Development of CXCR3 antagonists. Part 4: Discovery of 2-amino-(4-tropinyl)quinolines-Reference-Cited by-同舟云学术

Development of CXCR3 antagonists. Part 4: Discovery of 2-amino-(4-tropinyl)quinolines

Published:2008-01 Issue:2 Volume:18 Page:629-633
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Knight Roland L.,Allen Daniel R.,Birch Helen L.,Chapman Gayle A.,Galvin Frances C.,Jopling Louise A.,Lock Christopher J.,Meissner Johannes W.G.,Owen David A.,Raphy Gilles,Watson Robert J.,Williams Sophie C.

Publisher

Elsevier BV

Subject

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

Reference16 articles.

1. CXCR3-binding Chemokines: Novel Multifunctional Therapeutic Targets

2. Targeting the Function of IFN-γ-Inducible Protein 10 Suppresses Ongoing Adjuvant Arthritis

3. Inhibition of IFN-γ-Inducible Protein-10 Abrogates Colitis in IL-10−/−Mice

4. Genetic deletion of chemokine receptor CXCR3 or antibody blockade of its ligand IP-10 modulates posttransplantation graft-site lymphocytic infiltrates and prolongs functional graft survival in pancreatic islet allograft recipients

5. Requirement of the Chemokine Receptor CXCR3 for Acute Allograft Rejection

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