Synthesis and in vitro muscarinic activities of a Series of 1,3-diazacycloalkyl carboxaldehyde oxime derivatives
作者:Ralf Plate、Christan G.J.M Jans、Marc J.M Plaum、Thijs de Boer
DOI:10.1016/s0968-0896(01)00379-0
日期:2002.4
tested for muscarinic activity in receptor binding assays using [3H]-oxotremorine-M (OXO-M) and [3H]-pirenzepine (PZ) as ligands. Potential muscarinic agonistic or antagonistic properties of the compounds were determined using binding studies measuring their potencies to inhibit the binding of OXO-M and PZ. Preferential inhibition of OXO-M binding was used as an indicator for potential muscarinic agonistic
合成了一系列的1,3-二氮杂环烷基羧醛肟衍生物,并以[3H]-氧代脱氢吗啡-M(OXO-M)和[3H]-哌仑西平(PZ)作为配体,在受体结合测定中测试了毒蕈碱活性。使用结合研究确定化合物的潜在毒蕈碱激动或拮抗特性,该研究测量了其抑制OXO-M和PZ结合的能力。OXO-M结合的优先抑制被用作潜在的毒蕈碱激动特性的指标;在隔离器官的功能研究中证实了这种潜力。