作者
Andrew D. Cansfield,Mark A. Ator,Joydeep Banerjee,Michael Bestwick,Andrea Bortolato,Giles A. Brown,Jason Brown,Kristina Butković,Julie E. Cansfield,J.A. Christopher,Miles Congreve,G. Cseke,Francesca Deflorian,Benjamin J. Dugan,Martina Petrović,Antun Hutinec,Trinadh Kumar Inturi,Goran Landek,Jonathan Mason,Alistair O’Brien,Gregory R. Ott,Renata Rupčić,Gordon Saxty,Stacey M. Southall,Rahela Zadravec,Stephen P. Watson
摘要
A series of macrocyclic calcitonin gene-related peptide (CGRP) receptor antagonists identified using structure-based design principles, exemplified by HTL0028016 (1) and HTL0028125 (2), is described. Structural characterization by X-ray crystallography of the interaction of two of the macrocycle antagonists with the CGRP receptor ectodomain is described, along with structure–activity relationships associated with point changes to the macrocyclic antagonists. The identification of non-peptidic/natural product-derived, macrocyclic ligands for a G protein coupled receptor (GPCR) is noteworthy.