10-hydroxycarbamazepine has been researched along with eslicarbazepine in 5 studies
| Studies (10-hydroxycarbamazepine) | Trials (10-hydroxycarbamazepine) | Recent Studies (post-2010) (10-hydroxycarbamazepine) | Studies (eslicarbazepine) | Trials (eslicarbazepine) | Recent Studies (post-2010) (eslicarbazepine) |
|---|---|---|---|---|---|
| 106 | 20 | 30 | 42 | 3 | 40 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (60.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alves, PC; Benes, J; Cunha, RA; Figueiredo, AA; Freitas, AP; Garrett, J; Learmonth, DA; Parada, A; Soares-da-Silva, P | 1 |
| Czendlik, C; Flesch, G; Lloyd, P; Renard, D | 1 |
| Almeida, A; Alves, G; Falcão, A; Fortuna, A; Lopes, B; Soares-da-Silva, P | 1 |
| Crommen, J; Fillet, M; Janicot, B; Servais, AC; Takam, A | 1 |
| Bayraktar, E; Eltokhi, A; Hedrich, UBS; Lauxmann, S; Lerche, H; Liu, Y; Lyu, H; Sara, Y; Sonnenberg, L; Wuttke, TV | 1 |
1 trial(s) available for 10-hydroxycarbamazepine and eslicarbazepine
| Article | Year |
|---|---|
Pharmacokinetics of the monohydroxy derivative of oxcarbazepine and its enantiomers after a single intravenous dose given as racemate compared with a single oral dose of oxcarbazepine.
Topics: Administration, Oral; Adult; Anticonvulsants; Biological Availability; Carbamazepine; Cross-Over Studies; Dose-Response Relationship, Drug; Female; Humans; Infusions, Intravenous; Male; Metabolic Clearance Rate; Molecular Structure; Reproducibility of Results; Stereoisomerism; Tissue Distribution | 2011 |
4 other study(ies) available for 10-hydroxycarbamazepine and eslicarbazepine
| Article | Year |
|---|---|
Anticonvulsant and sodium channel-blocking properties of novel 10,11-dihydro-5H-dibenz[b,f]azepine-5-carboxamide derivatives.
Topics: Amides; Animals; Anticonvulsants; Azepines; Calcium Channel Blockers; Calcium Channels; Cerebral Cortex; Electroshock; In Vitro Techniques; Ion Channel Gating; Motor Activity; Prodrugs; Rats; Seizures; Sodium; Stereoisomerism; Structure-Activity Relationship; Synaptosomes | 1999 |
A chiral liquid chromatography method for the simultaneous determination of oxcarbazepine, eslicarbazepine, R-licarbazepine and other new chemical derivatives BIA 2-024, BIA 2-059 and BIA 2-265, in mouse plasma and brain.
Topics: Animals; Anticonvulsants; Brain; Calibration; Carbamazepine; Chromatography, Liquid; Dibenzazepines; Mice; Oxcarbazepine; Quality Control; Reference Standards; Spectrophotometry, Ultraviolet; Stereoisomerism | 2012 |
Liquid chromatography separation of the chiral prodrug eslicarbazepine acetate and its main metabolites in polar organic mode. Application to their analysis after in vitro metabolism.
Topics: Acetic Acid; Acetonitriles; Carbamazepine; Cellulose; Chromatography, Liquid; Dibenzazepines; Diethylamines; Humans; Microsomes, Liver; Oxcarbazepine; Phenylcarbamates; Prodrugs; Solid Phase Extraction; Solvents; Stereoisomerism | 2016 |
In vitro effects of eslicarbazepine (S-licarbazepine) as a potential precision therapy on SCN8A variants causing neuropsychiatric disorders.
Topics: Animals; Dibenzazepines; Epilepsy; Mice; Mutation; NAV1.6 Voltage-Gated Sodium Channel | 2023 |