301355-95-3Relevant articles and documents
Comparison of three γ-turn mimetic scaffolds incorporated into angiotensin II
Lindman, Susanna,Lindeberg, Gunnar,Nyberg, Fred,Karlen, Anders,Hallberg, Anders
, p. 2375 - 2383 (2000)
Rigidification of peptides by cyclization and iterative incorporation of well-defined secondary structure mimetics constitutes one approach to the design of non-peptidergic structures with better defined conformations. We herein present the synthesis of a potential γ-turn mimetic scaffold, and its incorporation in the 3-5 position of angiotensin II. Two analogues of angiotensin II (Ang II) incorporating this 1,3,5-trisubstituted benzene γ-turn scaffold were synthesized. Evaluation of the compounds in a radioligand binding assay showed that they lacked affinity to the AT1 receptor. To rationalize these results a geometrical and electrostatical comparison with Ang II analogues encompassing a bicyclic scaffold that delivered inactive pseudo peptides and an azepine scaffold producing highly active ligands was made. This analysis did not provide a clear rationale for the inactivity of the benzene γ-turn scaffolds. Copyright (C) 2000 Elsevier Science Ltd.
