Professor JILLIAN BAKER jillian.baker@nottingham.ac.uk
PROFESSOR OF DRUG DISCOVERY AND RESPIRATORY MEDICINE
Novel selective β1-adrenoceptor antagonists for concomitant cardiovascular and respiratory disease
Baker, Jillian G.; Gardiner, Sheila M.; Woolard, Jeanette; Fromont, Christophe; Jadhav, Gopal P.; Mistry, Shailesh N.; Thompson, Kevin S.J.; Kellam, Barrie; Hill, Stephen J.; Fischer, Peter M.
Authors
Sheila M. Gardiner
Professor JEANETTE WOOLARD Jeanette.Woolard@nottingham.ac.uk
PROFESSOR OF CARDIOVASCULAR PHYSIOLOGY AND PHARMACOLOGY
Christophe Fromont
Gopal P. Jadhav
Dr SHAILESH MISTRY Shailesh.Mistry@nottingham.ac.uk
ASSOCIATE PROFESSOR
Kevin S.J. Thompson
Professor BARRIE KELLAM BARRIE.KELLAM@NOTTINGHAM.AC.UK
Head of School (Professor of Medicinal Chemistry)
Professor STEPHEN HILL STEVE.HILL@NOTTINGHAM.AC.UK
PROFESSOR OF MOLECULAR PHARMACOLOGY
Peter M. Fischer
Abstract
β-Blockers reduce mortality and improve symptoms in people with heart disease. However, current clinically available β-blockers have poor selectivity for the cardiac β1-adrenoceptor (AR) over the lung β2-AR. Unwanted β2-blockade risks causing life-threatening bronchospasm and a reduction in the efficacy of β2-agonist emergency rescue therapy. Thus current life-prolonging β-blockers are contraindicated in people with both heart disease and asthma. Here we describe NDD-713 and NDD-825, novel highly β1-selective neutral antagonists with good pharmaceutical properties that can potentially overcome this limitation. Radioligand binding studies and functional assays using human receptors expressed in CHO cells demonstrate that NDD-713 and NDD-825 have nanomolar β1-AR affinity, greater than 500-fold β1-AR vs β2-AR selectivity and no agonism. Studies in conscious rats demonstrated that they are orally bioavailable and cause pronounced β1-mediated reduction of heart rate while showing no effect on β2-mediated hindquarters vasodilatation. The compounds also have good disposition properties and show no adverse toxicological effects. They potentially offer a truly cardioselective β-blocker therapy for the large number of people with heart and respiratory, or peripheral vascular comorbidities.
Citation
Baker, J. G., Gardiner, S. M., Woolard, J., Fromont, C., Jadhav, G. P., Mistry, S. N., Thompson, K. S., Kellam, B., Hill, S. J., & Fischer, P. M. (2017). Novel selective β1-adrenoceptor antagonists for concomitant cardiovascular and respiratory disease. FASEB Journal, 31(7), 3150-3166. https://doi.org/10.1096/fj.201601305R
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 20, 2017 |
Online Publication Date | Apr 11, 2017 |
Publication Date | Jul 31, 2017 |
Deposit Date | Mar 28, 2017 |
Publicly Available Date | Apr 11, 2017 |
Journal | FASEB Journal |
Print ISSN | 0892-6638 |
Electronic ISSN | 1530-6860 |
Publisher | Federation of American Society of Experimental Biology (FASEB) |
Peer Reviewed | Peer Reviewed |
Volume | 31 |
Issue | 7 |
Pages | 3150-3166 |
DOI | https://doi.org/10.1096/fj.201601305R |
Keywords | β-blocker, Selectivity, Heart disease, Asthma |
Public URL | https://nottingham-repository.worktribe.com/output/874855 |
Publisher URL | http://www.fasebj.org/content/31/7/3150 |
Contract Date | Mar 28, 2017 |
Files
3150.full.pdf
(2.7 Mb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/
You might also like
A novel and selective fluorescent ligand for the study of adenosine A2B receptors
(2024)
Journal Article
Downloadable Citations
About Repository@Nottingham
Administrator e-mail: discovery-access-systems@nottingham.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2025
Advanced Search