Szacoń Elżbieta, Rządkowska Marzena, Kaczor Agnieszka A, Kędzierska Ewa, Orzelska-Górka Jolanta, Fidecka Sylwia, Matosiuk Dariusz
Department of Synthesis and Chemical Technology of Pharmaceutical Substances with Computer Modeling Lab, Faculty of Pharmacy with Division of Medical Analytics, Medical University of Lublin, 4a Chodźki St., Lublin PL-20093, Poland.
School of Pharmacy, University of Eastern Finland, Yliopistonranta 1, P.O. Box 1627, Kuopio FI-70211, Finland.
Molecules. 2016 Apr 30;21(5):582. doi: 10.3390/molecules21050582.
Novel 1-(1,4-alkylaryldisubstituted-4,5-dihydro-1H-imidazo)-3-substituted urea derivatives have been synthesized and evaluated for their central nervous system activity. Compounds 3a-m were prepared in the reaction between the respective 1-alkyl-4-aryl-4,5-dihydro-1H-imidazol-2-amines 1a-c and appropriate isocyanates 2 in dichloromethane. The compounds were subjected to in silico ADMET studies in order to select best candidates for in vivo experiments. The effects of the compounds on the spontaneous locomotor activity and amphetamine-evoked hyperactivity were estimated. Analgesic activity, without or in the presence of naloxone, was assessed in the writhing test. The tendency to change the HTR, evoked by l-5-HTP and the involvement in alteration in body temperature in mice was studied. Additionally, to check possible occurrence of drug-induced changes in the muscle relaxant activity of mice, which may have contributed to their behaviour in other tests, the rota-rod and chimney tests were performed. The new urea derivatives exerted significant activities in the performed pharmacological tests, although the presented results show a preliminary estimation, and thus, need to be extended for identification and understanding the complete pharmacological profile of the examined compounds.
新型1-(1,4-烷基芳基二取代-4,5-二氢-1H-咪唑)-3-取代脲衍生物已被合成并评估其对中枢神经系统的活性。化合物3a-m是在二氯甲烷中,由相应的1-烷基-4-芳基-4,5-二氢-1H-咪唑-2-胺1a-c与合适的异氰酸酯2反应制备而成。为了选择体内实验的最佳候选化合物,对这些化合物进行了计算机辅助的ADMET研究。评估了这些化合物对自发运动活性和苯丙胺诱发的多动的影响。在扭体试验中评估了在有无纳洛酮存在下的镇痛活性。研究了由l-5-羟色氨酸诱发的5-羟色胺受体变化趋势以及对小鼠体温变化的影响。此外,为了检查药物诱导的小鼠肌肉松弛活性变化的可能性,这种变化可能影响了它们在其他试验中的行为,进行了转棒试验和烟囱试验。尽管所呈现的结果只是初步估计,但新的脲衍生物在进行的药理试验中表现出显著活性,因此,需要进一步扩展研究以确定和了解所研究化合物的完整药理特性。