新型噻唑烷-4-酮衍生物的设计、合成、表征、抗菌和抗癌研究

IF 1.1 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shumaila Shahid, Mohammad Arshad, Mohd Shoeb Khan, Basim H. Asghar, Mohammad Salim Akhtar, Abdul Karim
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引用次数: 0

摘要

摘要目的微生物感染和癌症是当今最大的健康问题。据报道,新发癌症病例达 1 930 万例,约有 1 000 万人死于癌症。由于嘧啶及其衍生物具有多种化疗作用,研究人员对其进行了大量研究。对新型抗菌和抗癌化疗药物的需求以及嘧啶衍生物的多种药理应用,促使我们对一些新型 3-(取代)-6-(取代)嘧啶-2-基)-2-苯基噻唑烷-4-酮进行了合成和生物学评估。方法:作为寻找新型抗菌剂和抗癌剂研究的一部分,本文重点研究了一些新型 3-(取代)-6-(取代)嘧啶-2-基)-2-苯基噻唑烷-4-酮衍生物的合成。此外,我们还通过傅立叶变换红外光谱(FT-IR)和核磁共振(NMR)对这些化合物的药物相似性进行了虚拟筛选和表征。抗菌和抗癌研究采用了圆盘扩散法、宏观稀释法和 MTT 法。结果与讨论:虚拟筛选结果表明,所有化合物都在活性药物分子的抑制区内。据观察,分析数据有力地支持了目标化合物的结构。在所有合成的化合物中,(IX-XII)、(XIV-XVI) 具有非常好的抗菌效果。其中一些化合物对某些特定病原体具有更好的抗菌潜力。据观察,化合物(XII)是该系列中对几乎所有细菌病原体最有效的化合物。MTT 研究结果表明,化合物 (III)、(IX)、(X) 和 (XII) 的 IC50 值与参考药物多柔比星相似。结论抗菌和抗癌研究结果很有希望,相信对这些化合物的进一步研究和体内分析将有助于生产新型抗菌剂和抗癌剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Design, Synthesis, Characterization, Antimicrobial, Anticancer Studies of Novel Thiazolidin-4-one Derivatives

Design, Synthesis, Characterization, Antimicrobial, Anticancer Studies of Novel Thiazolidin-4-one Derivatives

Design, Synthesis, Characterization, Antimicrobial, Anticancer Studies of Novel Thiazolidin-4-one Derivatives

Objective: Microbial infections and the cancer are the biggest health concerns now days. It has been reported that 19.3 million new cancer cases and approximately 10 million deaths occurred due to cancer. The pyrimidine and their derivatives have been investigated a lot by the researchers due to their versatile chemotherapeutic effects. The unmet demand for the new antimicrobial and anticancer chemotherapeutic agents and the versatile pharmacological applications of pyrimidine derivatives prompted us to perform the synthesis and biological assessment of some novel 3-(substitued)-6-(substituted)pyrimidin-2-yl)-2-phenylthiazolidin-4-one. Methods: As a part of or investigation to find out some novel antimicrobial and anticancer agents, in this paper we focused on the synthesis of some novel 3-(substitued)-6-(substituted)pyrimidin-2-yl)-2-phenylthiazolidin-4-one derivatives. Additionally, the compounds were screened virtually for the drug likeness properties and characterized by FT-IR and NMR. Antimicrobial and anticancer studies were performed using the methods of disc diffusion, macro dilution and MTT assay. Results and Discussion: The virtual screening results revealed that all the compounds were found under the zone of inhibition for an active drug molecule. It was observed that the analytical data strongly supported the structure of the aimed compounds. Among all the synthesized compounds, the compounds (IX–XII), (XIV–XVI) were possessed very good antimicrobial effects. Some of these members represented even better antimicrobial potential against some specific pathogens. The compound (XII) was observed to be the most active compound of the series against almost all bacterial pathogens. The MTT findings revealed that the compounds (III), (IX), (X), (XII) were possessed similar IC50 to the reference drug doxorubicin. Conclusions: The antimicrobial and anticancer findings were promising and it was believed that further studies with these compounds aiming in vivo analysis will be helpful in producing the novel antimicrobial and anticancer agents.

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来源期刊
Russian Journal of Bioorganic Chemistry
Russian Journal of Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
1.80
自引率
10.00%
发文量
118
审稿时长
3 months
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.
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