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Synthesis, molecular docking study and biological evaluation of new pyrrole scaffolds as potential antitubercular agents for dual targeting of enoyl ACP reductase and dihydrofolate reductase

PloS one, 2024-05, Vol.19 (5), p.e0303173-e0303173

2024

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Multi-spectroscopic investigation of the binding interaction of fosfomycin with bovine serum albumin

Journal of pharmaceutical analysis, 2015-08, Vol.5 (4), p.249-255

2015

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New Urea Derivatives as Potential Antimicrobial Agents: Synthesis, Biological Evaluation, and Molecular Docking Studies

Antibiotics (Basel), 2019-10, Vol.8 (4), p.178

2019

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Synthesis of novel indole, 1,2,4-triazole derivatives as potential glucosidase inhibitors

Journal of King Saud University. Science, 2020-12, Vol.32 (8), p.3388-3399

2020

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Functionalization of 3-chloroformylcoumarin to coumarin Schiff bases using reusable catalyst: an approach to molecular docking and biological studies

Royal Society open science, 2018-05, Vol.5 (5), p.172416-172416

2018

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Synthesis, Molecular Docking Study, and Biological Evaluation of New 4-(2,5-Dimethyl-1 H -pyrrol-1-yl)- N '-(2-(substituted)acetyl)benzohydrazides as Dual Enoyl ACP Reductase and DHFR Enzyme Inhibitors

Antibiotics (Basel), 2023-04, Vol.12 (4), p.763

2023

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Enoyl ACP reductase as effective target for the synthesized novel antitubercular drugs: a-state-of-the-art

Mini reviews in medicinal chemistry, 2014-01, Vol.14 (8), p.678

2014

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Synthesis, characterization and molecular docking studies of substituted 4-coumarinylpyrano[2,3-c]pyrazole derivatives as potent antibacterial and anti-inflammatory agents

European journal of medicinal chemistry, 2017-01, Vol.125, p.101-116

2017

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Synthesis of coumarin-thioether conjugates as potential anti-tubercular agents: Their molecular docking and X-ray crystal studies

Journal of molecular structure, 2022-10, Vol.1266, p.133452, Article 133452

2022

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One pot Click chemistry: A three component reaction for the synthesis of 2-mercaptobenzimidazole linked coumarinyl triazoles as anti-tubercular agents

Bioorganic & medicinal chemistry letters, 2016-10, Vol.26 (19), p.4709-4713

2016

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Synthesis of coumarin-theophylline hybrids as a new class of anti-tubercular and anti-microbial agents

European journal of medicinal chemistry, 2018-02, Vol.146, p.747-756

2018

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Synthesis, antimycobacterial screening and ligand-based molecular docking studies on novel pyrrole derivatives bearing pyrazoline, isoxazole and phenyl thiourea moieties

European journal of medicinal chemistry, 2016-01, Vol.107, p.133-152

2016

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Synthesis of novel 5-(2,5-bis(2,2,2-trifluoroethoxy)phenyl)-1,3,4-oxadiazole-2-thiol derivatives as potential glucosidase inhibitors

Bioorganic chemistry, 2021-09, Vol.114, p.105046-105046, Article 105046

2021

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Spectral and molecular modelling studies of sulfadoxine interaction with bovine serum albumin

Journal of photochemistry and photobiology. A, Chemistry., 2019-09, Vol.382, p.111871, Article 111871

2019

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Interaction of Hydralazine with Human Serum Albumin and Effect of β‑Cyclodextrin on Binding: Insights from Spectroscopic and Molecular Docking Techniques

Industrial & engineering chemistry research, 2016-05, Vol.55 (19), p.5454-5464

2016

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Synthesis, molecular modeling and BACE-1 inhibitory study of tetrahydrobenzo[b] pyran derivatives

Bioorganic chemistry, 2019-03, Vol.84, p.202-210

2019

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Novel quinoxalinyl chalcone hybrid scaffolds as enoyl ACP reductase inhibitors: Synthesis, molecular docking and biological evaluation

Bioorganic & medicinal chemistry letters, 2017-05, Vol.27 (10), p.2174-2180

2017

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Synthesis, characterization and antitubercular activities of novel pyrrolyl hydrazones and their Cu-complexes

