A series of quinoline and quinoxaline derivatives, substituted by a fused bicyclic pyridine or pyrimidine moiety attached via an alkylene chain optionally linked to a heteroatom, being selective inhibitors of P13 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,通过一个可选连接到杂原子的烷基链连接的融合双环
吡啶或
嘧啶基团进行取代,是选择性
PI3激酶酶
抑制剂,在医学中具有益处,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。