Synthesis and study of a cyclic angiotensin II antagonist analogue reveals the role of π*-π* interactions in the C-terminal aromatic residue for agonist activity and its structure resemblance with AT1 non-peptide antagonists

Citation:

Polevaya, L. ; Mavromoustakos, T. ; Zoumboulakis, P. ; Grdadolnik, S. G. ; Roumelioti, P. ; Giatas, N. ; Mutule, I. ; Keivish, T. ; Vlahakos, D. V. ; Iliodromitis, E. K. ; et al. Synthesis And Study Of A Cyclic Angiotensin Ii Antagonist Analogue Reveals The Role Of Π*-Π* Interactions In The C-Terminal Aromatic Residue For Agonist Activity And Its Structure Resemblance With At1 Non-Peptide Antagonists. Bioorganic and Medicinal Chemistry 2001, 9, 1639 - 1647.

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Cited By :25Export Date: 23 August 2017

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