Abstract

Through iterative design cycles we have discovered a number of novel new classes where the imidazo[1,5- a][1,2,4]-triazolo[1,5- d][1,4]benzodiazepine was deemed the most promising GABA A α5 inverse agonist class with potential for cognitive enhancement. This class combines a modest subtype binding selectivity with inverse agonism and has the most favourable molecular properties for further lead optimisation towards a central nervous system (CNS) acting medicine.

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