Abstract

The pharmacological properties of a cyclomaltoheptaose (β-cyclodextrin) series of adamantane-group-bearing compounds that exhibit potent antibacterial activity have been studied, both isolated and in complex with β-cyclodextrins (βCDs). In this work, the structure of the bromide salt of 2-(3-dimethylaminopropyl)tricyclo[3.3.1.1 3,7]decan-2-ol (ADM-10) complexed with βCD and ten water molecules was studied in the solid state by X-ray crystallography and in solution by NMR spectroscopy. X-ray crystallographic studies of the complex were performed both at room and cryogenic temperatures. The long aliphatic chain of ADM-10 adopts a single conformation at low temperature in contrast to what is observed at room temperature, where two side chain conformations are seen. Both NMR and X-ray crystallography studies indicate that the adamantane moiety of ADM-10 is buried in the βCD cavity. Chemical shifts in NMR experiments can be explained on the basis of the crystal structure of the complex.

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