What is he best known for?
The fields of study he is best known for:
- Organic chemistry
- Anticonvulsant
- Biochemistry
James P. Stables mostly deals with Anticonvulsant, Stereochemistry, Chemical synthesis, Pharmacology and Epilepsy.
His Anticonvulsant research integrates issues from Oral administration, ED50, Structure–activity relationship, Phenytoin and Carboxamide.
His Stereochemistry study integrates concerns from other disciplines, such as Aryl, Isatin and Mechanism of action.
The various areas that he examines in his Chemical synthesis study include Hydrazone, Hydrogen bond, Pharmacophore, Biological activity and Semicarbazone.
His Pharmacology research incorporates elements of Neurotoxicity and Hydrazide.
James P. Stables combines subjects such as Central nervous system disease and Intensive care medicine with his study of Epilepsy.
His most cited work include:
- Anticonvulsant activity of Schiff bases of isatin derivatives. (247 citations)
- Anticonvulsant activity of hydrazones, Schiff and Mannich bases of isatin derivatives. (203 citations)
- Anticonvulsant properties of various acetylhydrazones, oxamoylhydrazones and semicarbazones derived from aromatic and unsaturated carbonyl compounds. (196 citations)
What are the main themes of his work throughout his whole career to date?
James P. Stables focuses on Anticonvulsant, Stereochemistry, Pharmacology, Chemical synthesis and Neurotoxicity.
His Anticonvulsant research is multidisciplinary, relying on both Oral administration, Semicarbazone, Phenytoin and Strychnine.
The Stereochemistry study combines topics in areas such as Aryl and Structure–activity relationship.
His Structure–activity relationship research focuses on Cytotoxicity and how it relates to Enone.
His Pharmacology research is multidisciplinary, incorporating perspectives in Receptor, Pentylenetetrazol, Sodium channel and Epilepsy.
As a member of one scientific family, James P. Stables mostly works in the field of Chemical synthesis, focusing on Amino acid and, on occasion, Seizure threshold.
He most often published in these fields:
- Anticonvulsant (69.33%)
- Stereochemistry (52.00%)
- Pharmacology (34.00%)
What were the highlights of his more recent work (between 2009-2013)?
- Anticonvulsant (69.33%)
- Stereochemistry (52.00%)
- Pharmacology (34.00%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Anticonvulsant, Stereochemistry, Pharmacology, Structure–activity relationship and Neurotoxicity.
James P. Stables has included themes like Antiepileptic drug and ED50 in his Anticonvulsant study.
His work on Pharmacophore as part of his general Stereochemistry study is frequently connected to Active compound, thereby bridging the divide between different branches of science.
His biological study spans a wide range of topics, including Receptor, Local anesthetic, Antioxidant and Sodium channel.
His studies deal with areas such as Pyridine, Active metabolite, Imidazole, Lacosamide and Stereoisomerism as well as Structure–activity relationship.
His Neurotoxicity study incorporates themes from Oral administration, Nafimidone, Antimicrobial, Prodrug and Carbamazepine.
Between 2009 and 2013, his most popular works were:
- Identification of new epilepsy treatments: Issues in preclinical methodology (168 citations)
- A New Derivative of Valproic Acid Amide Possesses a Broad-spectrum Antiseizure Profile and Unique Activity Against Status Epilepticus and Organophosphate Neuronal Damage (55 citations)
- Synthesis, anticonvulsant and antimicrobial activities of some new 2-acetylnaphthalene derivatives. (52 citations)
In his most recent research, the most cited papers focused on:
- Organic chemistry
- Biochemistry
- Internal medicine
His primary areas of study are Anticonvulsant, Stereochemistry, Structure–activity relationship, Lacosamide and Pharmacophore.
The concepts of his Anticonvulsant study are interwoven with issues in Prodrug, Pharmacology and Valproic Acid.
James P. Stables interconnects Nafimidone, Aryl, Antimicrobial and Active metabolite in the investigation of issues within Stereochemistry.
His Structure–activity relationship study combines topics from a wide range of disciplines, such as Neurotoxicity, Maximal electroshock, Stereoisomerism, Rats sprague dawley and Phenytoin.
His Lacosamide study combines topics from a wide range of disciplines, such as Adjuvant, Central nervous system, Neuron and Sodium channel.
His research investigates the connection between Pharmacophore and topics such as Design synthesis that intersect with problems in Binding properties, Hydrogen bond and Pyridine.
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