Department of Worldwide Medicinal Chemistry, Pfizer Global Research and Development, Sandwich Laboratories, Ramsgate Road, Kent CT139NJ, UK.
J Med Chem. 2010 Sep 23;53(18):6640-52. doi: 10.1021/jm1005989.
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.
描述了一系列新型强效和选择性磺酰胺衍生的β2-肾上腺素受体激动剂,它们具有作为吸入型超长效支气管扩张剂的潜力,用于治疗哮喘和慢性阻塞性肺疾病。该系列中的类似物介导豚鼠气管条非常持久的平滑肌松弛。磺酰胺激动剂头基团赋予高程度的固有结晶性,这可能与酸性磺酰胺基序在固体状态下支持两性离子形式有关。通过有针对性地引入酚部分来优化药代动力学特性,从而支持快速的 II 相清除,从而最小化吸入后的全身暴露并减少全身性介导的不良事件。该系列中的化合物 38 (PF-610355) 被确定为临床候选药物,其体内作用持续时间研究证实了其在人类中每日一次使用的潜力。化合物 38 目前正在进行先进的 II 期临床研究。