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Use-Dependent Inhibition of the N-Methyl-D-aspartate Currents by Felbamate: a Gating Modifier with Selective Binding to the Desensitized Channels
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ana.410350216openalex-snapshot
Mechanism of action of the anticonvulsant felbamate: Opposing effects on N ‐methyl‐ D ‐aspartate and γ‐aminobutyric acid A receptors
inferredcites →https://doi.org/10.1002/ana.410360423openalex-snapshot
Mechanism of action of the anticonvulsant felbamate: Opposing effects on N‐methyl‐ D ‐aspartate and γ‐aminobutyric acid A receptors
inferredcites →https://doi.org/10.1016/0006-8993(95)01147-1openalex-snapshot
Excitoprotective effect of felbamate in cultured cortical neurons
inferredcites →https://doi.org/10.1016/0896-6273(94)90335-2openalex-snapshot
Na+ channels must deactivate to recover from inactivation
inferredcites →https://doi.org/10.1016/s0006-3495(96)79724-2openalex-snapshot
Three-dimensional models of non-NMDA glutamate receptors
inferredcites →https://doi.org/10.1016/s0014-2999(96)00802-3openalex-snapshot
Felbamate inhibits cloned voltage-dependent Na+ channels from human and rat brain
inferredcites →https://doi.org/10.1016/s0022-3565(24)36535-8openalex-snapshot
Barbiturate-Like Actions of the Propanediol Dicarbamates Felbamate and Meprobamate
inferredcites →https://doi.org/10.1016/s0022-3565(24)37679-7openalex-snapshot
Felbamate Increases [3H]Glycine Binding in Rat Brain and Sections of Human Postmortem Brain
inferredcites →https://doi.org/10.1016/s0022-3565(24)38215-1openalex-snapshot
Subtype-Selective Antagonism of N-Methyl-d-Aspartate Receptors by Felbamate: Insights into the Mechanism of Action
inferredcites →https://doi.org/10.1016/s0022-3565(25)09605-3openalex-snapshot
Felbamate block of the N-methyl-D-aspartate receptor.
inferredcites →https://doi.org/10.1016/s0022-3565(25)10138-9openalex-snapshot
Evidence for anticonvulsant and neuroprotectant action of felbamate mediated by strychnine-insensitive glycine receptors.
inferredcites →https://doi.org/10.1016/s0022-3565(25)12797-3openalex-snapshot
Felbamate inhibits dihydropyridine-sensitive calcium channels in central neurons.
inferredcites →https://doi.org/10.1016/s0022-3565(25)21266-6openalex-snapshot
Felbamate decreases synaptic transmission in the CA1 region of rat hippocampal slices.
inferredcites →https://doi.org/10.1016/s0026-895x(24)13073-8openalex-snapshot
A Common Anticonvulsant Binding Site for Phenytoin, Carbamazepine, and Lamotrigine in Neuronal Na+ Channels
inferredcites →https://doi.org/10.1016/s0026-895x(25)09749-4openalex-snapshot
Excitatory amino acid receptors expressed in Xenopus oocytes: agonist pharmacology.
inferredcites →https://doi.org/10.1016/s0026-895x(25)09804-9openalex-snapshot
Slow binding of phenytoin to inactivated sodium channels in rat hippocampal neurons.
inferredcites →https://doi.org/10.1016/s0090-9556(25)08294-7openalex-snapshot
Drug concentrations in human brain tissue samples from epileptic patients treated with felbamate.
inferredcites →https://doi.org/10.1016/s0896-6273(00)80228-7openalex-snapshot
Identification of the Amino Acid Subsets Accounting for the Ligand Binding Specificity of a Glutamate Receptor
inferredcites →https://doi.org/10.1016/s0896-6273(00)80459-6openalex-snapshot
N-Terminal Domains in the NR2 Subunit Control Desensitization of NMDA Receptors
inferredcites →https://doi.org/10.1016/s0896-6273(00)80972-1openalex-snapshot
Identification of Amino Acid Residues that Control Functional Behavior in GluR5 and GluR6 Kainate Receptors
inferredcites →https://doi.org/10.1038/27692openalex-snapshot
Structure of a glutamate-receptor ligand-binding core in complex with kainate
inferredcites →https://doi.org/10.1038/325529a0openalex-snapshot
Glycine potentiates the NMDA response in cultured mouse brain neurons
inferredcites →https://doi.org/10.1038/3661openalex-snapshot
Phenylethanolamines inhibit NMDA receptors by enhancing proton inhibition
inferredcites →https://doi.org/10.1038/sj.bjp.0701221openalex-snapshot
Characterization of lamotrigine inhibition of Na+ channels in rat hippocampal neurones
inferredcites →https://doi.org/10.1042/bst0260450openalex-snapshot
Three-dimensional models of glutamate receptors
inferredcites →https://doi.org/10.1056/nejm199301073280105openalex-snapshot
Efficacy of Felbamate in Childhood Epileptic Encephalopathy (Lennox-Gastaut Syndrome)
inferredcites →https://doi.org/10.1073/pnas.87.6.2354openalex-snapshot
Glycine decreases desensitization of N-methyl-D-aspartate (NMDA) receptors expressed in Xenopus oocytes and is required for NMDA responses.
inferredcites →https://doi.org/10.1073/pnas.92.22.10327openalex-snapshot
Desensitization of N-methyl-D-aspartate receptors: a problem of interpretation.
