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                同义名:
                    
                        
                            
                                SCH-48973; V-073
                            
                        
                    
                
                
                
                    
                     
                    
                     
                
            
Pocapavir (SCH-48973)是一种口服有效的衣壳抑制剂,可防止病毒粒子在进入细胞后进行脱壳。它对脊髓灰质炎病毒具有抗病毒活性,也可抑制肠病毒的感染。
 
                                 
                                
                            

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| 描述 | Pocapavir, also known as SCH-48973, is an orally active capsid inhibitor. Pocapavir prevents viruses from entering cells and then unencapsulating them. Pocapavir has antiviral activity against poliovirus and also inhibits enteroviral infections[1].Pocapavir belongs to a group of picornavirus antiviral mechanisms that prevent viral replication by preventing viral uncoating and release of viral RNA into cells[2]. | 
| Concentration | Treated Time | Description | References | |
| BGMK cells | 0.02 to 0.11 µg/ml | 18 to 24 hours | To evaluate the inhibitory effect of SCH 48973 on echoviruses, results showed significant antiviral activity. | Antimicrob Agents Chemother. 1997 Jun;41(6):1220-5 | 
| HeLa cells | 0.02 to 0.11 µg/ml | 18 to 24 hours | To evaluate the inhibitory effect of SCH 48973 on the cytopathic effect of five picornaviruses, results showed significant antiviral activity with no cytotoxicity. | Antimicrob Agents Chemother. 1997 Jun;41(6):1220-5 | 
| RD cells | 0.9 µg/ml | 2 to 3 days | To assess the antiviral spectrum of SCH 48973 against various enteroviruses, results showed inhibition against 80% of the virus strains. | Antimicrob Agents Chemother. 1997 Jun;41(6):1220-5 | 
| Administration | Dosage | Frequency | Description | References | ||
| Mice | Mouse poliovirus model | Oral | 3 to 20 mg/kg/day | Three times daily for 21 days | To evaluate the therapeutic efficacy of SCH 48973 in a mouse poliovirus model, results showed significant improvement in survival and reduction in brain viral titers. | Antimicrob Agents Chemother. 1997 Jun;41(6):1220-5 | 
| 计算器 | ||||
| 存储液制备 |  | 1mg | 5mg | 10mg | 
| 1 mM 5 mM 10 mM | 2.36mL 0.47mL 0.24mL | 11.80mL 2.36mL 1.18mL | 23.60mL 4.72mL 2.36mL | |
| CAS号 | 146949-21-5 | 
| 分子式 | C21H17Cl3O3 | 
| 分子量 | 423.72 | 
| SMILES Code | COC1=CC=C(OCC2=CC=C(C=C2)COC3=C(Cl)C=CC=C3Cl)C(Cl)=C1 | 
| MDL No. | MFCD00950032 | 
| 别名 | SCH-48973; V-073; V074 | 
| 运输 | 蓝冰 | 
| 存储条件 | In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C | 
| 溶解方案 | DMSO: 105 mg/mL(247.81 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 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶 
 
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