Fluorescent “keep-on” type pharmacophore obtained from dynamic combinatorial library of Schiff bases

Abstract

We established a novel principle for fluorescence detection of a target protein. A low-molecular-weight fluorescent pharmacophore, as a targeted probe, was selected from a dynamic combinatorial library of Schiff bases. The pharmacophore retains its fluorescence when bound to the hydrophobic site of the target, whereas it loses it because of hydrolysis when unbound. [Figure not available: see fulltext.].