Sphingosine-
1
-phosphate analogs that are potent, and selective agonists at one or more S1P receptors, specifically the S1P
1
receptor type are provided. The disclosed compounds include an optional phosphate moiety as well as compounds with hydrolysis-resistant phosphate surrogates such as phosphonates, alpha-substituted phosphonates, and phosphothionates.
本发明提供了一种有效且选择性地作用于一个或多个S1P受体,特别是S1P1受体类型的
鞘氨醇-1-
磷酸类似物。所述化合物包括一个可选的
磷酸酯基团,以及具有抗
水解的
磷酸酯替代物,例如
磷酸酯、α-取代
磷酸酯和
磷硫酸酯的化合物。