Molecular docking, derivatization, characterization and biological assays of amantadine

<b>Background:</b> Derivatization has been tremendously utilized in the field of drug discovery for optimizing the pharmacological properties and improving safety, efficacy and selectivity.<b>Methodology:</b> Schiff's bases (AD1-AD11) are synthesized through amantadine condensation with different aldehydes and ketones. Fourier transform infrared, <sup>1</sup>H NMR, <sup>13</sup>C NMR, TLC, liquid chromatography mass spectrometry analysis, <i>in silico</i> studies, molecular docking and antiviral activity through hemagglutinin test were performed for evaluation of new compounds.<b>Results:</b> AD2, 3 and 9-11 showed greater antiviral activity than the parent drug. Among all derivatives, AD2 and AD3 exhibited good potential against α-amylase while AD7 and AD10 showed stronger inhibition against α-glucosidase.<b>Conclusion:</b> So, it is concluded that the most potent derivatives can be used as lead compounds in novel drug design of antiviral antidiabetic agents.

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Publication Details

Journal
Future Medicinal Chemistry
Published
2024-08-09
DOI
https://doi.org/10.1080/17568919.2024.2385294
Citations
3
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.75
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article

Molecular docking, derivatization, characterization and biological assays of amantadine

Breena Awan, Farhat Ullah, Mohsin Abbas Khan, Muhammad Toseef Akram et al.
3 citations
Future Medicinal Chemistry
Synthesis and biological activity
0.75
article

Molecular docking, derivatization, characterization and biological assays of amantadine

Breena Awan, Farhat Ullah, Mohsin Abbas Khan, Muhammad Toseef Akram, Irshad Ahmad, Muhammad Rizwan Khan, Zarmeena Yasmeen
article en
3 citations

Abstract

<b>Background:</b> Derivatization has been tremendously utilized in the field of drug discovery for optimizing the pharmacological properties and improving safety, efficacy and selectivity.<b>Methodology:</b> Schiff's bases (AD1-AD11) are synthesized through amantadine condensation with different aldehydes and ketones. Fourier transform infrared, <sup>1</sup>H NMR, <sup>13</sup>C NMR, TLC, liquid chromatography mass spectrometry analysis, <i>in silico</i> studies, molecular docking and antiviral activity through hemagglutinin test were performed for evaluation of new compounds.<b>Results:</b> AD2, 3 and 9-11 showed greater antiviral activity than the parent drug. Among all derivatives, AD2 and AD3 exhibited good potential against α-amylase while AD7 and AD10 showed stronger inhibition against α-glucosidase.<b>Conclusion:</b> So, it is concluded that the most potent derivatives can be used as lead compounds in novel drug design of antiviral antidiabetic agents.

Future Medicinal ChemistryVol. 16(18)
Islamia University of Bahawalpur (PK)
Openalex Percentile: Top 33%
Synthesis and biological activity
0.75
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