摘要
Five optically active dibenzylbutyrolactone lignans were synthesized through a lipase-catalyzed transesterification route and evaluated for their inhibitory activity against HIV-1 replication in acutely infected H9 cells. Compounds 1 and 2 demonstrated anti-HIV replication activity with an EC50 values of 2.2 and 0.16 μg/ml and a therapeutic index values of 9.1 and 5, respectively. Structure-antiviral activity relationships are discussed.
原文 | 英語 |
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頁(從 - 到) | 941-944 |
頁數 | 4 |
期刊 | Bioorganic and Medicinal Chemistry Letters |
卷 | 6 |
發行號 | 8 |
DOIs | |
出版狀態 | 已發佈 - 4月 23 1996 |
ASJC Scopus subject areas
- 藥物發現
- 分子醫學
- 分子生物學
- 生物化學
- 臨床生物化學
- 藥學科學
- 有機化學