inferredcites →https://doi.org/10.1074/jbc.271.16.9603openalex-snapshot
Interactions between Ifenprodil and the NR2B Subunit of the N-Methyl-D-aspartate Receptor
inferredcites →https://doi.org/10.1111/j.1528-1157.1986.tb03497.xopenalex-snapshot
Comparative Anticonvulsant Activity and Neurotoxicity of Felbamate and Four Prototype Antiepileptic Drugs in Mice and Rats
inferredcites →https://doi.org/10.1111/j.1528-1157.1991.tb04668.xopenalex-snapshot
Felbamate: A Clinical Trial for Complex Partial Seizures
inferredcites →https://doi.org/10.1111/j.1528-1157.1997.tb00061.xopenalex-snapshot
Felbamate: 1997 Update
inferredcites →https://doi.org/10.1111/j.1528-1157.1997.tb00062.xopenalex-snapshot
Evaluation of Case Reports of Aplastic Anemia Among Patients Treated with Felbamate
inferredcites →https://doi.org/10.1113/jphysiol.1992.sp019148openalex-snapshot
Activation and desensitization of N‐methyl‐D‐aspartate receptors in nucleated outside‐out patches from mouse neurones.
inferredcites →https://doi.org/10.1113/jphysiol.1996.sp021807openalex-snapshot
A novel mechanism of activity‐dependent NMDA receptor antagonism describes the effect of ifenprodil in rat cultured cortical neurones.
inferredcites →https://doi.org/10.1124/mol.51.6.1077openalex-snapshot
Carbamazepine Inhibition of Neuronal Na+ Currents: Quantitative Distinction from Phenytoin and Possible Therapeutic Implications
inferredcites →https://doi.org/10.1126/science.2841759openalex-snapshot
Requirement for Glycine in Activation of NMDA-Receptors Expressed in Xenopus Oocytes
inferredcites →https://doi.org/10.1212/wnl.41.11.1785openalex-snapshot
Felbamate for partial seizures
inferredcites →https://doi.org/10.1523/jneurosci.10-07-02385.1990openalex-snapshot
Structure-activity relationships for amino acid transmitter candidates acting at N-methyl-D-aspartate and quisqualate receptors
inferredcites →https://doi.org/10.1523/jneurosci.14-04-02153.1994openalex-snapshot
Both open and closed NMDA receptor channels desensitize
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1007/s40265-018-0959-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.eplepsyres.2007.09.005openalex-snapshot
Felbamate but not phenytoin or gabapentin reduces glutamate release by blocking presynaptic NMDA receptors in the entorhinal cortex
inferred← citeshttps://doi.org/10.1016/j.nbd.2020.105188openalex-snapshot
Glutamate transmission rather than cellular pacemaking propels excitatory-inhibitory resonance for ictogenesis in amygdala
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Astroglial d-serine is the endogenous co-agonist at the presynaptic NMDA receptor in rat entorhinal cortex
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Molecular Targets for Antiepileptic Drug Development
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Molecular Nanoinformatics Approach Assessing the Coating Oxcarbazepine (OXC) Drug on Silver Nanoparticles
inferred← citeshttps://doi.org/10.1021/jm0706618openalex-snapshot
Molecular Determinants of the Anticonvulsant Felbamate Binding Site in theN-Methyl- d -Aspartate Receptor
inferred← citeshttps://doi.org/10.1038/nrn1430openalex-snapshot
The neurobiology of antiepileptic drugs
inferred← citeshttps://doi.org/10.1038/srep37029openalex-snapshot
Modulation of NMDA channel gating by Ca2+ and Cd2+ binding to the external pore mouth
inferred← citeshttps://doi.org/10.1053/j.ajkd.2018.03.021openalex-snapshot
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inferred← citeshttps://doi.org/10.1093/brain/awh682openalex-snapshot
Molecular and cellular mechanisms of pharmacoresistance in epilepsy.
inferred← citeshttps://doi.org/10.1093/med/9780199746545.003.0083openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/jnc.14939openalex-snapshot
Desensitization of NMDA channels requires ligand binding to both GluN1 and GluN2 subunits to constrict the pore beside the activation gate
inferred← citeshttps://doi.org/10.1113/jphysiol.2009.178913openalex-snapshot
Ionic flow enhances low-affinity binding: a revised mechanistic view into Mg2+block of NMDA receptors
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NMDA receptor binding in focal epilepsies
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Modifications of Antiepileptic Drugs for Improved Tolerability and Efficacy
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Allosteric Interactions at the NMDA Receptor Channel Complex
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Neuroprotective Strategies Using Antiepileptic Drugs
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Mechanisms of Antiepileptic Drug Action
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The Activation Gate and Gating Mechanism of the NMDA Receptor
inferred← citeshttps://doi.org/10.1529/biophysj.106.098095openalex-snapshot
Characterization of the Gating Conformational Changes in the Felbamate Binding Site in NMDA Channels
inferred← citeshttps://doi.org/10.1529/biophysj.106.103176openalex-snapshot
Extracellular Proton-Modulated Pore-Blocking Effect of the Anticonvulsant Felbamate on NMDA Channels
inferred← citeshttps://doi.org/10.17221/6265-vetmedopenalex-snapshot
The effect of felbamate on behavioural sensitization to methamphetamine in mice
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