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描述 | Besifovir (LB80331), transformed from LB80380, undergoes further metabolic conversion to its active derivative, LB80317. It is identified as an innovative, orally administered antiviral compound effective against the hepatitis B virus (HBV)[1].[2]. |
体内研究 | LB80380, acting as a prodrug, is efficiently absorbed when taken orally (doses of 30, 60, 120, 240 mg), transforming into its parent compound, Besifovir (LB80331), with LB80380 remaining undetectable in the bloodstream. The peak times (Tmaxs) for LB80331 are observed between 1.0 and 2.0 hours after ingestion, followed by a monoexponential decline in plasma concentration of LB80331, with half-life (t1/2) averages ranging from 2.5 to 3.3 hours[2]. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
3.34mL 0.67mL 0.33mL |
16.71mL 3.34mL 1.67mL |
33.42mL 6.68mL 3.34mL |
CAS号 | 441785-25-7 |
分子式 | C10H14N5O4P |
分子量 | 299.223 |
别名 | LB80331 |
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,Sealed in dry,2-8°C |
溶解度 |
DMSO: 250 mg/mL(835.5 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 H2O: 100 mg/mL(334.2 mM) |
动物实验配方 |