Angiotensin Analogues Palmitoylated in Positions 1 and 4
Author:
Affiliation:
1. Département de Pharmacologie, Faculté de Médecine, Université de Sherbrooke, Sherbrooke, Québec J1H 5N4, Canada
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm9608669
Reference60 articles.
1. Pérodin, J.; Bossé, R.; Gagnon, S.; Zhou, L.M.; Bouley, R.; Leduc, R.; Escher, E. Structure-activity Relationship of the Agonist-antagonist Transition on the Type 1 Angiotensin II Receptor; the Search for Inverse Agonists. InRecent Advances in Cellular and Molecular Aspects ofAngiotensin Receptors; Raizada, M. K., Phillips, M. I., Summers, C., Eds.; Plenum Press: New York, 1996; Vol. 358, pp 131−143.
2. Angiotensin-II Analogues. I: Synthesis and incorporation of the halogenated amino acids 3-(4?-iodophenyl)alanine, 3-(3?,5?-dibromo-4?-chlorophenyl)alanine, 3-(3?,4?,5?-tribromophenyl)alanine, and 3-(2?,3?,4?,5?,6?-pentabromophenyl)alanine
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