{"title":"不同的五元杂环衍生物的合成、表征及其作为抗氧化剂和体外抗菌剂的效果评估","authors":"Asmaa A. Maryoosh, Oday H. R. Al-Jeilawi","doi":"10.1134/S1068162024040265","DOIUrl":null,"url":null,"abstract":"<p><b>Objective:</b> This study involved synthesis of a new series of different five-membered heterocyclic derivatives, testing their antioxidant activity, and examining their potential <i>in vitro</i> antimicrobial agents. <b>Methods:</b> The synthesis of the derivatives involved a three-step process. Initially, succinyl chloride was reacted with methanol, followed by a reaction with 80% hydrazine hydrate through a nucleophilic addition-elimination mechanism, resulting in the formation of succinohydrazide (<b>I</b>). This compound was then employed as a precursor for the synthesis of Schiff bases (<b>II</b>), and (<b>III</b>) by reacting it with <i>m</i>-nitro benzaldehyde and <i>p</i>-nitro benzaldehyde. Following this, a ring closure reaction was applied using thioglycolic acid, glycolic acid, and glycine, resulting in the synthesis of different five-membered heterocyclic rings (<b>IV</b>–<b>IX</b>). <b>Results and Discussion:</b> The formation of the prepared derivatives was confirmed by FT-IR, <sup>1</sup>H NMR, and <sup>13</sup>C NMR spectroscopy. Comparative analysis with L-ascorbic acid as a standard revealed that all the prepared compounds exhibited excellent antioxidant activities. In terms of antimicrobial activity, the tested derivatives showed moderate activity against both positive and negative types of bacteria, when compared to the reference drug Ciprofloxacin. Additionally, the antifungal test showed moderate activity for all the tested compounds against a specific pathogenic fungus, with Clotrimazole being as the reference drug. The antimicrobial activity of the synthesized compounds was found to be dependent on the type of heterocyclic rings containing S, O, and N atoms. These atoms were observed to enhance antimicrobial activity by donating electrons and becoming active. Additionally, the presence of active functional groups such as C=O, NO<sub>2</sub>, and C=N contributed to this observed result. <b>Conclusions:</b> All of the synthesized compounds have demonstrated excellent antioxidant agents. Most of them have shown promising antimicrobial activity against certain bacteria strains, and effectiveness against a pathogenic fungus.</p>","PeriodicalId":758,"journal":{"name":"Russian Journal of Bioorganic Chemistry","volume":"50 4","pages":"1551 - 1562"},"PeriodicalIF":1.1000,"publicationDate":"2024-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis, Characterization of Different Five-Membered Heterocyclic Derivatives, Evaluated Their as Antioxidant, and In Vitro Antimicrobial Agents\",\"authors\":\"Asmaa A. Maryoosh, Oday H. R. Al-Jeilawi\",\"doi\":\"10.1134/S1068162024040265\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><b>Objective:</b> This study involved synthesis of a new series of different five-membered heterocyclic derivatives, testing their antioxidant activity, and examining their potential <i>in vitro</i> antimicrobial agents. <b>Methods:</b> The synthesis of the derivatives involved a three-step process. Initially, succinyl chloride was reacted with methanol, followed by a reaction with 80% hydrazine hydrate through a nucleophilic addition-elimination mechanism, resulting in the formation of succinohydrazide (<b>I</b>). This compound was then employed as a precursor for the synthesis of Schiff bases (<b>II</b>), and (<b>III</b>) by reacting it with <i>m</i>-nitro benzaldehyde and <i>p</i>-nitro benzaldehyde. Following this, a ring closure reaction was applied using thioglycolic acid, glycolic acid, and glycine, resulting in the synthesis of different five-membered heterocyclic rings (<b>IV</b>–<b>IX</b>). <b>Results and Discussion:</b> The formation of the prepared derivatives was confirmed by FT-IR, <sup>1</sup>H NMR, and <sup>13</sup>C NMR spectroscopy. Comparative analysis with L-ascorbic acid as a standard revealed that all the prepared compounds exhibited excellent antioxidant activities. In terms of antimicrobial activity, the tested derivatives showed moderate activity against both positive and negative types of bacteria, when compared to the reference drug Ciprofloxacin. Additionally, the antifungal test showed moderate activity for all the tested compounds against a specific pathogenic fungus, with Clotrimazole being as the reference drug. The antimicrobial activity of the synthesized compounds was found to be dependent on the type of heterocyclic rings containing S, O, and N atoms. These atoms were observed to enhance antimicrobial activity by donating electrons and becoming active. Additionally, the presence of active functional groups such as C=O, NO<sub>2</sub>, and C=N contributed to this observed result. <b>Conclusions:</b> All of the synthesized compounds have demonstrated excellent antioxidant agents. Most of them have shown promising antimicrobial activity against certain bacteria strains, and effectiveness against a pathogenic fungus.