On-bead combinatorial techniques for the identification of selective aldose reductase inhibitors.

Abstract Aldose reductase (AKR1B1; ALR2; E.C. 1.1.1.21) is an NADPH-dependent carbonyl reductase which has long been associated with complications resulting from the elevated blood glucose often found in diabetics. The development of effective inhibitors has been plagued by lack of specificity which has led to side effects in clinical trials. To address this problem, a library of bead-immobilized compounds was screened against fluorescently labeled aldose reductase in the presence of fluorescently labeled aldehyde reductase, a non-target enzyme, to identify compounds which were aldose reductase specific. Picked beads were decoded via novel bifunctional bead mass spec-based techniques and kinetic analysis of the ten inhibitors which were identified using this protocol yielded IC 50 values in the micromolar range. Most importantly, all of these compounds showed a preference for aldose reductase with selectivities as high as ∼7500-fold. The most potent of these exhibited uncompetitive inhibition versus the carbonyl-containing substrate d / l -glyceraldehyde with a K i of 1.16 μM.