https://www.selleckchem.com/products/tdi-011536.html Indeed, we observed faster RTs and greater representational similarity for primed than unprimed trials, suggesting that mental representations of abstract relations are transiently activated on this incidental analogy task. Finally, we found a significant correlation between behavioral and neural priming across participants. To our knowledge, this is the first study to investigate relational priming using functional neuroimaging and to show that neural representations are strengthened by relational priming. This research shows how abstract concepts can be brought to mind momentarily, even when not required for task performance. Antiseizure drugs (ASDs) play a central and crucial role in the treatment of epilepsy patients because the majority require anticonvulsant treatment for an extended period of time. Due to the fact that 30% of patients are refractory to medical treatment, new therapeutic options are necessary. Cenobamate is the latest approved antiepileptic drug in focal epilepsy, and its mode of action is thought to be mediated by blocking voltage-gated sodium channels and interaction with the GABAergic system. This article reviews animal studies, pharmacokinetics, pharmacodynamics, and the phase 1 to 3 trials and open-label extension data on cenobamate. Cenobamate has the potential to perform as an important ASD because trial data are indicative of remarkable responder and seizure freedom rates so far not seen with other ASDs. Cenobamate demonstrated significant efficacy at a dosage between 100 and 400mg per day. The side-effect profile of this drug is comparable to other ASDs and is mainly CNS related; in particular, somnolence, dizziness, headache, diplopia, and nystagmus. However, slow titration is mandatory to decrease the risk of drug rash with eosinophilia and systemic symptoms (DRESS) that was observed in several patients with fast uptitration schemes. Cenobamate has the potential to perform as an i