Design, synthesis, and biological testing of potential heme-coordinating nitric oxide synthase inhibitors

Abstract

Based on computer modeling of the active site of nitric oxide synthases (NOS), a series of 10 amidine compounds ( 9– 18) was designed including potential inhibitors that involve the coordination of side-chain functional groups with the iron of the heme cofactor. The most potent and selective compound was the methylthio amidine analogue 9, which was more potent than l-nitroarginine with 185-fold selectivity for inhibition of neuronal NOS over endothelial NOS. It also exhibited time-dependent inhibition, but did not involve the mechanism previously proposed for other amidine inhibitors of NOS. None of the compounds, however, exhibited heme-binding characteristics according to absorption spectroscopy.