Abstract
α-, β- and γ-cyclodextrin-nicotinamide (α-, β- and γ-CDNA) were synthesized as NADH coenzyme models, and the binding abilities were investigated. CDNA binds a negatively charged guest stronger than unmodified cyclodextrin because of the electrostatic interaction between the nicotinamide residue and the guest molecule. Different binding abilities were measured and were dependent on cavity size.