Optimisation of a series of potent, selective and orally bioavailable GlyT1 inhibitors
                                
                                    
                                        作者:Joanne L. Thomson、Wesley P. Blackaby、Andrew S.R. Jennings、Simon C. Goodacre、Andrew Pike、Steve Thomas、Terry A. Brown、Alison Smith、Gopalan Pillai、Leslie J. Street、Richard T. Lewis                                    
                                    
                                        DOI:10.1016/j.bmcl.2009.02.102
                                    
                                    
                                        日期:2009.4
                                    
                                    A series of heterocyclic sulfonamides have been developed which are potent and selective inhibitors of hGlyT1. SAR studies to optimise the in vitro and in vivo properties are described. Optimisation of the central scaffold resulted in cyclohexane sulfones 28 and 29, which have good PK properties and show promise for further development. (c) 2009 Elsevier Ltd. All rights reserved.