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首页> 外文期刊>Future medicinal chemistry >Discovery of fingolimod, the sphingosine 1-phosphate receptor modulator and its application for the therapy of multiple sclerosis
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Discovery of fingolimod, the sphingosine 1-phosphate receptor modulator and its application for the therapy of multiple sclerosis

机译:芬戈莫德,1-磷酸鞘氨醇受体调节剂的发现及其在多发性硬化症治疗中的应用

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Fingolimod (FTY720) is a first-in-class, orally active, sphingosine 1-phosphate (S1P)-receptor modulator with a structure closely related to sphingosine. The compound was discovered by chemical modification of a natural product, myriocin. Phosphorylated form of FTY720 acts as a functional antagonist at S1P receptor type 1 (S1P 1), inhibits lymphocyte egress from secondary lymphoid organs and shows immunomodulating effects. Phase III studies in multiple sclerosis demonstrated that oral FTY720 had superior efficacy compared with intramuscular IFN-β1a (AVONEX ?) with regard to reducing the rate of relapse and the number of inflammatory lesions in the CNS. FTY720 has been approved as a new therapeutic drug for multiple sclerosis in more than 50 countries, including the USA, Japan and some of those in the EU.
机译:芬戈莫德(FTY720)是一流的口服活性鞘氨醇1-磷酸(S1P)受体调节剂,其结构与鞘氨醇密切相关。该化合物是通过对天然产物myriocin进行化学修饰而发现的。 FTY720的磷酸化形式可作为1型S1P受体(S1P 1)的功能性拮抗剂,抑制淋巴细胞从次级淋巴器官流出,并显示免疫调节作用。在多发性硬化症中进行的III期研究表明,在降低中枢神经系统的复发率和炎性病变数量方面,口服FTY720优于肌内IFN-β1a(AVONEX®)。 FTY720已在50多个国家(包括美国,日本和某些欧盟国家)被批准为多发性硬化症的新治疗药物。

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