Department of Pulmonary Diseases Research, Boehringer Ingelheim Pharma GmbH & Co. KG, 88397 Biberach, Germany.
Bioorg Med Chem Lett. 2010 Feb 15;20(4):1410-4. doi: 10.1016/j.bmcl.2009.12.087. Epub 2010 Jan 4.
Compound 4p was identified from a series of 6-hydroxy-4H-benzo[1,4]oxazin-3-ones as potent agonist of the human beta2-adrenoceptor with a high beta1/beta2-selectivity. A complete reversal of acetylcholine-induced bronchoconstriction which lasted over the whole study period of 5h was demonstrated for 4p in a guinea pig in vivo model without any signs of cardiovascular effects up to 10-fold above the first dose reaching 100% bronchoprotection. The enantiomerically pure (R)-form of 4p exerted a bronchodilatory efficacy over 24 h in dogs and guinea pigs in the absence of systemic pharmacodynamic effects. Formoterol which was tested as comparator in the same in vivo models of acetylcholine-induced bronchoconstriction did not retain efficacy after 24 h. In summary, the preclinical profile of compound (R)-4p (olodaterol, also known as BI 1744 CL) suggests a potential for once-daily dosing in man accompanied with an improved safety profile.
化合物 4p 是从一系列 6-羟基-4H-苯并[1,4]恶嗪-3-酮中鉴定出来的,作为人β2-肾上腺素受体的有效激动剂,具有很高的β1/β2 选择性。在豚鼠体内模型中,4p 完全逆转了乙酰胆碱引起的支气管收缩,持续了整个 5 小时的研究期,而心血管作用的迹象在达到 10 倍于第一剂量的 100%支气管保护作用时也没有出现。在没有全身药效学作用的情况下,化合物 4p 的对映体纯(R)形式在狗和豚鼠中表现出超过 24 小时的支气管扩张作用。在相同的乙酰胆碱引起的支气管收缩的体内模型中作为对照药物进行测试的福莫特罗在 24 小时后没有保留疗效。总之,化合物(R)-4p(奥洛达特罗,也称为 BI 1744 CL)的临床前特征表明,在人体中可能每天给药一次,并具有改善的安全性特征。