Kelley J L, Selway J W, Schaeffer H J
J Pharm Sci. 1985 Dec;74(12):1302-4. doi: 10.1002/jps.2600741211.
Several acyclic puromycin analogues containing hydrocarbon substituents on the 1'-position of the aminoethoxymethyl moiety were synthesized and tested for antiviral activity. The N-carbobenzoxy intermediate 7c was active in vitro against Mengo and Semliki Forest viruses.
合成了几种在氨基乙氧基甲基部分的1'-位含有烃取代基的无环嘌呤霉素类似物,并测试了它们的抗病毒活性。N-苄氧羰基中间体7c在体外对门戈病毒和塞姆利基森林病毒具有活性。