Beilstein J. Org. Chem.2009,5, No. 28, doi:10.3762/bjoc.5.28
useful nNOS-selective inhibitors is a difficult task as the substrate for all three isoforms is L-arginine, and so they have similar activesites. In recent years, we have developed several potent and highly selective inhibitors of nNOS that have solved this problem by exploiting subtle differences among
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Graphical Abstract
Figure 1:
Lead compounds 1 and 2; 2- and 4-aminothiazole analogs 3 and 4a-c.