| Literature DB >> 24900851 |
Michael J Stocks1, Lilian Alcaraz1, Andrew Bailey1, Roger Bonnert1, Elaine Cadogan1, Jadeen Christie1, John Dixon1, Stephen Connolly1, Anthony Cook1, Adrian Fisher1, Alice Flaherty1, Alexander Humphries1, Anthony Ingall1, Stephen Jordan1, Mandy Lawson1, Alex Mullen1, David Nicholls1, Stuart Paine1, Garry Pairaudeau1, Alan Young1.
Abstract
A series of dibasic des-hydroxy β2 receptor agonists has been prepared and evaluated for potential as inhaled ultralong acting bronchodilators. Determination of activities at the human β-adrenoreceptors demonstrated a series of highly potent and selective β2 receptor agonists that were progressed to further study in a guinea pig histamine-induced bronchoconstriction model. Following further assessment by onset studies in guinea pig tracheal rings and human bronchial rings contracted with methacholine (guinea pigs) or carbachol (humans), duration of action studies in guinea pigs after intratracheal (i.t.) administration and further selectivity and safety profiling AZD3199 was shown to have an excellent over all profile and was progressed into clinical evaluation as a new ultralong acting inhaled β2 receptor agonist with rapid onset of action.Entities:
Keywords: AZD3199; COPD; adrenoreceptor agonist; asthma; inhaled; uLABA; β2 receptor agonist
Year: 2014 PMID: 24900851 PMCID: PMC4027610 DOI: 10.1021/ml4005232
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345