Description
An S1P2 agonist (EC50 = 0.78 μM in a reporter assay); selective for S1P2 over S1P1 and S1P3-5 in a TGFα-shedding assay (EC50s = 119, 1,690, 1,950, >10,000, and >10,000 nM, respectively); reduces serum starvation-induced decreases in C6 rat glioma cell viability from 0.1-10 μM; reduces cisplatin-induced accumulation of ROS and apoptosis in C6 cells at 10 μM
Formal name: 1-[2-[2,5-dimethyl-1-(phenylmethyl)-1H-pyrrol-3-yl]-2-oxoethyl]-5-(trifluoromethyl)-2(1H)-pyridinone
Synonyms:
Molecular weight: 388.4
CAS: 870762-83-7
Purity: ≥98%
Formulation: A crystalline solid