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progabide

Known as: Butanamide, 4-(((4-chlorophenyl)(5-fluoro-2-hydroxyphenyl)methylene)amino)-, Progabida, Progabidum 
National Institutes of Health

Related topics

Related topics

8 relations

Broader (5)

AnticonvulsantsAntidepressive AgentsAntiparkinson AgentsGABA Agonists

Narrower (2)

GabreneSL 76002
analogs & derivatives

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
1999
Review
1999
The treatment of tardive dyskinesia—a systematic review and meta-analysis
Highly Cited
1997
Highly Cited
1997
Mechanisms of the inhibition of human erythrocyte pyridoxal kinase by drugs.
Review
1997
Review
1997
Traditional pharmacological treatments for spasticity part II: General and regional treatments
Systemic pharmacologic treatments may be indicated in conditions in which the distribution of muscle overactivity is diffuse… 
1990
1990
Are GABAB receptors involved in the pharmacological effects of ethanol?
Highly Cited
1986
Highly Cited
1986
Anticonvulsant profile of drugs which facilitate gabaergic transmission on convulsions mediated by a gabaergic mechanism
Highly Cited
1985
Highly Cited
1985
Antagonism of N-methyl-D,L-aspartic acid-induced convulsions by antiepileptic drugs and other agents.
Highly Cited
1982
Highly Cited
1982
Comparative assay of anticonvulsant and toxic potencies of sixteen GABAmimetic drugs
Highly Cited
1982
Highly Cited
1982
gamma-Aminobutyric acid (GABA) receptor stimulation. II. Specificity of progabide (SL 76002) and SL 75102 for the GABA receptor.
Progabide and its immediate metabolite SL 75102 displace [3H]gamma-aminobutyric acid (GABA), [3H]muscimol and [3H]isoguvacine… 
Highly Cited
1982
Highly Cited
1982
gamma-Aminobutyric acid (GABA) receptor stimulation. I. Neuropharmacological profiles of progabide (SL 76002) and SL 75102, with emphasis on their anticonvulsant spectra.
Progabide (4-([(4-chlorophenyl) (5-fluoro-2-hydroxyphenyl)-methylene]amino) butanamide) is a gamma-aminobutyric acid (GABA… 
Highly Cited
1982
Highly Cited
1982
Enhancing GABAergic transmission reverses the aversive state in rats induced by electrical stimulation of the periaqueductal grey region
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