Abstract
A series of novel glutarimide compounds were synthesized and their antiviral activities were evaluated. The compounds displaying the strongest antiviral activities included 5, 6f, 7e and 9 against coxsackievirus B3 (Cox B3), 10 and 6f against influenza virus A (influenza A) and 7a against herpes simplex virus 2 (HSV-2). However, most of the synthetic glutarimides showed comparatively much weaker activity against influenza A, Cox B3 and HSV-2 than the natural glutarimide compounds tested. Based on the results, it seemed likely that a conjugated system at the β-substituted moiety provides stronger antiviral activity. © 2010 Pharmaceutical Society of Japan.
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Ji, X. Y., Zhong, Z. J., Xue, S. T., Meng, S., He, W. Y., Gao, R. M., … Li, Z. R. (2010). Synthesis and antiviral activities of synthetic glutarimide derivatives. Chemical and Pharmaceutical Bulletin, 58(11), 1436–1441. https://doi.org/10.1248/cpb.58.1436
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