2-Iminopiperidine and Other 2-Iminoazaheterocycles as Potent Inhibitors of Human Nitric Oxide Synthase Isoforms

• Published in: Journal of medicinal chemistry 1996-02, Vol.39 (3), p.669-672
• Main Authors: Moore, William M, Webber, R. Keith, Fok, Kam F, Jerome, Gina M, Connor, Jane R, Manning, Pamela T, Wyatt, Pamela S, Misko, Thomas P, Tjoeng, Foe S, Currie, Mark G
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Bones, joints and connective tissue. Antiinflammatory agents; Enzyme Inhibitors - chemistry; Enzyme Inhibitors - pharmacology; Heterocyclic Compounds - chemistry; Heterocyclic Compounds - pharmacology; Humans; Isoenzymes - antagonists & inhibitors; Magnetic Resonance Spectroscopy; Male; Medical sciences; Nitric Oxide Synthase - antagonists & inhibitors; Pharmacology. Drug treatments; Piperidines - chemistry; Piperidines - pharmacology; Rats; Rats, Inbred Lew
• ISSN: 0022-2623; 1520-4804
• DOI: 10.1021/jm950766n

A series of 2-iminoazaheterocycles have been prepared and shown to be potent inhibitors of human nitric oxide synthase (NOS) isoforms. This series includes cyclic amidines ranging from five- to nine-membered rings, of which 2-iminopiperidine and 2-iminohomopiperidine were the most potent inhibitors, with IC50 values of 1.0 and 2.0 μM, respectively, for human inducible nitric oxide synthase. This series of cyclic inhibitors was further expanded to include analogs with heteroatoms in the 3-position of the six-membered ring. This modification was tolerated for sulfur and oxygen, but nitrogen reduced the inhibitory potency. The oral administration of 2-iminopiperidine in lipopolysaccharide (LPS)-treated rats inhibited the LPS-induced increase in plasma nitrite/nitrate levels in a dose-dependent manner, demonstrating its ability to inhibit inducible NOS activity in vivo. These cyclic amidines represent a new class of potent NOS inhibitors and the foundation for potential therapeutic agents.