Rational design, synthesis, and structure–activity relationship of benzoxazolones: New potent mglu5 receptor antagonists based on the fenobam structure
作者:Simona M. Ceccarelli、Georg Jaeschke、Bernd Buettelmann、Jörg Huwyler、Sabine Kolczewski、Jens-Uwe Peters、Eric Prinssen、Richard Porter、Will Spooren、Eric Vieira
DOI:10.1016/j.bmcl.2006.12.006
日期:2007.3
A novel class of potent and stable mGlu5 receptor antagonists was developed by combining information from a high-throughput screening campaign with the structure of the known anxiolytic fenobam. Representative compounds from this class show favorable pharmacokinetic properties and are active in an in vivo model of anxiety.
通过将来自高通量筛选活动的信息与已知的抗焦虑性芬巴胺的结构相结合,开发出了一类新型的有效且稳定的mGlu5受体拮抗剂。该类别的代表性化合物表现出有利的药代动力学性质,并且在体内焦虑模型中具有活性。