1. Synthesis and bioevaluation of water-soluble β -cyclodextrin-diterpene acid conjugates.
- Author
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LiWen H, Yanliang Y, Tretyakova EV, Smirnova AA, Kazakova OB, and Xiao S
- Abstract
A series of β -cyclodextrin ( β -CD)-conjugates were prepared by combining three abietane-type diterpene acids with two azide-functionalized β -CDs via click chemistry, and the antiviral activity against wild-type and omicron SARS-CoV-2 spike pseudovirus as well as the antibacterial activity against Escherichia coli were investigated. All the synthesised conjugates exhibited no significant cytotoxicity to BHK-21-hACE2 cells with cell viability over 80% at concentration of 15 µ M. Among the conjugates, the heptavalent β -CD-dehydroabietic acid conjugate 6b exhibited higher anti-SARS-CoV-2 activity against the omicron variant compared to the other conjugates. This study suggested that the multivalent diterpene acid derivatives may have potential application against coronaviruses as entry inhibitors.
- Published
- 2024
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