Multiparameter Optimization in CNS Drug Discovery: Design of Pyrimido[4,5- <i>d</i> ]azepines as Potent 5-Hydroxytryptamine 2C (5-HT _2C ) Receptor Agonists with Exquisite Functional Selectivity over 5-HT _2A and 5-HT _2B Receptors

Abstract

A series of 4-substituted pyrimido[4,5-d]azepines that are potent, selective 5-HT2C receptor partial agonists is described. A rational medicinal chemistry design strategy to deliver CNS penetration coupled with SAR-based optimization of selectivity and agonist potency provided compounds with the desired balance of preclinical properties. Lead compounds 17 (PF-4479745) and 18 (PF-4522654) displayed robust pharmacology in a preclinical canine model of stress urinary incontinence (SUI) and no measurable functional agonism at the key selectivity targets 5-HT2A and 5-HT2B in relevant tissue-based assay systems. Utilizing recent advances in the structural biology of GPCRs, homology modeling has been carried out to rationalize binding and agonist efficacy of these compounds.