Rational Drug Design and Synthesis of Molecules Targeting the Angiotensin II Type 1 and Type 2 Receptors (original) (raw)

Development of angiotensin II antagonists with equipotent affinity for human AT1 and AT2 receptor subtypes

Tomasz Glinka

Bioorganic & Medicinal Chemistry Letters, 1994

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Superimposition of potent non-peptide AT1 receptor antagonists with angiotensin II

John Matsoukas

Letters in Peptide Science, 1996

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N- and C-terminal structure–activity study of angiotensin II on the angiotensin AT2 receptor

Lenka Rihakova

European Journal of Pharmacology, 1998

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Leveraging NMR and X-ray Data of the Free Ligands to Build Better Drugs Targeting Angiotensin II Type 1 G-Protein Coupled Receptor

Maria Zervou

Current Medicinal Chemistry, 2015

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The design, binding affinity prediction and synthesis of macrocyclic angiotensin II AT1 and AT2 receptor antagonists

Tomasz Glinka

Bioorganic & Medicinal Chemistry Letters, 1996

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A single beta-amino acid substitution to angiotensin II confers AT2 receptor selectivity and vascular function

Emma Jones, Daniel Clayton

Hypertension, 2011

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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

John Matsoukas

Bioorganic & Medicinal Chemistry, 2001

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Angiotensin II cyclic analogs as tools to investigate AT1R biased signaling mechanisms

Pierre Lavigne

Biochemical Pharmacology, 2018

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Compound 21, the first orally active, selective agonist of the angiotensin type 2 receptor (AT2): implications for AT2 receptor research and therapeutic potential

Thomas Unger

Journal of the Renin-Angiotensin-Aldosterone System, 2009

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Structural basis for selectivity and diversity in angiotensin II receptors

Nilkanth Patel

Nature, 2017

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Selective angiotensin II AT2 receptor agonists: Benzamide structure–activity relationships

Fred Nyberg, Nicole Gallo-payet, Ulrika Rosenström, Mathias Hallberg

Bioorganic & Medicinal Chemistry, 2008

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Design, synthesis, and antihypertensive evaluation of 2′-tetrazolyl and 2′-carboxy-biphenylylmethyl-pyrrolidine scaffolds substituted at their N1, C3, and C4 positions as potential angiotensin II AT1 receptor antagonists

Nasser Ismail

Medicinal Chemistry Research, 2014

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Angiotensin II Pseudopeptides Containing 1,3,5-Trisubstituted Benzene Scaffolds with High AT 2 Receptor Affinity

Adolf Gogoll, Mats Larhed, Gunnar Lindeberg, Fred Nyberg

Journal of Medicinal Chemistry, 2005

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Structural determinants for binding to angiotensin converting enzyme 2 (ACE2) and angiotensin receptors 1 and 2

Daniel Clayton

Frontiers in Pharmacology, 2015

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Molecular Mechanism Underlying Inverse Agonist of Angiotensin II Type 1 Receptor

Yoshinari Uehara

Journal of Biological Chemistry, 2006

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Structural Insight on the Activity of Type 1 Angiotensin II Peptide Antagonists Using MD Simulations

Hernâni Maia

The Journal of Physical Chemistry B, 2008

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Nanotechnology and Membrane Receptors: Focus on Angiotensin II Receptors

Guang Li

Medical Clinics of North America, 2007

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Structural Basis for Ligand Recognition and Functional Selectivity at Angiotensin Receptor

Nilkanth Patel

The Journal of biological chemistry, 2015

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Design, Synthesis, Structural Studies, Biological Evaluation, and Computational Simulations of Novel Potent AT 1 Angiotensin II Receptor Antagonists Based on the 4-Phenylquinoline Structure

Maurizio Anzini

Journal of Medicinal Chemistry, 2004

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Update on Angiotensin II Subtype 2 Receptor: Focus on Peptide and Nonpeptide Agonists

Ali Aghazadeh-Habashi

Molecular Pharmacology, 2021

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Emerging Concepts of Regulation of Angiotensin II Receptors

Eugene Patkin

Arteriosclerosis, Thrombosis, and Vascular Biology, 2007

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The Second Transmembrane Domain of the Human Type 1 Angiotensin II Receptor Participates in the Formation of the Ligand Binding Pocket and Undergoes Integral Pivoting Movement during the Process of Receptor Activation

Richard Leduc, Pierre Lavigne

Journal of Biological Chemistry, 2009

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Conformational and biological studies for a pair of novel synthetic AT1 antagonists: stereoelectronic requirements for antihypertensive efficacy

Panagiotis Zoumpoulakis

Journal of Pharmaceutical and Biomedical Analysis, 2003

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Design, synthesis and biological evaluation of cyclic angiotensin II analogues with 3, 5 side-chain bridges: role of C-terminal aromatic residue and ring cluster for activity and implications in the drug design of AT1 non-peptide antagonists

Panagiotis Zoumpoulakis

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Nonpeptidic angiotensin II AT1 receptor antagonists derived from 6-substituted aminocarbonyl and acylamino benzimidazoles

Fan Fei

European Journal of Medicinal Chemistry, 2013

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Receptor interactions of the position 4 side chains of angiotensin II analogues: Importance of aromatic ring quadrupole

John Matsoukas

Journal of Molecular Recognition, 1994

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In vitro pharmacological characterization of a new selective angiotensin AT1 receptor antagonist, UR-7280

Julian Garcia

European Journal of Pharmacology, 1996

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The Angiotensin II AT1 Receptor Structure-Activity Correlations in the Light of Rhodopsin Structure

Clovis Nakaie

Physiological Reviews, 2007

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An update on non-peptide angiotensin receptor antagonists and related RAAS modulators

Mrs. Rupinder Sodhi

Life Sciences, 2007

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Distinctions between non-peptide angiotensin II AT1-receptor antagonists

Frederik Fierens

Journal of the Renin-Angiotensin-Aldosterone System, 2001

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Angiotensin II receptor type 1 (AT1) selective nonpeptidic antagonists—A perspective

Prashant Naik, Mange Ram Yadav

Bioorganic & Medicinal Chemistry, 2010

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Design and synthesis of novel antihypertensive drugs

P. Moutevelis-minakakis

Bioorganic & Medicinal Chemistry Letters, 2003

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The design and synthesis of a potent angiotensin II cyclic analogue confirms the ring cluster receptor conformation of the hormone angiotensin II

John Matsoukas

Bioorganic & Medicinal Chemistry, 2000

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