Pirodavir (Synonyms: 吡罗达韦; R77975)
目录号: PL03713 纯度: ≥99%
CAS No. :124436-59-5
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中文名称
Pirodavir
中文别名
吡罗达韦;Pirodavir 抑制剂;无中文名;4-[2-[1-(6-甲基-3-哒嗪基)-4-哌啶基]乙氧基]苯甲酸乙酯
英文名称
Pirodavir
英文别名
Benzoic acid,4-[2-[1-(6-methyl-3-pyridazinyl)-4-piperidinyl]ethoxy]-, ethyl ester;ethyl 4-[2-[1-(6-methylpyridazin-3-yl)piperidin-4-yl]ethoxy]benzoate;(METHYLPYRIDAZINE PIPERIDINE ETHYLOXYPHENYL)ETHYLACETATE;Benzoic acid,4-(2-(1-(6-methyl-3-pyridazinyl)-4-piperidinyl)ethoxy)-,ethyl ester;ethyl 4-(2-(1-(6-methylpyridazin-3-yl)piperidin-4-yl)ethoxy)benzoate;Pirodavirum;R-77975;4-[2-[1-(6-Methyl-3-pyridazinyl)-4-piperidinyl]ethoxy]-benzoic acid ethyl ester;Ethyl 4-[2-[1-(6-methyl-3-pyridazinyl)-4-piperidinyl]ethoxy]benzoate;R77,975;4-[2-[1-(6-Methyl-3-pyridazinyl)-4-piperidinyl]ethoxy]benzoic Acid Ethyl Ester;pirodavi;pirodavir;R 77975, Pirodavir;pirodavir(R 77975);ethyl p-(2-(1-(6-Methyl-3-pyridazinyl)-4-piperidyl)ethoxy) benzoate;R 77975;R77975;Pirodavir, >=99%
Cas No.
124436-59-5
分子式
C21H27N3O3
分子量
369.46
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Pirodavir 是一种有效的小核糖核酸病毒抑制剂,高效作用于 A 和 B 型鼻病毒(rhinovirus)。Pirodavir 非常有效作用于病毒产量减少试验,IC90 为 2.3 nM。
生物活性
Pirodavir is a potent, broad-spectrum picornavirus inhibitor, and is highly active against both group A and group B rhinovirus serotypes. Pirodavir is very potent in a virus yield reduction assay (IC 90 =2.3 nM).
性状
Solid
IC50 & Target[1][2]
Rhinovirus
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 IC50 of 5,420 nM and an IC90 of >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. 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 c
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Barnard DL, et al. In vitro activity of expanded-spectrum pyridazinyl oxime ethers related to pirodavir: novel capsid-binding inhibitors with potent antipicornavirus activity. Antimicrob Agents Chemother. 2004 May;48(5):1766-72.
[2]. Andries K, et al. In vitro activity of pirodavir (R 77975), a substituted phenoxy-pyridazinamine with broad-spectrum antipicornaviralactivity. Antimicrob Agents Chemother. 1992 Jan;36(1):100-7.
溶解度数据
In Vitro: DMSO : 10 mg/mL (27.07 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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