兴奋剂
化学
1-磷酸鞘氨醇
鞘氨醇-1-磷酸受体
受体
鞘氨醇
药理学
生物化学
生物
作者
Petr Váchal,Leslie M. Toth,Jeffrey J. Hale,Lin Yan,Sander G. Mills,Gary Chrebet,Carol A. Koehane,Richard Hajdu,James A. Milligan,Mark Rosenbach,Suzanne Mandala
标识
DOI:10.1016/j.bmcl.2006.04.064
摘要
Novel series of sphingosine-1-phosphate (S1P) receptor agonists were developed through a systematic SAR aimed to achieve high selectivity for a single member of the S1P family of receptors, S1P1. The optimized structure represents a highly S1P1-selective and efficacious agonist: S1P1/S1P2, S1P1/S1P3, S1P1/S1P4 > 10,000-fold, S1P1/S1P5 > 600-fold, while EC50 (S1P1) <0.2 nM. In vivo experiments are consistent with S1P1 receptor agonism alone being sufficient for achieving desired lymphocyte-lowering effect.
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