College of Pharmacy, Liaocheng University, Liaocheng 252059, China.
College of Life Sciences, Liaocheng University, Liaocheng 252059, China.
Molecules. 2019 May 14;24(10):1857. doi: 10.3390/molecules24101857.
In this study, we synthetized a series of 5-aryl-4,5-dihydrotetrazolo[1,5-]thieno[2,3-]pyridine derivatives containing tetrazole and other heterocycle substituents, i.e., triazole, methyltriazole, and triazolone. The forced swim test (FST) and tail suspension test (TST) were used to evaluate the antidepressant activity of the target compounds. The compound 5-[4-(trifluoromethyl)phenyl]-4,5-dihydrotetrazolo[1,5-]thieno[2,3-]pyridine () showed the highest antidepressant activity, with a reduced immobility time of 55.33% when compared with the control group. Using an open-field test, compound was shown to not affect spontaneous activity of mice. The determination of in vivo 5-hydroxytryptamine (5-HT) concentration showed that compound may have an effect in the mouse brain. The biological activities of all synthetized compounds were verified by molecular docking studies. Compound showed significant interactions with residues of the 5-HT receptor homology model.
在这项研究中,我们合成了一系列含有三唑和其他杂环取代基的 5-芳基-4,5-二氢四唑并[1,5-a]噻吩并[2,3-d]嘧啶衍生物,如三唑、甲基三唑和三唑酮。采用强迫游泳试验(FST)和悬尾试验(TST)评估目标化合物的抗抑郁活性。化合物 5-[4-(三氟甲基)苯基]-4,5-二氢四唑并[1,5-a]噻吩并[2,3-d]嘧啶()表现出最高的抗抑郁活性,与对照组相比,其不动时间减少了 55.33%。通过开放式试验,证明化合物对小鼠的自发活动没有影响。体内 5-羟色胺(5-HT)浓度的测定表明,化合物可能对小鼠大脑有作用。通过分子对接研究验证了所有合成化合物的生物活性。化合物与 5-HT 受体同源模型的残基表现出显著的相互作用。