Synthesis and Spectral Identification of Three Schiff Bases with a 2-(Piperazin-1-yl)- N -(thiophen-2-yl methylene)ethanamine Moiety Acting as Novel Pancreatic Lipase Inhibitors: Thermal, DFT, Antioxidant, Antibacterial, and Molecular Docking Investigations

Three new tetradentate NNNS Schiff bases ( - ) derived from 2-(piperidin-4-yl)ethanamine were prepared in high yields. UV-Visible and FTIR spectroscopy were used to monitor the dehydration reaction between 2-(piperidin-4-yl)ethanamine and the corresponding aldehydes. Structures of the derived Schiff...

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Published inMolecules (Basel, Switzerland) Vol. 25; no. 9; p. 2253
Main Authors Warad, Ismail, Ali, Oraib, Al Ali, Anas, Jaradat, Nidal Amin, Hussein, Fatima, Abdallah, Lubna, Al-Zaqri, Nabil, Alsalme, Ali, Alharthi, Fahad A
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 11.05.2020
MDPI
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Summary:Three new tetradentate NNNS Schiff bases ( - ) derived from 2-(piperidin-4-yl)ethanamine were prepared in high yields. UV-Visible and FTIR spectroscopy were used to monitor the dehydration reaction between 2-(piperidin-4-yl)ethanamine and the corresponding aldehydes. Structures of the derived Schiff bases were deduced by H and C NMR, FTIR, UV-Vis, MS, EA, EDS, and TG-derived physical measurements. DFT/B3LYP theoretical calculations for optimization, TD-DFT, frequency, Molecular Electrostatic Potential (MEP), and highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) / were performed for . The in vitro antimicrobial activities of the three Schiff bases were evaluated against several types of bacteria by disk diffusion test using Gentamicin as the standard antibiotic. Schiff bases revealed good antioxidant activity by the DPPH method, and the IC values were compared to the Trolox standard. Pancreatic porcine lipase inhibition assay of the synthesized compounds revealed promising activity as compared to the Orlistat reference.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules25092253