Synthesis and biological evaluation of N-mercaptoacylcysteine derivatives as leukotriene A4 hydrolase inhibitors-Reference-Cited by-同舟云学术

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Synthesis and biological evaluation of N-mercaptoacylcysteine derivatives as leukotriene A4 hydrolase inhibitors

Published:2009-01 Issue:2 Volume:19 Page:442-446
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Enomoto Hiroshi,Morikawa Yuko,Miyake Yurika,Tsuji Fumio,Mizuchi Maki,Suhara Hiroshi,Fujimura Ken-ichi,Horiuchi Masato,Ban Masakazu

Publisher

Elsevier BV

Subject

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

Reference21 articles.

1. Leukotriene A4 Hydrolase/Aminopeptidase, the Gatekeeper of Chemotactic Leukotriene B4 Biosynthesis

2. Leukotriene B, a potent chemokinetic and aggregating substance released from polymorphonuclear leukocytes

3. Lipoxygenation of arachidonic acid as a source of polymorphonuclear leukocyte chemotactic factors in synovial fluid and tissue in rheumatoid arthritis and spondyloarthritis.

4. Significance of Leukotriene-A4 Hydrolase in the Pathogenesis of Psoriasis

5. Enhanced Synthesis of Leukotriene B4 by Colonic Mucosa in Inflammatory Bowel Disease

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Protecting Groups in Peptide Synthesis;Methods in Molecular Biology;2019-12-27

2. A remarkable activity of human leukotriene A4 hydrolase (LTA4H) toward unnatural amino acids;Amino Acids;2014-02-27

3. Chemically triggered C-ON bond homolysis in alkoxyamines. Part 7. Remote polar effect;Journal of Physical Organic Chemistry;2014-01-29

4. Development of predictive quantitative structure–activity relationship model and its application in the discovery of human leukotriene A4 hydrolase inhibitors;Future Medicinal Chemistry;2013-01

5. Visible light-mediated oxidative decarboxylation of arylacetic acids into benzyl radicals: addition to electron-deficient alkenes by using photoredox catalysts;Chemical Communications;2013

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