Optimized glucuronidation of dual pharmacology β-2 agonists/M3 antagonists for the treatment of COPD-Reference-Cited by-同舟云学术

Optimized glucuronidation of dual pharmacology β-2 agonists/M3 antagonists for the treatment of COPD

Published:2011 Issue:9 Volume:2 Page:870
ISSN:2040-2503
Container-title:MedChemComm
language:en
Short-container-title:Med. Chem. Commun.

Author:

Hilton Laura,Osborne Rachel,Kenyon Amy S.,Baldock Helen,Bunnage Mark E.,Burrows Jane,Clarke Nick,Coghlan Michele,Entwistle David,Fairman David,Feeder Neil,James Kim,Jones Rhys M.,Laouar Nadia,Lunn Graham,Marshall Stuart,Newman Sandra D.,Patel Sheena,Selby Matthew D.,Spence Fiona,Stuart Emilio F.,Summerhill Susan,Trevethick Michael A.,Wright Karen N.,Yeadon Michael,Price David A.,Jones Lyn H.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pharmaceutical Science,Biochemistry,Drug Discovery,Molecular Medicine,Pharmacology,Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2011/MD/C1MD00140J

Reference22 articles.

1. The scientific rationale for combining long-acting β2-agonists and muscarinic antagonists in COPD

2. Optimising treatment for COPD - new strategies for combination therapy

3. Muscarinic antagonist-β-adrenergic agonist dual pharmacology molecules as bronchodilators: a patent review

4. Novel long-acting bronchodilators for COPD and asthma

5. Inhalation by design: Dual pharmacology β-2 agonists/M3 antagonists for the treatment of COPD

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