C(4)-alkyl substituted furanyl cyclobutenediones as potent, orally bioavailable CXCR2 and CXCR1 receptor antagonists-Reference-Cited by-同舟云学术

C(4)-alkyl substituted furanyl cyclobutenediones as potent, orally bioavailable CXCR2 and CXCR1 receptor antagonists

Published:2007-07 Issue:13 Volume:17 Page:3778-3783
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Chao Jianhua,Taveras Arthur G.,Chao Jianping,Aki Cynthia,Dwyer Michael,Yu Younong,Purakkattle Biju,Rindgen Diane,Jakway James,Hipkin William,Fosetta James,Fan Xuedong,Lundell Daniel,Fine Jay,Minnicozzi Michael,Phillips Jonathan,Merritt J. Robert

Publisher

Elsevier BV

Subject

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

Reference33 articles.

1. Structure and Functional Expression of a Human Interleukin-8 Receptor

2. Cloning of Complementary DNA Encoding a Functional Human Interleukin-8 Receptor

3. Elevated Levels of NAP-1/Interleukin-8 Are Present in the Airspaces of Patients with the Adult Respiratory Distress Syndrome and Are Associated with Increased Mortality

4. The Role of CXCR2/CXCR2 Ligands in Acute Lung Injury

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