Pharmacokinetic Analysis and Antiepileptic Activity of Tetra-Methylcyclopropane Analogues of Valpromide
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Summary
The antiepileptic potential of tetramethylcyclopropane analogues of VPD are discussed which are in animal models more potent than VPA and may be non-teratogenic and non-hepatotoxic.
- Type
- article
- Published
- 1996-02-01
- Cited by
- 22
- References
- 17
- OpenAlex
- https://openalex.org/W308130168
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:3162468
Keywords
Pharmacokinetics, Tetra, Chemistry, Pharmacology, Anticonvulsant
References
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- Pharmacokinetic Analysis of the Structural Requirements for Forming “Stable” Analogues of Valpromide
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- Can we develop improved derivatives of valproic acid?
- Sodium Valproate in the Induction of Unusual Hepatotoxicity
- 1-aminocyclopropanecarboxylates exhibit antidepressant and anxiolytic actions in animal models.
- Rapid gas chromatographic assay for monitoring valnoctamide in plasma.
- Noncompartmental determination of the steady-state volume of distribution.
- Valproate‐Induced Hepatic Injury: Analyses of 23 Fatal Cases
- Clinical Pharmacology of Valpromide
- Valproic acid-induced neural tube defects in mouse and human: aspects of chirality, alternative drug development, pharmacokinetics and possible mechanisms.
- Statistical moments in pharmacokinetics
- Structure-pharmacokinetic relationships in a series of short fatty acid amides that possess anticonvulsant activity.
- 1-Aminocyclopropane-1-carboxylic acid (ACC) mimics the effects of glycine on the NMDA receptor ion channel.
- Antiepileptic Drug Development Program.
- Valproic acid teratogenesis
Cited by
- Theoretical characterization of SOME amides and esters DERIVATIVES of valproic acid
- Comparative pharmacodynamic and pharmacokinetic analysis of two anticonvulsant halo derivatives of 2,2,3,3‐tetramethylcyclopropanecarboxamide, an amide of a cyclic analog of valproic acid
- Structure Activity Relationship of Human Microsomal Epoxide Hydrolase Inhibition by Amide and Acid Analogues of Valproic Acid
- Pharmacokinetics and Antiepileptic Activity of Valproyl Hydroxamic Acid Derivatives
- Efficacy of antiepileptic tetramethylcyclopropyl analogues of valproic acid amides in a rat model of neuropathic pain.
- Propylisopropylacetic acid (PIA), a constitutional isomer of valproic acid, uncompetitively inhibits arachidonic acid acylation by rat acyl-CoA synthetase 4: a potential drug for bipolar disorder
- Characterization of the anticonvulsant profile of valpromide derivatives.
- Valproic acid: Second generation
- Anticonvulsant efficacy of valproate-like carboxylic acids: a potential target for anti-bipolar therapy.
- Anticonvulsant Profile and Teratogenicity of N‐methyl‐tetramethylcyclopropyl Carboxamide: A New Antiepileptic Drug
- New CNS-active drugs which are second-generation valproic acid: can they lead to the development of a magic bullet?
- The Effects of Central Nervous System-Active Valproic Acid Constitutional Isomers, Cyclopropyl Analogs, and Amide Derivatives on Neuronal Growth Cone Behavior
- Valproate decreases inositol biosynthesis.
- Metabolism of a new antiepileptic drug, N-methyl-tetramethylcyclopropanecarboxamide, and anticonvulsant activity of its metabolites.
- New CNS-active drugs which are second-generation valproic acid
- Pulmonary and general pharmacokinetic studies on racemic ethosuximide using a chiral sensitive GC/MS technique.
- Developing an in vitro model of haemorrhagic shock to investigate the molecular mechanism of valproic acid in the treatment of massive blood loss
- Insights into Structural Modifications of Valproic Acid and Their Pharmacological Profile
- Valproic acid as a therapeutic scaffold: Advances in structural modification and drug design.
- SYNTHESIS AND ANTICONVULSANT STUDIES OF ISOMERIC N-BENZYL-3- ((METHYLPHENYL) AMINO) PROPANAMIDES
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