Nafimidone hydrochloride

A highly potent agonist of NMDA and mGlu receptors. A frequently used brain-lesioning agent inducing excitotoxic lesions of neurons without damaging crossing fiber tracts.

Biochem/physiol Actions IC87201 is a potent inhibitor of the nNOS/PSD-95 protein-protein interaction that blocks NMDA-induced 3&#8242: ,5&#8242: -cyclic guanosine monophosphate (cGMP) production in hippocampal cultures. IC87201 exhibits analgesic

Lamotrigine is a novel anticonvulsant drug for inhibition of 5-HT with IC50 of 240 μM and 474 μM in human platelets and rat brain synaptosomes, and also is a sodium channel blocker.A sodium channel protein inhibitor.

Lamotrigine is a novel anticonvulsant drug for inhibition of 5-HT with IC50 of 240 μM and 474 μM in human platelets and rat brain synaptosomes, and also is a sodium channel blocker.A sodium channel protein inhibitor.

Lamotrigine is a novel anticonvulsant drug for inhibition of 5-HT with IC50 of 240 μM and 474 μM in human platelets and rat brain synaptosomes, and also is a sodium channel blocker.A sodium channel protein inhibitor.

Lamotrigine is a novel anticonvulsant drug for inhibition of 5-HT with IC50 of 240 μM and 474 μM in human platelets and rat brain synaptosomes, and also is a sodium channel blocker.A sodium channel protein inhibitor.

LIT-001 is the first nonpeptide oxytocin receptor (OT-R) agonist ( EC 50 =55 nM: K i =226 nM). LIT-001 improves social interaction in a mouse model of autismIn VitroIn vitro signaling experiments, LIT-001 is a nonbiased OT-R agonist on the two main

LIT-001 is the first nonpeptide oxytocin receptor (OT-R) agonist ( EC 50 =55 nM: K i =226 nM). LIT-001 improves social interaction in a mouse model of autismIn VitroIn vitro signaling experiments, LIT-001 is a nonbiased OT-R agonist on the two main

LIT-001 is the first nonpeptide oxytocin receptor (OT-R) agonist ( EC 50 =55 nM: K i =226 nM). LIT-001 improves social interaction in a mouse model of autismIn VitroIn vitro signaling experiments, LIT-001 is a nonbiased OT-R agonist on the two main

Immunogen Fusion protein amino acids 1-215 (full-length) of rat NavBeta3 Physical form PBS pH 7.4, 50% glyercol, 0.

N-Acetyl lysyltyrosylcysteine amide is a potent, reversible, specific, and non-toxic tripeptide inhibitor of myeloperoxidase (MPO). N-Acetyl lysyltyrosylcysteine amide effectively inhibits MPO generation of toxic oxidants in vivo. N-Acetyl

N-Acetyl lysyltyrosylcysteine amide is a potent, reversible, specific, and non-toxic tripeptide inhibitor of myeloperoxidase (MPO). N-Acetyl lysyltyrosylcysteine amide effectively inhibits MPO generation of toxic oxidants in vivo. N-Acetyl