Prospects for the creation of new drug candidates with antidepressant activity among thietanes

Q4 Medicine Kazanskij Medicinskij Zurnal Pub Date : 2023-09-28 DOI:10.17816/kmj346694
Irina L. Nikitina, Gulnara G. Gaisina, Elena E. Klen, Galina A. Rozit, Alexander V. Samorodov
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Abstract

The article presents the results of systematic studies on the search for new biologically active molecules with antidepressant activity in the series of thietane-containing heterocyclic compounds and 3-substituted thietane dioxides. The used strategy for the search for antidepressant substances, based on in vivo pharmacological screening in combination with in silico methods of mathematical modeling and toxico-pharmacokinetic evaluation, is described. Studies of the biological activity of thietane-containing reaction products of azoles with thiiranes have been carried out in the series of thietanylimidazoles, titanixanthines, thietanyltriazoles, thietanyltriazolones, and 3-substituted thietane-1,1-dioxides (more than 300 compounds have been studied). The main results of the preclinical evaluation of promising drug candidates with antidepressant activity, 3-methoxythiethane-1,1-dioxide and 3-ethoxythiethane-1,1-dioxide, are presented. Both 3-substituted thietane-1,1-dioxides are characterized by low toxicity when administered intraperitoneally to mice (class IV low toxicity), the absence of toxic risks (mutagenic, carcinogenic, reproductive toxicity, local irritant action), high pharmaceutical potential (compliance with the rule of five Lipinsky), a wide range of action and pronounced antidepressant activity, not inferior to the reference drug amitriptyline (10 mg/kg), confirmed in highly valid in vivo models of depressive-like states (chronic mild stress and resident intruder). In tests of neuropharmacological interaction, it was found that the proposed mechanism of action of 3-substituted thietane-1,1-dioxides is associated with stimulation of 5-HT1A receptors, blockade of 5-HT2A/2C receptors and/or 2-adrenergic receptors. The need for further research is substantiated in order to create domestic first in class antidepressants on their basis.
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开发具有抗抑郁活性的新型候选药物的前景
本文介绍了在含硫烷杂环化合物和3-取代硫烷二氧化物系列中寻找具有抗抑郁活性的新型生物活性分子的系统研究结果。用于寻找抗抑郁药物的策略,基于体内药理学筛选结合计算机方法的数学建模和毒性药代动力学评价,被描述。对含噻烷的唑类与噻烷类反应产物的生物活性进行了研究,研究对象包括:二乙胺基咪唑类、钛黄嘌呤类、二乙胺基三唑类、三乙胺基三唑类和3-取代噻烷-1,1-二氧化物等(研究了300多种化合物)。本文介绍了具有抗抑郁活性的候选药物3-甲氧基乙烷-1,1-二氧化二氮和3-乙氧基乙烷-1,1-二氧化二氮的临床前评价的主要结果。这两种3-取代噻吩-1,1-二氧化物的特点是:小鼠腹腔注射时毒性低(IV类低毒),没有毒性风险(致突变、致癌、生殖毒性、局部刺激作用),具有很高的药物潜力(符合五利平斯基规则),作用范围广,抗抑郁活性明显,不逊于参比药物阿米替林(10 mg/kg)。在高度有效的体内抑郁样状态模型(慢性轻度应激和常驻入侵者)中得到证实。在神经药理相互作用试验中,发现3-取代硫烷-1,1-二氧化物的作用机制与刺激5-HT1A受体、阻断5-HT2A/2C受体和/或2-肾上腺素能受体有关。为了在此基础上创造国内一流的抗抑郁药,需要进一步的研究。
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来源期刊
Kazanskij Medicinskij Zurnal
Kazanskij Medicinskij Zurnal Medicine-General Medicine
CiteScore
0.40
自引率
0.00%
发文量
553
审稿时长
18 weeks
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