Selecting against S1P3 enhances the acute cardiovascular tolerability of 3-(N-benzyl)aminopropylphosphonic acid S1P receptor agonists
摘要:
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.