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Multiple Sclerosis

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Cat. No. Product Name Field of Application Chemical Structure
DC7675 BX-471(ZK 811752) Featured BX471 is a potent, selective non-peptide CCR1 antagonist (Ki = 1 nM for human CCR1); exhibits 250-fold selectivity for CCR1 over CCR2, CCR5 and CXCR4.
DC10357 Cenerimod Cenerimod (ACT-334441) is a potent and orally available sphingosine 1-phosphate 1 receptor (S1P1) agonist extracted from patent WO 2016184939 A1 and WO 2011007324 A1, example 1, with an EC50 of 2.7 nM.
DC8936 Fingolimod Fingolimod(FTY720 free base) is a S1P antagonist with IC50 of 0.033 nM.
DC3154 Fingolimod HCl(FTY-720) Featured FTY720 (Fingolimod, Gilenya) is a S1P antagonist with IC50 of 0.033 nM.
DC2071 ABR-215062 (Laquinimod) Featured Laquinimod (ABR-215062) is a potent immunomodulator.
DC3167 MK0812 MK-0812 is chemokine receptor CCR-2 antagonist
DC8281 Ozanimod (RPC1063) Featured Ozanimod (RPC1063) is a selective S1P1R modulator
DC8741 Plerixafor octahydrochloride Featured Plerixafor octahydrochloride(AMD3100 8HCL) is a chemokine receptor antagonist for CXCR4 and CXCL12-mediated chemotaxis with IC50 of 44 nM and 5.7 nM, respectively.
DC9742 Ponesimod Featured Ponesimod(ACT-128800) is an orally active, selective sphingosine-1-phosphate receptor 1 (S1P1) immunomodulator with EC50 of 5.7 nM.
DC9490 Zaurategrast Zaurategrast(CDP-323) is an oral α4-integrin inhibitor.
DC12355 Ceralifimod (ONO-4641) Ceralifimod is selective, high potent agonist for sphingosine 1-phosphate receptors 1 and 5, with EC50s of 27.3, 334 pM for human S1P receptor 1 and 5, respectively.
DC7694 BAF312 (Siponimod) Featured BAF312 is a potent and selective agonist of S1P with EC50 value of 0.39nM for S1P1 receptors and 0.98nM for S1P5 receptors, respectively
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