Sipatrigine
Author:
Publisher
Elsevier
Reference19 articles.
1. Phase II clinical trial of sipatrigine (619C89) by continuous infusion in acute stroke;Muir;Cerebrovasc. Dis.,2000
2. The neuroprotective agent sipatrigine (BW619C89) potently inhibits the human tandem pore-domain K+ channels TREK-1 and TRAAK;Meadows;Brain Res.,2001
3. Inhibition of human N-type voltage-gated Ca2+ channels by the neuroprotective agent BW619C89;McNaughton;Neuropharmacology,1997
4. Pharmacokinetics of 619C89, a novel neuronal sodium channel inhibitor, in acute stroke patients after loading and discrete maintenance infusions;Hussein;Br. J. Clin. Pharmacol.,1996
5. A comparison of the effects of a sodium channel blocker and an NMDA antagonist upon extracellular glutamate in rat focal cerebral ischemia;Chen;Brain Res.,1995
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