申请人:The Regents of The University of California
公开号:US05627169A1
公开(公告)日:1997-05-06
Novel phosphinic and phosphonic acid derivatives of pyridine, pyrrole and azepine with utility as antagonists of the GABA.sub.rho receptor are disclosed. These compounds have utility as modulators of the excitability of the central nervous system as mediated by their ability to specifically act on closed-channel binding sites of GABA.sub.rho receptors.
本发明揭示了吡啶、吡咯和杂环戊二磷和膦酸衍生物,其作为GABA.sub.rho受体的拮抗剂具有实用性。这些化合物作为中枢神经系统兴奋性调节剂具有实用性,通过它们特异地作用于GABA.sub.rho受体的闭合通道结合位点来介导中枢神经系统的兴奋性。