A series of quinoline and quinoxaline derivatives, substituted by an optionally substituted bicyclic heteroaryl moiety consisting of two fused six-membered aromatic rings attached via an alkylene chain optionally linked to a heteroatom, being selective inhibitors of PI3 kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions.
一系列
喹啉和
喹喔啉衍
生物,被一个可选取代的双环杂环芳基基团取代,该基团由两个融合的六元芳环通过一个可选连接到杂原子的烷基链连接而成,这些衍
生物是
PI3激酶酶的选择性
抑制剂,在医学上具有益处,例如用于治疗炎症、自身免疫、心血管、神经退行性、代谢、肿瘤、疼痛或眼科疾病。