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Title: Sigma-1 ligands: Tic-hydantoin as a key pharmacophore. Author: Toussaint M, Mousset D, Foulon C, Jacquemard U, Vaccher C, Melnyk P. Journal: Eur J Med Chem; 2010 Jan; 45(1):256-63. PubMed ID: 19875205. Abstract: Sigma-1 receptors are involved in numerous pathological dysfunctions and the synthesis of selective ligands is of interest. We identified a fused tetrahydroisoquinoline-hydantoin (Tic-hydantoin) structure with high affinity and selectivity for these receptors. We report here our efforts towards the pharmacomodulation of this substructure, the synthesis of 9 analogs with stereochemistry inversion, opening of isoquinoline ring, removal of isoquinoline nitrogen, replacement of isoquinoline by pyridine, of Tic-hydantoin moiety by quinazolinedione heterocycle. All these analogs provided a loss in the affinity for the sigma-1 receptor. The present work underlines the real importance of the Tic-hydantoin moiety for the obtainment of high affinity ligands.[Abstract] [Full Text] [Related] [New Search]