Synthesis and antiviral activities of synthetic glutarimide derivatives.
Xing-yue Ji, Zhao-jin Zhong, Si-tu Xue, Shuai Meng, Wei-ying He, Rong-mei Gao, Yu-huan Li, Zhuo-rong Li
Index: Chem. Pharm. Bull. 58(11) , 1436-41, (2010)
Full Text: HTML
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.
Related Compounds
Related Articles:
2014-12-16
[Biochemistry 53(49) , 7854-65, (2014)]
2005-08-31
[J. Am. Chem. Soc. 127(34) , 11930-1, (2005)]
Enantiomerization mechanism of thalidomide and the role of water and hydroxide ions.
2012-11-05
[Chemistry 18(45) , 14305-13, (2012)]
2008-11-15
[Bioorg. Med. Chem. Lett. 18(22) , 5951-4, (2008)]
2011-09-01
[Inflamm. Res. 60(9) , 879-88, (2011)]