The methylene and sulfur analogues of sphingosine 1-phosphate labeled with a fluorescent group at the terminus of the backbone skeleton were stereoselectively synthesized as possible nonhydrolyzable visible ligands to the sphingosine 1-phosphate receptor, S1P1.
我们立体选择性地合成了在骨架骨架末端标有荧光基团的 1-
磷酸鞘氨醇亚甲基和
硫类似物,它们可能是 1-
磷酸鞘氨醇受体 S1P1 的非
水解可见
配体。