Abstract
S1P(1) receptor driven lymphopenia has proven utility in the treatment of an array of autoimmune disease states. As a part of our efforts to develop potent and selective S1P(1) receptor agonists, we have identified a novel chemical series of 4-oxo-4-(5-(5-phenyl-1,2,4-oxadiazol-3-yl)indolin-1-yl)butanoic acid S1P(1) receptor agonists.
Copyright © 2011 Elsevier Ltd. All rights reserved.
MeSH terms
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Animals
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Autoimmune Diseases / drug therapy*
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Butyrates / chemical synthesis*
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Butyrates / pharmacokinetics
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Butyrates / pharmacology*
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Disease Models, Animal
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Dogs
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Dose-Response Relationship, Drug
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Drug Discovery
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Drug Evaluation, Preclinical
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Haplorhini
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High-Throughput Screening Assays
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Humans
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Immunosuppressive Agents / chemical synthesis*
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Immunosuppressive Agents / pharmacokinetics
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Immunosuppressive Agents / pharmacology*
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Indoles / chemical synthesis*
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Indoles / pharmacokinetics
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Indoles / pharmacology*
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Lymphocytes / metabolism*
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Male
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Mice
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Mice, Inbred BALB C
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Nerve Tissue Proteins / agonists*
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Nerve Tissue Proteins / chemistry
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Oxadiazoles / chemical synthesis*
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Oxadiazoles / pharmacokinetics
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Oxadiazoles / pharmacology*
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RNA-Binding Proteins / agonists*
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RNA-Binding Proteins / chemistry
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Rats
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Rats, Sprague-Dawley
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Structure-Activity Relationship
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Substrate Specificity
Substances
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Butyrates
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GEMIN2 protein, human
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Immunosuppressive Agents
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Indoles
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Nerve Tissue Proteins
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Oxadiazoles
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RNA-Binding Proteins