Perzinfotel displays high affinity (IC50=30 nM) for the glutamate site. Perzinfotel is an effective, selective, and competitive NMDA receptor antagonist with neuroprotective effects.

Perzinfotel blocks NMDA-induced currents (IC50: 0.48 μM) and glutamate-induced neurotoxicity (IC50: 1.6 μM)[1].

144912-63-0

C9H13N2O5P

260.18

EAA-090

(< 1 mg/ml refers to the product slightly soluble or insoluble )
Powder: -20°C for 3 years
In solvent: -80°C for 2 years