5-Fluorinated l-Lysine Analogues as Selective Induced Nitric Oxide Synthase Inhibitors-Reference-Cited by-同舟云学术

5-Fluorinated l-Lysine Analogues as Selective Induced Nitric Oxide Synthase Inhibitors

Published:2004-01-13 Issue:4 Volume:47 Page:900-906
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Hallinan E. Ann¹,Hagen Timothy J.¹,Bergmanis Arija¹,Moore William M.¹,Jerome Gina M.¹,Spangler Dale P.¹,Stevens Anna M.¹,Shieh Huey S.¹,Manning Pamela T.¹,Pitzele Barnett S.¹

Affiliation:

1. Pfizer, 4901 Searle Parkway, Skokie, Illinois 60077, Pfizer, 800 North Lindbergh Boulevard, St. Louis, Missouri 63167, and Pfizer, 700 Chesterfield Parkway, St. Louis, Missiouri 63198

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm030348f

Reference19 articles.

1. INHIBITION OF NITRIC OXIDE SYNTHASE AS A POTENTIAL THERAPEUTIC TARGET

2. L-N6-(1-Iminoethyl)lysine: A Selective Inhibitor of Inducible Nitric Oxide Synthase

3. 2-Iminopiperidine and Other 2-Iminoazaheterocycles as Potent Inhibitors of Human Nitric Oxide Synthase Isoforms

4. Nitric oxide: a key mediator in the early and late phase of carrageenan-induced rat paw inflammation

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