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Inhibition of SARS-CoV 3CL protease by flavonoids

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.145-151

2020

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Virtual screening, molecular dynamics and structure-activity relationship studies to identify potent approved drugs for Covid-19 treatment

Journal of biomolecular structure & dynamics, 2021-11, Vol.39 (16), p.6231-6241

2021

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Design, synthesis and evaluation of carbazole derivatives as potential antimicrobial agents

Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.296-307

2021

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Matrix metalloproteinases (MMPs), the main extracellular matrix (ECM) enzymes in collagen degradation, as a target for anticancer drugs

Journal of enzyme inhibition and medicinal chemistry, 2016-11, Vol.31 (sup1), p.177-183

2016

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Discovery of new 6-ureido/amidocoumarins as highly potent and selective inhibitors for the tumour-relevant carbonic anhydrases IX and XII

Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.2154603-2154603

2023

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Design, synthesis, and evaluation of cyclic C7-bridged monocarbonyl curcumin analogs containing an o -methoxy phenyl group as potential agents against gastric cancer

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2314233-2314233

2024

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Design, synthesis, molecular modelling and biological evaluation of novel 3-(2-naphthyl)-1-phenyl-1H-pyrazole derivatives as potent antioxidants and 15-Lipoxygenase inhibitors

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.847-863

2020

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Novel tetrahydronaphthalen-1-yl-phenethyl ureas: synthesis and dual antibacterial-anticancer activities

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2286925-2286925

2024

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Application of triazoles in the structural modification of natural products

Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.1115-1144

2021

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Discovery of novel potent drugs for influenza by inhibiting the vital function of neuraminidase via fragment-based drug design (FBDD) and molecular dynamics simulation strategies

Journal of biomolecular structure & dynamics, 2024-12, Vol.42 (18), p.9294-9308

2024

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Design, synthesis, and antiprotozoal evaluation of new 2,4-bis[(substituted-aminomethyl)phenyl]quinoline, 1,3-bis[(substituted-aminomethyl)phenyl]isoquinoline and 2,4-bis[(substituted-aminomethyl)phenyl]quinazoline derivatives

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.432-459

2020

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Design, synthesis and in vitro biological studies of novel triazoles with potent and broad-spectrum antifungal activity

Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.2244696-2244696

2023

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Interaction of flavonols with human serum albumin: a biophysical study showing structure-activity relationship and enhancement when coated on silver nanoparticles

Journal of biomolecular structure & dynamics, 2019-04, Vol.37 (6), p.1414-1426

2019

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Flavonoids as inhibitors of human neutrophil elastase

Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.1016-1028

2021

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Benzothiazole derivatives as anticancer agents

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.265-279

2020

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Synthesis, characterisation, biological evaluation and in silico studies of sulphonamide Schiff bases

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.950-962

2020

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Investigating the binding affinity, interaction, and structure-activity-relationship of 76 prescription antiviral drugs targeting RdRp and Mpro of SARS-CoV-2

Journal of biomolecular structure & dynamics, 2021-11, Vol.39 (16), p.6290-6305

2021

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Discovery of new 1,4-disubstituted 1,2,3-triazoles: in silico ADME profiling, molecular docking and biological evaluation studies

Journal of biomolecular structure & dynamics, 2023-03, Vol.41 (5), p.1988-2001

2023

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Chemical constituents of Hericium erinaceum associated with the inhibitory activity against cellular senescence in human umbilical vascular endothelial cells

Journal of enzyme inhibition and medicinal chemistry, 2015-11, Vol.30 (6), p.934-940

2015

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Isatin thiazoline hybrids as dual inhibitors of HIV-1 reverse transcriptase

Journal of enzyme inhibition and medicinal chemistry, 2017-01, Vol.32 (1), p.130-136

2017

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Paving the way towards effective plant-based inhibitors of hyaluronidase and tyrosinase: a critical review on a structure-activity relationship

Journal of enzyme inhibition and medicinal chemistry, 2022-12, Vol.37 (1), p.1120-1195

