| Literature DB >> 20804199 |
Paul A Glossop1, Charlotte A L Lane, David A Price, Mark E Bunnage, Russell A Lewthwaite, Kim James, Alan D Brown, Michael Yeadon, Christelle Perros-Huguet, Michael A Trevethick, Nicholas P Clarke, Robert Webster, Rhys M Jones, Jane L Burrows, Neil Feeder, Stefan C J Taylor, Fiona J Spence.
Abstract
A novel series of potent and selective sulfonamide derived β(2)-adrenoreceptor agonists are described that exhibit potential as inhaled ultra-long-acting bronchodilators for the treatment of asthma and chronic obstructive pulmonary disease. Analogues from this series mediate very long-lasting smooth muscle relaxation in guinea pig tracheal strips. The sulfonamide agonist headgroup confers high levels of intrinsic crystallinity that could relate to the acidic sulfonamide motif supporting a zwitterionic form in the solid state. Optimization of pharmacokinetic properties was achieved through targeted introduction of a phenolic moiety to support rapid phase II clearance, thereby minimizing systemic exposure following inhalation and reducing systemically mediated adverse events. Compound 38 (PF-610355) is identified as a clinical candidate from this series, with in vivo duration of action studies confirming its potential for once-daily use in humans. Compound 38 is currently in advanced phase II clinical studies.Entities:
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Year: 2010 PMID: 20804199 DOI: 10.1021/jm1005989
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 8.039