Journal
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
Volume 14, Issue 13, Pages 3501-3505Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2004.04.070
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Structurally modified 3-(N-benzylamino)propylphosphonic acid SIP receptor agonists that maintain affinity for S1P(1), and have decreased affinity for S1P(3) are efficacious, but exhibit decreased acute cardiovascular toxicity in rodents than do nonselective agonists. (C) 2004 Elsevier Ltd. All rights reserved.
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