About 3 results found for searched term "Fingolimod" (0.357 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M1712 | FTY720 hydrochloride | S1P Receptor |
| Fingolimod hydrochloride | ||
| Fingolimod (FTY720) HCl is a 1-phospho-neuraminol S1P receptor antagonist with an IC50 of 0.33 nM. , FTY720 can dephosphorylate AMPK by activating PP2A and reduce the expression level of phosphorylated eEF2K, ultimately leading to ADCD and iron death in human multiple myeloma cells. | ||
| M14000 | Fingolimod | S1P Receptor |
| FTY720 free base | ||
| Fingolimod (FTY720 free base) is a sphingosine 1-phosphate (S1P) antagonist with an IC50 of 0.033 nM in K562 and NK cells. Fingolimod also is a pak1 activator, a immunosuppressant. | ||
| M7570 | Amiselimod hydrochloride | S1P Receptor |
| MT-1303 hydrochloride | ||
| Amiselimod hydrochloride is a novel sphingosine 1-phosphate receptor-1 (S1P1) modulator, designed to reduce the bradycardia effects associated with fingolimod and other S1P receptor modulators. | ||
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