前药
体内
体外
化学
三嗪
病毒学
甲型流感病毒
病毒
生物
生物化学
遗传学
高分子化学
作者
Kevin J. Sparrow,Rinu Shrestha,James M. Wood,Keith Clinch,Brett L. Hurst,Hong Wang,Brian B. Gowen,Justin G. Julander,E. Bart Tarbet,Alice M. McSweeney,Vernon K. Ward,Gary B. Evans,Lawrence D. Harris
标识
DOI:10.1021/acsmedchemlett.3c00048
摘要
We report for the first time the antiviral activities of two iminovirs (antiviral imino-C-nucleosides) 1 and 2, structurally related to galidesivir (Immucillin A, BCX4430). An iminovir containing the 4-aminopyrrolo[2,1-f][1,2,4-triazine] nucleobase found in remdesivir exhibited submicromolar inhibition of multiple strains of influenza A and B viruses, as well as members of the Bunyavirales order. We also report the first syntheses of ProTide prodrugs of iminovir monophosphates, which unexpectedly displayed poorer viral inhibition than their parent nucleosides in vitro. An efficient synthesis of the 4-aminopyrrolo[2,1-f][1,2,4-triazine]-containing iminovir 2 was developed to enable preliminary in vivo studies, wherein it displayed significant toxicity in BALB/c mice and limited protection against influenza. Further modification of this anti-influenza iminovir will therefore be required to improve its therapeutic value.
科研通智能强力驱动
Strongly Powered by AbleSci AI