Design, Docking, Characterisation, and Synthesis of Pyrimidine Derivatives for Antidepressant Activity.

Ashwini Jadhav, Sunil G Shingade, Prachita G Dessai, Bheemanagouda S Biradar, Shivalingrao MamleDesai
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Abstract

Background: According to the report, in 2022, the prevalence rate of depression in India was 4.50%, and the cases stood at 56,675,969. The development of antidepressant agents has reduced the number of depressant and suicidal cases. Many researchers have found that pyrimidine possesses antidepressant activity. With this background, we thought of synthesizing pyrimidine derivatives.

Objective: The objective of this study is to carry out molecular docking, synthesis, characterization, and evaluation of 2-((4,6-diphenylpyrimidin-2-yl)oxy)-N-phenylacetamide derivatives (17-26) as in vivo antidepressant agent.

Method: The designed compounds were checked for their activity using Molegro virtual docker (MVD) and were further synthesized. Benzaldehyde reacted with acetophenone to give compound (3), which gave compound (4) upon reaction with urea. In another reaction, substituted anilines (5) were reacted with chloroacetyl chloride (6) to yield compounds (7-16), which upon further reaction with compound (4) yielded the final derivatives (17-26). The synthesized compounds were characterized by spectral analysis and checked for their antidepressant activity.

Result: The MolDock scores of the derivatives ranged from -147.097 to -182.095, whereas of active ligand IXX_801 was -115.566. All the synthesized pyrimidine derivatives showed better affinity towards the Cryo-EM structure of the wild-type human serotonin transporter complexed with vilazodone, imipramine, and 15B8 Fab protein (PDB ID: 7LWD) as compared to standard drug clomipramine (-101.064). All the synthesized derivatives were screened for antidepressant activity at a 100mg/kg dose level compared to the standard clomipramine HCl at a dose level of 20mg/kg. Among all the synthesized derivatives, compound 24 showed the most potent antidepressant activity, and Compound 20 showed moderate antidepressant activity, which reduced the duration of immobility times to 35.42% and 31.97% at 100mg/kg dose level when compared to the control, respectively.

Conclusion: Compound 24 showed the highest MolDock score as well as found to be the most potent antidepressant agent.

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具有抗抑郁活性的嘧啶衍生物的设计、对接、表征和合成。
背景:根据该报告,2022年,印度抑郁症的患病率为4.50%,病例数为56675969例。抗抑郁药的开发减少了抑郁症和自杀病例的数量。许多研究人员发现嘧啶具有抗抑郁活性。在这种背景下,我们想到了合成嘧啶衍生物。目的:对2-(4,6-二苯基嘧啶-2-基)氧基)-N-苯乙酰胺衍生物(17-26)进行分子对接、合成、表征和评价。方法:使用Molegro虚拟docker(MVD)检测设计的化合物的活性,并进一步合成。苯甲醛与苯乙酮反应得到化合物(3),在与尿素反应时得到化合物(4)。在另一个反应中,取代苯胺(5)与氯乙酰氯(6)反应得到化合物(7-16),在与化合物(4)进一步反应时得到最终衍生物(17-26)。通过光谱分析对合成的化合物进行了表征,并检查了它们的抗抑郁活性。结果:这些衍生物的MolDock评分在-147.097至-182.095之间,而活性配体IXX_801的MolDock评分为-115.566。所有合成的嘧啶衍生物都显示出对与维拉唑酮、丙咪嗪、异丙肾上腺素和异丙肾上腺素复合的野生型人5-羟色胺转运蛋白的Cryo-EM结构的更好的亲和力,和15B8 Fab蛋白(PDB ID:7LWD)。与标准药物克罗米帕明(-101.064)相比,所有合成的衍生物在100mg/kg剂量水平下均筛选出抗抑郁活性,与20mg/kg剂量水平的标准盐酸克罗米帕胺相比。在所有合成的衍生物中,化合物24表现出最有效的抗抑郁活性,化合物20表现出中等的抗抑郁活动,与对照相比,在100mg/kg剂量水平下,其静止时间分别减少到35.42%和31.97%。结论:化合物24表现出最高的MolDock评分,并且被发现是最有效的抗抑郁剂。
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