| S7179 |
Siponimod (BAF312)
|
Siponimod (BAF312) is a next-generation S1P receptor agonist, selective for S1P1 and S1P5 receptors with EC50 of 0.39 nM and 0.98 nM, and it exhibits >1000-fold selectivity over S1P2, S1P3 and S1P4 receptors. This compound has reached Phase 3.
|
-
Cell Death Dis, 2025, 16(1):282
-
Cancers (Basel), 2024, 16(3)574
-
J Neuroinflammation, 2023, 20(1):35
|
|
| S6552 |
CYM5541
|
CYM5541 (ML249) is a selective, allosteric agonist of S1P3 with an EC50 of between 72 and 132 nM and exhibits exquisite selectivity over other S1P receptor subtypes in vitro: S1P1 EC50 > 10 μM, S1P2 EC50 > 50 μM, S1P4 EC50 > 50 μM, and S1P5 EC50 > 25 μM.
|
-
Brain Behav Immun, 2024, 124:205-217
|
|
| S4462 |
CYM-5520
|
CYM-5520 is a highly selective sphingosine-1-phosphate receptor 2 (S1PR2) agonist with an EC50 of 0.48 µM and does not activate other S1P receptors.
|
-
Front Pharmacol, 2024, 15:1494210
|
|
| S7180 |
SEW 2871
|
SEW2871 is an orally active, potent, and highly selective agonist of the sphingosine-1-phosphate type 1 receptor (S1P1) with an EC50 of 13.8 nM. It activates ERK, Akt, and Rac signalling pathways and induces S1P1 internalization and recycling.
|
-
Cell Death Dis, 2021, 12(11):1050
|
|
| E1999 |
Sphingosine-1-phosphate
|
Sphingosine-1-phosphate (S1P) is an agonist of S1P1-5 receptors and a ligand toGPR3, GPR6 and GPR12. It enhances GPR3-, GPR6-, and GPR12-mediated intracellular Ca²⁺ mobilization and regulates essential cellular processes such as proliferation, migration, cytoskeletal organization, adherens junction assembly, and morphogenesis.
|
|
|
| S3412 |
CYM50308
|
CYM50308 (ML248) is a potent and selective S1P4 receptor agonist with an EC50 of 56 nM.
|
|
|
| E4956 |
Ozanimod hydrochloride
|
Ozanimod hydrochloride(Zeposia, RPC-1063 HCL) is a potent sphingosine 1-phosphate (S1P)receptor modulator and a selective agonist of S1P receptor subtypes 1 (S1P1) and 5 (S1P5) with EC50's of 1.03 nM and 8.6 nM, respectively. It can be used in the trearment of relapsing multiple sclerosis (MS).
|
|
|