An update on sphingosine-1-phosphate receptor 1 modulators
- Bioorg Med Chem Lett. 2018 Dec 15;28(23-24):3585-3591. doi: 10.1016/j.bmcl.2018.10.042.
- 1. Department of Chemistry & Biochemistry, The University of Arizona, Tucson, AZ 85721, United States. Electronic address: [email protected].
- 2. Department of Medicine, The University of Arizona, Tucson, AZ 85724, United States. Electronic address: [email protected].
- 3. Department of Medicine, The University of Arizona, Tucson, AZ 85724, United States. Electronic address: [email protected].
- 4. Department of Chemistry & Biochemistry, The University of Arizona, Tucson, AZ 85721, United States. Electronic address: [email protected].
Sphingolipids represent an essential class of lipids found in all eukaryotes, and strongly influence cellular signal transduction. Autoimmune diseases like asthma and multiple sclerosis (MS) are mediated by the sphingosine-1-phosphate receptor 1 (S1P1) to express a variety of symptoms and disease patterns. Inspired by its natural substrate, an array of artificial sphingolipid derivatives has been developed to target this specific G protein-coupled receptor (GPCR) in an attempt to suppress autoimmune disorders. FTY720, also known as fingolimod, is the first oral disease-modifying therapy for MS on the market. In pursuit of improved stability, bioavailability, and efficiency, structural analogues of this initial prodrug have emerged over time. This review covers a brief introduction to the sphingolipid metabolism, the mechanism of action on S1P1, and an updated overview of synthetic sphingosine S1P1 agonists.