CAS NO: | 124436-59-5 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
2mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | Pirodavir is a potent, broad-spectrum picornavirus inhibitor, and is highly active against both group A and group Brhinovirusserotypes. Pirodavir is very potent in a virus yield reduction assay (IC90=2.3 nM). | ||||||||||||||||
IC50& Target | Rhinovirus[1] | ||||||||||||||||
体外研究 (In Vitro) | Pirodavir is a potent, broad-spectrum picornavirus inhibitor. Pirodavir inhibits 80 of the 100 human rhinovirus (HRV) strains tested at a concentration of 64 ng/mL. In that same study, Pirodavir is also effective in inhibiting 16 enteroviruses, with a mean 80% inhibitory concentration (IC80) of 1,300 ng/mL. Pirodavir inhibits enterovirus 71 replication with an IC50of 5,420 nM and an IC90of >13,350 nM. Pirodavir inhibits 56 rhinovirus laboratory strains and three of the clinical isolates tested. Pirodavir inhibits 59% of the serotypes and isolates with IC50s of<100 nm[1]. Pirodavir concentrations of 16 and 4μg/mL reduces cell growth by 66% (s.e.m. 0.75) and 28% (s.e.m. 0.25), respectively. Lower concentrations (1μg/mL) of Pirodavir are not inhibitory for cell growth. The 50% cytotoxic concentration of pirodavir for logarithmic cell growth at 37℃ is 7μg/mL. Under the conditions of the antiviral assay (confluent HeLa cells at 33℃), the 50% cytotoxic concentration is >50μg/mL[2]. | ||||||||||||||||
分子量 | 369.46 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C21H27N3O3 | ||||||||||||||||
CAS 号 | 124436-59-5 | ||||||||||||||||
中文名称 | 吡罗达韦 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 10 mg/mL(27.07 mM;Need ultrasonic) 配制储备液
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