Synthesis and evaluation of compounds that induce readthrough of premature termination codons

ME Jung, JM Ku, L Du, H Hu, RA Gatti

文献索引：Jung, Michael E.; Ku, Jin-Mo; Du, Liutao; Hu, Hailiang; Gatti, Richard A. Bioorganic and Medicinal Chemistry Letters, 2011 , vol. 21, # 19 p. 5842 - 5848

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被引用次数: 28

摘要

A structure–activity relationship (SAR) study was carried out to identify novel, small molecular weight compounds which induce readthrough of premature termination codons. In particular, analogs of RTC13, 1, were evaluated. In addition, hypothesizing that these compounds exhibit their activity by binding to the ribosome, we prepared the hybrid analogs 13 containing pyrimidine bases and these also showed good readthrough activity.