Ciechanowicz-Rutkowska M, Oleksyn B J, Suszko-Purzycka A, Lipińska T
Regional Laboratory of Physicochemical Analysis and Structural Research, Jagiellonian University, Kraków, Poland.
J Pharm Sci. 1992 Jun;81(6):559-64. doi: 10.1002/jps.2600810619.
The synthesis, spectroscopic characteristics, and single-crystal X-ray structural analysis of quitenidine methyl ester monohydrate, a derivative of the muscarinic antagonist quinidine, are presented. Quitenidine methyl ester monohydrate (C20H24N2O4.H2O) crystallizes in the orthorhombic space group P2(1)2(1)2(1), with a = 16.69(3) A, b = 12.46(2) A, c = 9.70(1) A, and Z = 4. The crystal structure was refined to a discrepancy factor (R) of 0.097. Substitution of the quinidine vinyl chain with a carboxymethyl group does not influence the conformation. The carboxymethyl group is positionally disordered, a fact that complicates refinement of the structure. The water molecule is bonded to the quinuclidine nitrogen atom, and the hydroxyl group forms an intermolecular hydrogen bond with the quinoline nitrogen atom. The molecular structure of the ester was compared with those of quinidine, quinine, and four other antimuscarinic agents. An approximately linear relationship between the distance from the nonaromatic nitrogen to the plane of the aromatic part of the molecules and the blocking potency of these agents was noted; the greater this distance, the more potent is the antagonist.
本文介绍了毒蕈碱拮抗剂奎尼丁的衍生物喹替尼定甲酯一水合物的合成、光谱特性及单晶X射线结构分析。喹替尼定甲酯一水合物(C20H24N2O4·H2O)结晶于正交晶系空间群P2(1)2(1)2(1)中,a = 16.69(3) Å,b = 12.46(2) Å,c = 9.70(1) Å,Z = 4。晶体结构精修后的偏离因子(R)为0.097。用羧甲基取代奎尼丁的乙烯基链不影响其构象。羧甲基在位置上无序,这一事实使结构精修变得复杂。水分子与奎宁环氮原子相连,羟基与喹啉氮原子形成分子间氢键。将该酯的分子结构与奎尼丁、奎宁及其他四种抗毒蕈碱剂的结构进行了比较。注意到从非芳香氮到分子芳香部分平面的距离与这些药剂的阻断效力之间存在近似线性关系;该距离越大,拮抗剂的效力越强。