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July 26, 2011 Discovery of potent and novel S-nitrosoglutathione reductase inhibitors devoid of cytochrome P450 activities
Xicheng Sun, Jian Qiu, Sarah A. Strong, Louis S. Green, Jan W.F. Wasley, Joan P. Blonder, Dorothy B. Colagiovannia, Adam M. Stout, Sarah C. Mutka, Jane P. Richards, Gary J. Rosenthal
The pyrrole based N6022 was recently identified as a potent, selective, reversible, and efficacious S-nitrosoglutathione reductase (GSNOR) inhibitor and is currently undergoing clinical development for the treatment of acute asthma. GSNOR is a member of the alcohol dehydrogenase family (ADH) and regulates the levels of S-nitrosothiols (SNOs) through catabolism of S-nitrosoglutathione (GSNO). Reduced levels of GSNO, as well as other nitrosothiols (SNOs), have been implicated in the pathogenesis of many diseases including those of the respiratory, cardiovascular, and gastrointestinal systems. Preservation of endogenous SNOs through GSNOR inhibition presents a novel therapeutic approach with broad applicability.
We describe here the synthesis and structure–activity relationships (SAR) of novel pyrrole based analogues of N6022 focusing on removal of cytochrome P450 inhibition activities. We identified potent and novel GSNOR inhibitors having reduced CYP inhibition activities and demonstrated efficacy in a mouse ovalbumin (OVA) model of asthma.
Bioorganic & Medicinal Chemistry Letters, Volume 21, Issue 19, 1 October 2011, Pages 5849–5853 (More…Science Direct website) 
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