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

被引:0
|
作者
Shahid, Shumaila [1 ,3 ]
Arshad, Mohammad [2 ]
Khan, Mohd Shoeb [2 ]
Asghar, Basim H. [4 ]
Akhtar, Mohammad Salim [5 ]
Karim, Abdul [6 ]
机构
[1] ICAR Indian Agr Res Inst, Div Plant Pathol, New Delhi 110012, India
[2] Al Fayha Coll, Fac Engn & Technol, Dept Gen Studies & Sci, Jubail Ind City 31961, Saudi Arabia
[3] Jamia Millia Islamia, Fac Engn & Technol, Dept Appl Sci & Humanities, New Delhi 110025, India
[4] Umm Al Qura Univ, Fac Sci Appl, Dept Chem, Mecca, Saudi Arabia
[5] Univ Bahrain, Coll Sci, Dept Chem, Manama 32038, Bahrain
[6] Jamia Millia Islamia, Mat Res Lab, Dept Chem, Fac Nat Sci, New Delhi 110025, India
关键词
synthesis; characterization; thiazolidin-4-one; antimicrobial; anticancer; DOCKING; ASSAY;
D O I
10.1134/S1068162024040332
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1535 / 1550
页数:16
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