丙酸氟替卡松
药理学
化学
吸入
药品
糖皮质激素受体
肺
兴奋剂
水肿
糖皮质激素
医学
麻醉
受体
内科学
生物化学
作者
Martin Hemmerling,Stinabritt Nilsson,K. A. P. Edman,Stefan Eirefelt,Wayne L. Russell,Ramon Hendrickx,Eskil Johnsson,Carina Kärrman Mårdh,Markus Berger,Hartmut Rehwinkel,Anna Abrahamsson,Jan Dahmén,Anders Eriksson,Bálint Gábos,Krister Henriksson,Nafizal Hossain,Svetlana Ivanova,Anne‐Helene Jansson,Tina Jellesmark Jensen,Anders Jerre
标识
DOI:10.1021/acs.jmedchem.7b01215
摘要
A class of potent, nonsteroidal, selective indazole ether-based glucocorticoid receptor modulators (SGRMs) was developed for the inhaled treatment of respiratory diseases. Starting from an orally available compound with demonstrated anti-inflammatory activity in rat, a soft-drug strategy was implemented to ensure rapid elimination of drug candidates to minimize systemic GR activation. The first clinical candidate 1b (AZD5423) displayed a potent inhibition of lung edema in a rat model of allergic airway inflammation following dry powder inhalation combined with a moderate systemic GR-effect, assessed as thymic involution. Further optimization of inhaled drug properties provided a second, equally potent, candidate, 15m (AZD7594), that demonstrated an improved therapeutic ratio over the benchmark inhaled corticosteroid 3 (fluticasone propionate) and prolonged the inhibition of lung edema, indicating potential for once-daily treatment.
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