2022

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Design, synthesis, and biological investigation of selective human carbonic anhydrase II, IX, and XII inhibitors using 7-aryl/heteroaryl triazolopyrimidines bearing a sulfanilamide scaffold

Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.2270180-2270180

2023

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A review on synthetic chalcone derivatives as tubulin polymerisation inhibitors

Journal of enzyme inhibition and medicinal chemistry, 2022-12, Vol.37 (1), p.9-38

2022

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Synthesis of 4,5-disubstituted-2-thioxo-1,2,3,4-tetrahydropyrimidines and investigation of their acetylcholinesterase, butyrylcholinesterase, carbonic anhydrase I/II inhibitory and antioxidant activities

Journal of enzyme inhibition and medicinal chemistry, 2016-11, Vol.31 (sup3), p.1-9

2016

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Small molecule compounds with good anti-inflammatory activity reported in the literature from 01/2009 to 05/2021: a review

Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.2139-2159

2021

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Inhibition of SARS-CoV 3CL protease by flavonoids

Virtual screening, molecular dynamics and structure-activity relationship studies to identify potent approved drugs for Covid-19 treatment

Design, synthesis and evaluation of carbazole derivatives as potential antimicrobial agents

Matrix metalloproteinases (MMPs), the main extracellular matrix (ECM) enzymes in collagen degradation, as a target for anticancer drugs

Discovery of new 6-ureido/amidocoumarins as highly potent and selective inhibitors for the tumour-relevant carbonic anhydrases IX and XII

Design, synthesis, and evaluation of cyclic C7-bridged monocarbonyl curcumin analogs containing an o -methoxy phenyl group as potential agents against gastric cancer

Design, synthesis, molecular modelling and biological evaluation of novel 3-(2-naphthyl)-1-phenyl-1H-pyrazole derivatives as potent antioxidants and 15-Lipoxygenase inhibitors

Novel tetrahydronaphthalen-1-yl-phenethyl ureas: synthesis and dual antibacterial-anticancer activities

Application of triazoles in the structural modification of natural products

Discovery of novel potent drugs for influenza by inhibiting the vital function of neuraminidase via fragment-based drug design (FBDD) and molecular dynamics simulation strategies

Design, synthesis, and antiprotozoal evaluation of new 2,4-bis[(substituted-aminomethyl)phenyl]quinoline, 1,3-bis[(substituted-aminomethyl)phenyl]isoquinoline and 2,4-bis[(substituted-aminomethyl)phenyl]quinazoline derivatives

Design, synthesis and in vitro biological studies of novel triazoles with potent and broad-spectrum antifungal activity

Interaction of flavonols with human serum albumin: a biophysical study showing structure-activity relationship and enhancement when coated on silver nanoparticles

Flavonoids as inhibitors of human neutrophil elastase

Benzothiazole derivatives as anticancer agents

Synthesis, characterisation, biological evaluation and in silico studies of sulphonamide Schiff bases

Investigating the binding affinity, interaction, and structure-activity-relationship of 76 prescription antiviral drugs targeting RdRp and Mpro of SARS-CoV-2

Discovery of new 1,4-disubstituted 1,2,3-triazoles: in silico ADME profiling, molecular docking and biological evaluation studies

Chemical constituents of Hericium erinaceum associated with the inhibitory activity against cellular senescence in human umbilical vascular endothelial cells

Isatin thiazoline hybrids as dual inhibitors of HIV-1 reverse transcriptase

Paving the way towards effective plant-based inhibitors of hyaluronidase and tyrosinase: a critical review on a structure-activity relationship

Design, synthesis, and biological investigation of selective human carbonic anhydrase II, IX, and XII inhibitors using 7-aryl/heteroaryl triazolopyrimidines bearing a sulfanilamide scaffold

A review on synthetic chalcone derivatives as tubulin polymerisation inhibitors

Synthesis of 4,5-disubstituted-2-thioxo-1,2,3,4-tetrahydropyrimidines and investigation of their acetylcholinesterase, butyrylcholinesterase, carbonic anhydrase I/II inhibitory and antioxidant activities

Small molecule compounds with good anti-inflammatory activity reported in the literature from 01/2009 to 05/2021: a review

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