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Cited 5 time in webofscience Cited 6 time in scopus
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New N-Alkylated Heterocyclic Compounds as Prospective NDM1 Inhibitors: Investigation of In Vitro and In Silico Propertiesopen access

Authors
Kaddouri, YassineBouchal, BtissamAbrigach, FaridEl Kodadi, MohamedBellaoui, MohammedElkamhawy, AhmedTouzani, RachidAbdellattif, Magda H.
Issue Date
Jul-2022
Publisher
MDPI
Keywords
synthesis; pyrazole; antibacterial; antifungal; ADME-Tox; molecular docking
Citation
Pharmaceuticals, v.15, no.7, pp 1 - 19
Pages
19
Indexed
SCIE
SCOPUS
Journal Title
Pharmaceuticals
Volume
15
Number
7
Start Page
1
End Page
19
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/2888
DOI
10.3390/ph15070803
ISSN
1424-8247
1424-8247
Abstract
A new family of pyrazole-based compounds (1-15) was synthesized and characterized using different physicochemical analyses, such as FTIR, UV-Visible, H-1, C-13 NMR, and ESI/LC-MS. The compounds were evaluated for their in vitro antifungal and antibacterial activities against several fungal and bacterial strains. The results indicate that some compounds showed excellent antibacterial activity against E. coli, S. aureus, C. freundii, and L. monocytogenes strains. In contrast, none of the compounds had antifungal activity. Molecular electrostatic potential (MEP) map analyses and inductive and mesomeric effect studies were performed to study the relationship between the chemical structure of our compounds and the biological activity. In addition, molecular docking and virtual screening studies were carried out to rationalize the antibacterial findings to characterize the modes of binding of the most active compounds to the active pockets of NDM1 proteins.
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