A new derivative of valproic acid amide possesses a broad-spectrum antiseizure profile and unique activity against status epilepticus and organophosphate neuronal damage

A new derivative of valproic acid amide possesses a broad-spectrum antiseizure profile and unique activity against status epilepticus and organophosphate neuronal damage

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http://www.wikidata.org/entity/Q35659046
α-Linolenic Acid, A Nutraceutical with Pleiotropic Properties That Targets Endogenous Neuroprotective Pathways to Protect against Organophosphate Nerve Agent-Induced NeuropathologyThe National Institute of Neurological Disorders and Stroke (NINDS) Epilepsy Therapy Screening Program (ETSP)Stereoselective anticonvulsant and pharmacokinetic analysis of valnoctamide, a CNS-active derivative of valproic acid with low teratogenic potential.The expression of kainate receptor subunits in hippocampal astrocytes after experimentally induced status epilepticus.Comments on the working group's 2012 review of the Program.Disease modification in epilepsy: from animal models to clinical applications.sec-Butylpropylacetamide (SPD) has antimigraine properties.Progress report on new antiepileptic drugs: A summary of the Thirteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XIII).Acute cognitive impact of antiseizure drugs in naive rodents and corneal-kindled mice.A rodent model of human organophosphate exposure producing status epilepticus and neuropathology.Mitochondrial Liver Toxicity of Valproic Acid and Its Acid Derivatives Is Related to Inhibition of α-Lipoamide Dehydrogenase.Valnoctamide and sec-butyl-propylacetamide (SPD) for acute seizures and status epilepticus.sec-Butylpropylacetamide (SPD), a new amide derivative of valproic acid for the treatment of neuropathic and inflammatory pain.A resurging boom in new drugs for epilepsy and brain disorders.sec-Butyl-propylacetamide (SPD) and two of its stereoisomers rapidly terminate paraoxon-induced status epilepticus in rats.Design and Comparative Evaluation of the Anticonvulsant Profile, Carbonic-Anhydrate Inhibition and Teratogenicity of Novel Carbamate Derivatives of Branched Aliphatic Carboxylic Acids with 4-Aminobenzensulfonamide.A companion to the preclinical common data elements for pharmacologic studies in animal models of seizures and epilepsy. A Report of the TASK3 Pharmacology Working Group of the ILAE/AES Joint Translational Task Force
P2860

A new derivative of valproic acid amide possesses a broad-spectrum antiseizure profile and unique activity against status epilepticus and organophosphate neuronal damage

Item
http://www.wikidata.org/entity/Q35659046
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2011 nî lūn-bûn
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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2011年论文
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2011年论文
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2011年论文
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name
A new derivative of valproic a ...... rganophosphate neuronal damage
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A new derivative of valproic a ...... rganophosphate neuronal damage
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A new derivative of valproic a ...... rganophosphate neuronal damage
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A new derivative of valproic a ...... rganophosphate neuronal damage
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A new derivative of valproic a ...... rganophosphate neuronal damage
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A new derivative of valproic a ...... rganophosphate neuronal damage
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10.1111/J.1528-1167.2011.03338.X
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