Stabilization of Angiotensin-(1–7) by key substitution with a cyclic non-natural amino acid-Reference-Cited by-同舟云学术

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Stabilization of Angiotensin-(1–7) by key substitution with a cyclic non-natural amino acid

Published:2017-07-25 Issue:10 Volume:49 Page:1733-1742
ISSN:0939-4451
Container-title:Amino Acids
language:en
Short-container-title:Amino Acids

Author:

Wester Anita,Devocelle Marc,Tallant E. Ann,Chappell Mark C.,Gallagher Patricia E.,Paradisi Francesca^ORCID

Funder

Science Foundation Ireland

National University of Ireland

National Institutes of Health

American Heart Association

Randi B. Weiss Cancer Research Fund

Farley-Hudson Foundation

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Clinical Biochemistry,Biochemistry

Link

http://link.springer.com/article/10.1007/s00726-017-2471-9/fulltext.html

Reference25 articles.

1. Chappell MC (2016) Biochemical evaluation of the renin-angiotensin system: the good, bad, and absolute? Am J Physiol Heart Circ Physiol 310:H137–H152

2. Chappell MC, Pirro NT, Sykes A, Ferrario CM (1998) Metabolism of angiotensin-(1–7) by angiotensin-converting enzyme. Hypertension 31:362–367

3. Cook KL, Metheny-Barlow LJ, Tallant EA, Gallagher PE (2010) Angiotensin-(1–7) reduces fibrosis in orthotopic breast tumors. Cancer Res 70:8319–8328

4. Cruz-Diaz N, Wilson BA, Pirro NT, Brosnihan KB, Marshall AC, Chappell MC (2016) Identification of dipeptidyl peptidase 3 as the angiotensin-(1–7) degrading peptidase in human HK-2 renal epithelial cells. Peptides 83:29–37

5. Fraga-Silva RA, Costa-Fraga FP, De Sousa FB, Alenina N, Bader M, Sinisterra RD, Santos RA (2011) An orally active formulation of angiotensin-(1–7) produces an antithrombotic effect. Clinics 66:837–841

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