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新型偕二硫代缩醛化合物的合成及其抗菌、抗真菌、抗惊厥和抗抑郁活性研究。

New Ketene Dithioacetals Generated from 2-Nitroperchlorobutadiene and Investigation of Their Antibacterial, Antifungal, Anticonvulsant and Antidepressant Activities.

机构信息

Istanbul University-Cerrahpasa, Engineering Faculty, Department of Chemistry, Division of Organic Chemistry, 34320, Avcilar, Istanbul, Turkey.

Lviv Polytechnic National University, Department of Technology of Biologically Active Substances, Pharmacy and Biotechnology, 79013, Lviv, Ukraine.

出版信息

Chem Biodivers. 2022 Jul;19(7):e202100931. doi: 10.1002/cbdv.202100931. Epub 2022 Jun 23.

Abstract

The ketene dithioacetal 3 generated from 2-nitroperchlorobutadiene 1 reacted with various heterocyclic amines and aliphatic, aromatic and heterocyclic thiols to produce functionalized new ketene-N,S,S-acetals and S,S,S-acetals 4a-f, 5a-h as heterocyclic dithiolanes. They were separated/purified by chromatographic methods and their exact structure characterization were made clear by spectroscopic methods. These compounds synthesized could act as effective drugs for versatile activity. Evaluation of the antimicrobial effect of the obtained substances determined derivatives 4e and 5h, which have MIC=15.6 μg/mL for the test culture of Mycobacterium luteum bacteria closing to the control drug Vancomycin. The obtained compounds can be proposed as a promising synthetic objects for future molecular design to enhance the antimicrobial action. Ketene dithioacetals 3, 4a, 4b, 4e, 5g (50 mg/kg) exhibited antiseizure effect comparable with reference drug (valproic acid) on the model of pentylenetetrazole-induced convulsions after single oral administration both at 3 h and 24 h. Furthermore, tested dithioacetals possessed prolonged antidepressant activity in forced swim test (FST) considerable decreasing the duration of immobility time compared to reference drug amitriptyline. This is the first study of the investigation of anticonvulsant and antidepressant activities of ketene dithioacetals.

摘要

硝酰氯代丁二烯 1 生成的偕二硫代缩醛 3 与各种杂环胺和脂肪族、芳香族和杂环硫醇反应,生成功能化的新偕二硫代缩醛-N,S,S-和 S,S,S-缩醛 4a-f,5a-h 作为杂环二硫杂环戊烷。它们通过色谱方法分离/纯化,并通过光谱方法明确其确切结构特征。这些合成的化合物可以作为多种活性的有效药物。对所得物质的抗菌效果进行评估,确定了衍生物 4e 和 5h,它们对分枝杆菌的测试培养物的 MIC=15.6μg/mL,接近于对照药物万古霉素。所得化合物可作为未来分子设计的有前途的合成对象,以增强抗菌作用。偕二硫代缩醛 3、4a、4b、4e、5g(50mg/kg)在戊四唑诱导的惊厥模型中,单次口服后 3h 和 24h,与参考药物(丙戊酸)一样,具有抗惊厥作用。此外,与参考药物阿米替林相比,测试的二硫代缩醛在强迫游泳试验(FST)中具有延长的抗抑郁作用,显著降低了不动时间的持续时间。这是对偕二硫代缩醛的抗惊厥和抗抑郁活性进行研究的首次研究。

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