCV GT4a, and HCV GT5a replication with EC50 values of 12.8 nM, 12.5 nM, 9.2 nM, 10.3 nM, 14.7 nM, and 28.5 nM, respectively [1]. In normal human airway epithelial cells, the concentration of Bemnifosbuvir required to inhibit replication of SARS-CoV-2 by EC90 is 0.47 μM, similar to its EC90 against HCoV-229E, HCoV-OC43, and SARS-CoV in Huh-7 cells [2]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.72mL 0.34mL 0.17mL |
8.60mL 1.72mL 0.86mL |
17.20mL 3.44mL 1.72mL |
CAS号 | 1998705-64-8 |
分子式 | C24H33FN7O7P |
分子量 | 581.534 |
别名 | AT-511 |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
溶解度 |
DMSO: 190 mg/mL(326.72 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |