Design, Synthesis, Characterization, and Study of in vitro Antioxidant Activity of Some Substituted Biginelli Derivatives

Publish Year: 1402
نوع سند: مقاله ژورنالی
زبان: English
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شناسه ملی سند علمی:

JR_JMCH-6-10_018

تاریخ نمایه سازی: 30 خرداد 1402

Abstract:

The Biginelli class of ۳,۴-dihydropyrimidinone (DHPM) or its thione (DHPMT) derivatives can act as an exciting pharmacophoric moiety, which in turn has attracted the extensive attention of medicinal chemists in the last few decades. Similarly, imidazolidin-۴-one also occupies an inevitable place in drug discovery chemistry. Despite numerous diverse pharmacologic effects ascribed to these two derivatives together being reported, there are few reports on the antioxidant evaluation of the Biginelli class of pyrimidinone derivatives annexed to imidazolidinone by an amide bond. In this study, the synthesis of ۲۰ novel ۳,۴-dihydropyrimidinones with imidazolidin-۴-one derivatives is described. The physical characteristics of the synthesized ۳,۴-DHPM and DHPMT derivatives were determined and analytically characterized by various spectral tools like FT-IR, Lc-Ms/Ms, and proton and carbon NMR. The scavenging radical potential for the synthesized ۲۰ novel Biginelli derivatives was assessed using the DPPH assay. The results indicated that all the tested compounds had good to excellent antioxidant potency in comparison to the standard drug ascorbic acid. The synthesized compounds ۱, ۶, ۸, ۹, ۱۴, ۱۵, ۱۶, ۱۷, ۱۸, and ۱۹ showed a good degree of scavenging potency. Interestingly, remarkable activity was observed with compounds ۱۶, ۱۷, and ۱۹. The present study reveals that not only the compounds with an OH group can exhibit a high degree of scavenging potency, but other groups like -OCH۳, –CH۳, and -Cl can also exhibit activity effectively. In addition, the radical scavenging potential for the studied compounds could be due to either the presence of more than one labile hydrogen atom attached to a nitrogen atom or the conjugated system, i.e. the ۳,۴-dihydropyrimidinone ring attached to an amide linkage, present in these compounds, which would have further sponsored the compound to get stabilized when these compounds become radicals by donating an electron to ROS.

Keywords:

Antioxidant Biginelli derivatives ۳ , ۴-dihydropyrimidinone DPPH Free radicals

Authors

Abdul Lathiff M.K.M

Research scholar, Department of Pharmacy, Faculty of Engineering and Technology, Annamalai University, Chidambaram- ۶۰۸ ۰۰۲, Tamilnadu, India

Suresh Ramalingam

Department of Pharmacy, Faculty of Engineering and Technology, Annamalai University, Chidambaram- ۶۰۸ ۰۰۲, Tamilnadu, India

Senthamarai Rajagopalan

Department of Pharmaceutical Chemistry, Periyar College of Pharmaceutical Sciences, Thiruchirappalli-۶۲۰ ۰۲۱, Tamilnadu, India

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