Heterodimeric Analogues of the Potent Y1R Antagonist 1229U91, Lacking One of the Pharmacophoric C-Terminal Structures, Retain Potent Y1R Affinity and Show Improved Selectivity over Y4R
Rachel Richardson(Queen's Medical Centre), Philip E. Thompson(Molecular Research Institute), Marleen Groenen(University of Nottingham), Nicholas D. Holliday(University of Nottingham), Stephen J. Briddon(University of Nottingham), Mengjie Liu(Henan University), Simon J. Mountford
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