</p>\",\"PeriodicalId\":758,\"journal\":{\"name\":\"Russian Journal of Bioorganic Chemistry\",\"volume\":\"50 4\",\"pages\":\"1551 - 1562\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2024-08-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Journal of Bioorganic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S1068162024040265\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Bioorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1068162024040265","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
摘要目的:本研究涉及合成一系列新的不同五元杂环衍生物,测试它们的抗氧化活性,并研究它们潜在的体外抗菌剂。方法:衍生物的合成分为三个步骤。首先,琥珀酰氯与甲醇反应,然后通过亲核加成-消除机制与 80% 的水合肼反应,生成琥珀酰肼 (I)。然后,该化合物被用作合成希夫碱 (II) 和 (III) 的前体,与间硝基苯甲醛和对硝基苯甲醛发生反应。随后,利用硫代乙醇酸、乙醇酸和甘氨酸进行闭环反应,合成了不同的五元杂环(IV-IX)。结果与讨论:傅立叶变换红外光谱、1H NMR 和 13C NMR 光谱证实了所制备衍生物的形成。以左旋抗坏血酸为标准进行的比较分析表明,所有制备的化合物都具有出色的抗氧化活性。在抗菌活性方面,与参考药物环丙沙星相比,受试衍生物对阳性和阴性细菌均表现出中等程度的活性。此外,在抗真菌测试中,以克霉唑为参照药物,所有测试化合物对一种特定致病真菌都显示出中等程度的活性。研究发现,合成化合物的抗菌活性取决于含有 S、O 和 N 原子的杂环类型。据观察,这些原子通过提供电子而变得活跃,从而增强了抗菌活性。此外,C=O、NO2 和 C=N 等活性官能团的存在也促成了这一结果。结论所有合成的化合物都具有出色的抗氧化性。它们中的大多数对某些细菌菌株具有良好的抗菌活性,并对一种致病真菌有效。
Synthesis, Characterization of Different Five-Membered Heterocyclic Derivatives, Evaluated Their as Antioxidant, and In Vitro Antimicrobial Agents
Objective: This study involved synthesis of a new series of different five-membered heterocyclic derivatives, testing their antioxidant activity, and examining their potential in vitro antimicrobial agents. Methods: The synthesis of the derivatives involved a three-step process. Initially, succinyl chloride was reacted with methanol, followed by a reaction with 80% hydrazine hydrate through a nucleophilic addition-elimination mechanism, resulting in the formation of succinohydrazide (I). This compound was then employed as a precursor for the synthesis of Schiff bases (II), and (III) by reacting it with m-nitro benzaldehyde and p-nitro benzaldehyde. Following this, a ring closure reaction was applied using thioglycolic acid, glycolic acid, and glycine, resulting in the synthesis of different five-membered heterocyclic rings (IV–IX). Results and Discussion: The formation of the prepared derivatives was confirmed by FT-IR, 1H NMR, and 13C NMR spectroscopy. Comparative analysis with L-ascorbic acid as a standard revealed that all the prepared compounds exhibited excellent antioxidant activities. In terms of antimicrobial activity, the tested derivatives showed moderate activity against both positive and negative types of bacteria, when compared to the reference drug Ciprofloxacin. Additionally, the antifungal test showed moderate activity for all the tested compounds against a specific pathogenic fungus, with Clotrimazole being as the reference drug. The antimicrobial activity of the synthesized compounds was found to be dependent on the type of heterocyclic rings containing S, O, and N atoms. These atoms were observed to enhance antimicrobial activity by donating electrons and becoming active. Additionally, the presence of active functional groups such as C=O, NO2, and C=N contributed to this observed result. Conclusions: All of the synthesized compounds have demonstrated excellent antioxidant agents. Most of them have shown promising antimicrobial activity against certain bacteria strains, and effectiveness against a pathogenic fungus.
期刊介绍:
Russian Journal of Bioorganic Chemistry publishes reviews and original experimental and theoretical studies on the structure, function, structure–activity relationships, and synthesis of biopolymers, such as proteins, nucleic acids, polysaccharides, mixed biopolymers, and their complexes, and low-molecular-weight biologically active compounds (peptides, sugars, lipids, antibiotics, etc.). The journal also covers selected aspects of neuro- and immunochemistry, biotechnology, and ecology.