S1P receptor
S1P (sphinogosine-1-phosphate) receptor is a G-protein coupled receptor that involved in regulation of cells proliferation, survival, motility and adhesion etc.
Products Related to S1P receptor(8)
- GC14807Fingolimod (FTY720) HClCAS: 162359-56-0Purity: >99.00%
Fingolimod (FTY720), an immunosuppressant agent, usually used in the treatment of multiple sclerosis, also has anticancer actions and can act as an HDACi (Histone deacetylase inhibitors)[1].
- GC14360Ozanimod (RPC1063)CAS: 1306760-87-1Purity: >99.50%
Ozanimod (RPC1063) is a sphingosine-1-phosphate (S1P) receptor modulator that can cross the blood-brain barrier. Ozanimod selectively binds to S1P1 (EC 50 =1.03nM) and S1P5 (EC 50 =8.6nM) receptors.
- GC17201BAF312 (Siponimod)CAS: 1230487-00-9Purity: >99.00%
BAF312 (Siponimod) is a selective and orally active sphingosine-1-phosphate (S1P) receptor agonist, with the EC 50 values of 0.39, 750, and 0.98nM for S1P1, S1P4, and S1P5 receptors, respectively.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC14807 | Fingolimod (FTY720) HCl | 162359-56-0 | >99.00% | |
Fingolimod (FTY720), an immunosuppressant agent, usually used in the treatment of multiple sclerosis, also has anticancer actions and can act as an HDACi (Histone deacetylase inhibitors)[1]. | ||||
| GC16701 | SKI II | 312636-16-1 | >98.00% | |
Sphingosine kinase(SK) inhibitor | ||||
| GC11917 | PF-543 | 1415562-82-1 | >98.00% | |
PF-543 is a potent, selective, reversible, and sphingosine-competitive inhibitor of SphK1 with an IC 50 value of 2nM and a Ki value of 3.6 nM. | ||||
| GC14360 | Ozanimod (RPC1063) | 1306760-87-1 | >99.50% | |
Ozanimod (RPC1063) is a sphingosine-1-phosphate (S1P) receptor modulator that can cross the blood-brain barrier. Ozanimod selectively binds to S1P1 (EC 50 =1.03nM) and S1P5 (EC 50 =8.6nM) receptors. | ||||
| GC16660 | Ponesimod | 854107-55-4 | >98.00% | |
sphingosine-1-phosphate receptor 1 (S1P1) modulator | ||||
| GC42664 | A-971432 | 1240308-45-5 | >98.00% | |
A-971432 is a sphingosine-1-phosphate receptor 5 (S1P5) agonist that is selective for S1P5 over S1P1 and S1P3 (IC50s = 0.006, 0.362, and >10 μM, respectively). | ||||
| GC50275 | Ex 26 | 1233332-37-0 | >98% | |
Potent and selective S1P1 receptor antagonist | ||||
| GC17201 | BAF312 (Siponimod) | 1230487-00-9 | >99.00% | |
BAF312 (Siponimod) is a selective and orally active sphingosine-1-phosphate (S1P) receptor agonist, with the EC 50 values of 0.39, 750, and 0.98nM for S1P1, S1P4, and S1P5 receptors, respectively. | ||||
