法匹拉韦 T6833
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
50 mg | 259793-96-9 | ¥2,890.00 | 询底价 |
1 mL | 259793-96-9 | ¥728.00 | 询底价 |
500 mg | 259793-96-9 | ¥8,890.00 | 询底价 |
100 mg | 259793-96-9 | ¥3,990.00 | 询底价 |
5 mg | 259793-96-9 | ¥659.00 | 询底价 |
10 mg | 259793-96-9 | ¥1,177.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Favipiravir
描述: Favipiravir (T-705) 是一种有效且选择性的 RNA 依赖性 RNA 聚合酶抑制剂,用于治疗流感病毒感染。
细胞实验: The cytotoxicity of T-705 is evaluated by an assay with XTT. XTT is converted to aqueous formazan by an enzyme in MDCK cells, Vero cells, HEL cells, A549 cells, HeLa cells, and HEp-2 cells. The compounds are diluted to the appropriate concentrations (volume, 100 μl) with test medium (EMEM containing 10% FCS) in 96-well culture plates in which each well contains a concentration of 2 × 103 cells/100 μL. The test plates are incubated for 3 days at 37°C in 100% humidity and 5% CO2. After 3 days, 50 μl of the XTT reagent (1 mg/ml in FCS-free EMEM containing 5 mM phenazine methosulfate) is added, and the reaction product is assayed by measurement of the absorbance at 450 nm with a microplate reader. Cytotoxicity is expressed as the 50% cell-inhibitory concentration (CC50).(Only for Reference)
体外活性: Favipiravir shows anti-influenza virus activities with IC50 ranged from 0.013 to 0.48 μg/ml for the influenza A viruses, from 0.039 to 0.089 μg/ml for the influenza B viruses, and from 0.030 to 0.057 μg/ml for the influenza C viruses. In mammalian cell lines (MDCK cells, Vero cells, HEL cells, A549 cells, HeLa cells, and HEp-2 cells), Favipiravir shows no cytotoxicity at concentrations up to 1,000 μg/ml. [1] In MDCK cells inoculated with seasonal influenza A (H1N1) viruses, Favipiravir induces lethal mutagenesis. [2]
体内活性: In influenza virus-infected mice, Favipiravir (200 mg/kg/day, p.o.) protects the mice from death from influenza virus infection. [1] In mice experimentally infected with Ebola virus, Favipiravir efficiently blocks viral production, reaching an antiviral effectiveness of 95% and 99.6% at 2 and 6days after initiation of treatment, respectively. [3]
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: Ethanol : 12 mg/mL(76.4 mM)
H2O : 5 mg/mL (31.82 mM)
DMSO : 45 mg/mL (286.44 mM)
关键字: SARS-CoV | DNA/RNA Synthesis | Influenza Virus | inhibit | T705 | SARS coronavirus | Inhibitor | T 705 | Favipiravir
相关产品: Z795161988 | Atazanavir sulfate | SARS-CoV-2-IN-45 | Lopinavir | PF-00835231 | SARS-CoV-2-IN-42 | Silymarin | NSC89641 | Ritonavir | FOY 251
相关库: Drug Repurposing Compound Library | Approved Drug Library | Anti-Cancer Drug Library | Clinical Compound Library | Bioactive Compounds Library Max | Human Metabolite Library | Inhibitor Library | Anti-Cancer Clinical Compound Library | Anti-Cancer Approved Drug Library | DNA Damage & Repair Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途