TY - JOUR AU - Liang, Shuobin AU - Ma, Xinyuan AU - Li, Man AU - Yi, Yanliang AU - Gao, Qianqian AU - Zhang, Yongmin AU - Zhang, Lihe AU - Zhou, Demin AU - Xiao, Sulong PY - 2022 M3 - Original Research TI - Novel β-Cyclodextrin-Based Heptavalent Glycyrrhetinic Acid Conjugates: Synthesis, Characterization, and Anti-Influenza Activity JO - Frontiers in Chemistry UR - https://www.frontiersin.org/articles/10.3389/fchem.2022.836955 VL - 10 SN - 2296-2646 N2 - In our continuing efforts toward the design of novel pentacyclic triterpene derivatives as potential anti-influenza virus entry inhibitors, a series of homogeneous heptavalent glycyrrhetinic acid derivatives based on β-cyclodextrin scaffold were designed and synthesized by click chemistry. The structure was unambiguously characterized by NMR, IR, and MALDI-TOF-MS measurements. Seven conjugates showed sufficient inhibitory activity against influenza virus infection based on the cytopathic effect reduction assay with IC50 values in the micromolar range. The interactions of conjugate 37, the most potent compound (IC50 = 2.86 μM, CC50 > 100 μM), with the influenza virus were investigated using the hemagglutination inhibition assay. Moreover, the surface plasmon resonance assay further confirmed that compound 37 bound to the influenza HA protein specifically with a dissociation constant of 5.15 × 10−7 M. Our results suggest the promising role of β-cyclodextrin as a scaffold for preparing a variety of multivalent compounds as influenza entry inhibitors. ER -