作者:Lowell D. Markley、Yulan C. Tong、Jacqueline K. Dulworth、David L. Steward、Christopher T. Goralski、Howard Johnston、Steven G. Wood、Anna P. Vinogradoff、Thomas M. Bargar
DOI:10.1021/jm00153a020
日期:1986.3
Phenoxybenzenes and phenoxypyridines were prepared and tested for the effect of substituents on antipicornavirus activity. The most active compound, 2-(3,4-dichlorophenoxy)-5-nitrobenzonitrile (8), demonstrated broad-spectrum antipicornavirus activity. Compound 8 and several analogues each given orally prior to and during infection protected mice against an otherwise lethal challenge with coxsackievirus
制备苯氧基苯和苯氧基吡啶,并测试取代基对抗小核糖核酸病毒活性的影响。最具活性的化合物2-(3,4-二氯苯氧基)-5-硝基苯甲腈(8)具有广谱抗幽门螺杆菌活性。分别在感染前和感染期间口服给予的化合物8和几种类似物可保护小鼠免受柯萨奇病毒A21致命的攻击。