| S5002 |
FTY720 (Fingolimod) Hydrochloride
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Fingolimod (FTY720, Fingolimod Hydrochloride) HCl is a S1P antagonist with IC50 of 0.033 nM in K562, and NK cells. Please use saline solution rather than PBS for dilutions. PBS may cause precipitation.
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Cancer Cell, 2025, S1535-6108(25)00319-8
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Nat Commun, 2025, 16(1):9175
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Nat Commun, 2025, 16(1):1826
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| S7182 |
JTE 013
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JTE 013 is a potent and selective S1P2 antagonist with IC50 of 17.6 nM.
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Cell Death Dis, 2025, 16(1):282
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Front Pharmacol, 2024, 15:1494210
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Cell Res, 2022, 10.1038/s41422-022-00614-0
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| E1158 |
CAY10444
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CAY10444 (BML-241) is a sphingosine-1-phosphate 3 (S1P3) antagonist, which can inhibit S1P response of S1P3 cell line with 78% inhibition rate and IC50 of 4.6 μM.
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Cell Death Dis, 2025, 16(1):282
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J Transl Med, 2025, 23(1):573
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| E2363 |
Etrasimod(APD334)
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Etrasimod(APD334) is a potent, selective and orally available antagonist of the sphingosine-1-phosphate-1 (S1P1) receptor with an EC50 value of 1.88 nM in CHO cells.
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| S7181 |
W146
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W146 is a selective antagonist of sphingosine-1-phosphate receptor 1 (S1PR1) with an EC50 value of 398 nM. It may exhibit potential clinical applications in multiple sclerosis, coronary artery disease, diabetes, and cancer treatment.
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