Publication | Open Access
BMS-933043, a Selective α7 nAChR Partial Agonist for the Treatment of Cognitive Deficits Associated with Schizophrenia
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Citations
32
References
2017
Year
NeuropsychologyPsychotropic MedicationSynaptic TransmissionNeurotransmitterPsychopharmacologyClinical NeuroscienceSynaptic SignalingSocial SciencesMolecular PharmacologyNeurologyCognitive NeuroscienceNeurochemistryMolecular NeurosciencePsychiatrySelective α7NeuropharmacologyPharmacologyPsychotic DisorderCognitive Deficits AssociatedCellular NeuroscienceCognitive DysfunctionSchizophreniaTherapeutic TreatmentNeuroscienceBiological PsychiatryNegative SymptomsMedicineReceptor AgonistsPartial Agonist
The therapeutic treatment of negative symptoms and cognitive dysfunction associated with schizophrenia is a significant unmet medical need. Preclinical literature indicates that α7 neuronal nicotinic acetylcholine (nACh) receptor agonists may provide an effective approach to treating cognitive dysfunction in schizophrenia. We report herein the discovery and evaluation of 1c (BMS-933043), a novel and potent α7 nACh receptor partial agonist with high selectivity against other nicotinic acetylcholine receptor subtypes (>100-fold) and the 5-HT3A receptor (>300-fold). In vivo activity was demonstrated in a preclinical model of cognitive impairment, mouse novel object recognition. BMS-933043 has completed Phase I clinical trials.
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