The present invention relates to new sphingolipid heterocyclic compounds as modulators of sphingolipid signaling and uses thereof as pharmaceutically active agents, suitable for treating proliferative, degenerative, infectious, and other diseases.
wherein X is selected from a methylene group (CH2) and oxygen (O);
and pharmaceutically acceptable salts thereof.
本发明涉及新的鞘脂异环化合物,作为鞘脂信号调节剂和药用活性剂的用途,适用于治疗增殖性、退行性、感染性和其他疾病。其中X选自亚甲基基(
CH2)和氧(O);以及其药学上可接受的盐。