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Elsevier, Bioorganic and Medicinal Chemistry, 6(9), p. 1639-1647, 2001

DOI: 10.1016/s0968-0896(01)00059-1

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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

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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