Synthesis of Imidazopyridines and Purines as Potent Inhibitors of Leukotriene A4 Hydrolase-Reference-Cited by-同舟云学术

Synthesis of Imidazopyridines and Purines as Potent Inhibitors of Leukotriene A4 Hydrolase

Published:2003-03 Issue:6 Volume:13 Page:1137-1139
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Penning Thomas D,Chandrakumar Nizal S,Desai Bipin N,Djuric Stevan W,Gasiecki Alan F,Malecha James W,Miyashiro Julie M,Russell Mark A,Askonas Leslie J,Gierse James K,Harding Elizabeth I,Highkin Maureen K,Kachur James F,Kim Suzanne H,Villani-Price Doreen,Pyla E.Yvonne,Ghoreishi-Haack Nayereh S,Smith Walter G

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference10 articles.

1. Inhibitors of Leukotriene A4 (LTA4) Hydrolase as Potential Anti-Inflammatory Agents>

2. Structure−Activity Relationship Studies on 1-[2-(4-Phenylphenoxy)ethyl]pyrrolidine (SC-22716), a Potent Inhibitor of Leukotriene A4 (LTA4) Hydrolase

3. Synthesis of Potent Leukotriene A4 Hydrolase Inhibitors. Identification of 3-[Methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic Acid

4. Pharmacological Characterization of SC-57461A (3-[Methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic Acid HCl), a Potent and Selective Inhibitor of Leukotriene A4Hydrolase I: In Vitro Studies

5. Pharmacological Characterization of SC-57461A (3-[Methyl[3-[4-(phenylmethyl)phenoxy]propyl]amino]propanoic Acid HCl), a Potent and Selective Inhibitor of Leukotriene A4Hydrolase II: In Vivo Studies

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