A class of 4-hydroxy-2-(1 H)-quinolone derivatives, substituted at the 3-position by an optionally substituted aryl substituent, are selective non-competitive antagonists of NMDA receptors and/or are antagonists of AMPA receptors, and are therefore of utility in the treatment of conditions, such as neurodegenerative disorders, convulsions or schizophrenia, which require the administration of an NMDA and/or AMPA receptor antagonist.
一类
4-羟基-2-(1H)-
喹诺酮衍
生物在 3 位被任选取代的芳基取代基取代,是 N
MDA 受体的选择性非竞争性拮抗剂和/或
AMPA 受体的拮抗剂,因此可用于治疗神经退行性疾病、惊厥或精神分裂症等需要施用 N
MDA 和/或
AMPA 受体拮抗剂的疾病。