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Synthesis and Biological Activities of Novel 1,2,3,5-Tetrahydroimidazo[2,1-b]quinazoline Derivatives

机译:新型1,2,3,5-四氢咪唑并[2,1-b]喹唑啉衍生物的合成及生物活性

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摘要

A series of variously substituted 1,2,3,5-tetrahydroimidazo[2,1-b]quinazoline derivatives 3-4 and 6-7 were prepared by the reactions of 2-chloro-4,5-dihydroimidazole (1) with the appropriate 2-aminophenyl ketones 2 and 5.The structures of the new compounds obtained were determined by elemental analysis as well as IR and NMR spectroscopic data.Biological activities of the compounds 3 and 6 was examined on P_2 membrane preparations obtained from rat whole brains and rat tail artery.Among the compounds tested,5-methylidene-l,2,3,5-tetrahydroimidazo[2,l-b]quinazoline (6a) showed high and moderate binding affinities to I_2 imidazoline (KAPPA_i=5.2 nM) and alpha_2-adrenergic (KAPPA_i=149 nM) receptors,respectively.
机译:通过使2-氯-4,5-二氢咪唑(1)与2-氯-4,5-二氢咪唑(1)反应制得一系列不同取代的1,2,3,5-四氢咪唑并[2,1-b]喹唑啉衍生物3-4和6-7。适当的2-氨基苯基酮2和5.通过元素分析以及IR和NMR光谱数据确定了新化合物的结构。在从大鼠全脑和大脑中获得的P_2膜制剂上检查了化合物3和6的生物活性在测试的化合物中,5-亚甲基-1,2,3,5-四氢咪唑并[2,1b]喹唑啉(6a)对I_2咪唑啉(KAPPA_i = 5.2 nM)和α_2-肾上腺素能具有高和中等的结合亲和力(KAPPA_i = 149 nM)受体。

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