SAR studies of 3-arylpropionic acids as potent and selective agonists of sphingosine-1-phosphate receptor-1 (S1P1) with enhanced pharmacokinetic properties-Reference-Cited by-同舟云学术

SAR studies of 3-arylpropionic acids as potent and selective agonists of sphingosine-1-phosphate receptor-1 (S1P1) with enhanced pharmacokinetic properties

Published:2007-02 Issue:3 Volume:17 Page:828-831
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Yan Lin,Huo Pei,Hale Jeffrey J.,Mills Sander G.,Hajdu Richard,Keohane Carol A.,Rosenbach Mark J.,Milligan James A.,Shei Gan-Ju,Chrebet Gary,Bergstrom James,Card Deborah,Mandala Suzanne M.

Publisher

Elsevier BV

Subject

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

Reference12 articles.

1. FTY720: Sphingosine 1-Phosphate Receptor-1 in the Control of Lymphocyte Egress and Endothelial Barrier Function

2. Alteration of Lymphocyte Trafficking by Sphingosine-1-Phosphate Receptor Agonists

3. The Immune Modulator FTY720 Targets Sphingosine 1-Phosphate Receptors

4. FTY720: early clinical experience

5. Discovery of 3-arylpropionic acids as potent agonists of sphingosine-1-phosphate receptor-1 (S1P1) with high selectivity against all other known S1P receptor subtypes

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