化学
卵清蛋白
药理学
贾纳斯激酶
激酶
信号转导
炎症
哮喘
细胞因子
酶抑制剂
肺
Janus激酶3
罗氟司特
酶
气道
促炎细胞因子
蛋白激酶A
蛋白激酶C
作用机理
丝裂原活化蛋白激酶
广告
支气管收缩
作者
Jordi Bach,Daniel Perez,Cristina Esteve,Oriol Llera,Lorena Taboada,Paul Eastwood,Jacob González,Lluı́s Pagès,Blanca López,Rosario Ramón,Laura Grau,Alberto Ortega,Alfredo González,Francesc Biosca,Jordi Serrat,Stephen Connolly,Silvia Fonquerna,Paul Beswick,Jordi Gràcia,Estrella Lozoya
标识
DOI:10.1021/acs.jmedchem.6c00169
摘要
Abstract Relevant cytokines involved in inflammatory processes in asthma and Chronic Obstructive Pulmonary Disease (COPD) signal through the Janus kinase (JAK) proteins. Therefore, a JAK inhibitor blocking multiple cytokine signaling pathways constitutes a potential new anti-inflammatory therapy for these diseases. Herein is described the discovery and progression of a novel series of pyrazolo[1,5-a]pyridine JAK inhibitors with a profile suitable for inhaled administration. Structural biology-guided design was used to improve potency, kinase selectivity, and lung retention of initial compounds, leading to the identification of compound 18 (LAS194046), a potent and selective pan-JAK inhibitor with an excellent profile for inhaled administration and proven efficacy in the ovalbumin (OVA)-induced airway inflammation model in rat by the inhaled route. As part of the optimization process leading to 18, the relevance of several physicochemical properties in lung retention has also been analyzed.
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