Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10591955 | Bioorganic & Medicinal Chemistry Letters | 2013 | 4 Pages |
Abstract
The anti hepatitis C virus (HCV) activity of (+)-lycoricidine (1) was evaluated for the first time in this letter, yielding an EC50 value of 0.55Â nmol/mL and an selection index (SI) value of 12.72. Further studies indicated that 1 induced this effect by down-regulating host heat-stress cognate 70 (Hsc70) expression. In addition, 20 derivatives were designed and synthesised to investigate the basic structure-activity relationship (SAR) of the title compound. Several of these derivatives exhibit a good inhibition of HCV, such as compound 3 (EC50Â =Â 0.68Â nmol/mL, SIÂ =Â 33.86), compound 2d (EC50Â =Â 15Â nmol/mL, SIÂ =Â 12) and compound 5 (EC50Â =Â 33Â nmol/mL, SI >10.91). Meanwhile, the experimental data suggest that the modification of certain groups of (+)-lycoricidine can reduce the cytotoxicity of the compounds.
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Authors
Duo-Zhi Chen, Jian-Dong Jiang, Ke-Qing Zhang, Hong-Ping He, Ying-Tong Di, Yu Zhang, Jie-Yun Cai, Lei Wang, Shun-Lin Li, Ping Yi, Zong-Gen Peng, Xiao-Jiang Hao,