Synthesis and evaluation of acridine-and acridone-based anti-herpes agents with topoisomerase activity

…, AA Madhok, H Hiasa, DM Ferguson

文献索引：Goodell, John R.; Madhok, Avni A.; Hiasa, Hiroshi; Ferguson, David M. Bioorganic and Medicinal Chemistry, 2006 , vol. 14, # 16 p. 5467 - 5480

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被引用次数: 108

摘要

The discovery of new non-nucleoside antiviral compounds is of significant and growing interest for treating herpes virus infections due to the emergence of nucleoside-resistant strains. Using a whole cell virus-induced cytopathogenic assay, we tested a series of substituted triaryl heterocyclic compounds including acridones, xanthones, and acridines. The compounds which showed activity against Herpes Simplex-1 and/or Herpes Simplex- ...