European journal of medicinal chemistry, 2016-10, Vol.121, p.21-39

2016

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Design, docking analysis, identification, and synthesis of novel 3-(((substituted phenyl) amino)methyl)-2-methylquinazolin-4(3H)-one compounds to fight tuberculosis

Drug Discoveries & Therapeutics, 2016, Vol.10(4), pp.188-194

2016

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Microwave assisted regioselective synthesis of quinoline appended triazoles as potent anti-tubercular and antifungal agents via copper (I) catalyzed cycloaddition

Bioorganic & medicinal chemistry letters, 2021-06, Vol.41, p.127984, Article 127984

2021

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A click chemistry approach for the synthesis of mono and bis aryloxy linked coumarinyl triazoles as anti-tubercular agents

European journal of medicinal chemistry, 2015-11, Vol.105, p.194-207

2015

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Green synthesis of therapeutically active 1,3,4-oxadiazoles as antioxidants, selective COX-2 inhibitors and their in silico studies

Bioorganic & medicinal chemistry letters, 2021-07, Vol.43, p.128112-128112, Article 128112

2021

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WELPSA: A natural catalyst of alkali and alkaline earth metals for the facile synthesis of tetrahydrobenzo[b]pyrans and pyrano[2,3‐d]pyrimidinones as inhibitors of SARS‐CoV‐2

Applied organometallic chemistry, 2022-01, Vol.36 (1), p.e6469-n/a

2022

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New thiophene-1,3,4-oxadiazole-thiazolidine-2,4-dione hybrids: Synthesis, MCF-7 inhibition and binding studies

Bioorganic chemistry, 2024-02, Vol.143, p.107003-107003, Article 107003

2024

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Fluorenone-thiazolidine-4-one scaffolds as antidiabetic and antioxidant agents: design, synthesis, X-ray crystal structures, and binding and computational studies

New journal of chemistry, 2023-07, Vol.47 (28), p.13581-13599

2023

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Synthesis, molecular docking study and biological evaluation of new pyrrole scaffolds as potential antitubercular agents for dual targeting of enoyl ACP reductase and dihydrofolate reductase

Multi-spectroscopic investigation of the binding interaction of fosfomycin with bovine serum albumin

New Urea Derivatives as Potential Antimicrobial Agents: Synthesis, Biological Evaluation, and Molecular Docking Studies

Synthesis of novel indole, 1,2,4-triazole derivatives as potential glucosidase inhibitors

Functionalization of 3-chloroformylcoumarin to coumarin Schiff bases using reusable catalyst: an approach to molecular docking and biological studies

Synthesis, Molecular Docking Study, and Biological Evaluation of New 4-(2,5-Dimethyl-1 H -pyrrol-1-yl)- N '-(2-(substituted)acetyl)benzohydrazides as Dual Enoyl ACP Reductase and DHFR Enzyme Inhibitors

Enoyl ACP reductase as effective target for the synthesized novel antitubercular drugs: a-state-of-the-art

Synthesis, characterization and molecular docking studies of substituted 4-coumarinylpyrano[2,3-c]pyrazole derivatives as potent antibacterial and anti-inflammatory agents

Synthesis of coumarin-thioether conjugates as potential anti-tubercular agents: Their molecular docking and X-ray crystal studies

One pot Click chemistry: A three component reaction for the synthesis of 2-mercaptobenzimidazole linked coumarinyl triazoles as anti-tubercular agents

Synthesis of coumarin-theophylline hybrids as a new class of anti-tubercular and anti-microbial agents

Synthesis, antimycobacterial screening and ligand-based molecular docking studies on novel pyrrole derivatives bearing pyrazoline, isoxazole and phenyl thiourea moieties

Synthesis of novel 5-(2,5-bis(2,2,2-trifluoroethoxy)phenyl)-1,3,4-oxadiazole-2-thiol derivatives as potential glucosidase inhibitors

Spectral and molecular modelling studies of sulfadoxine interaction with bovine serum albumin

Interaction of Hydralazine with Human Serum Albumin and Effect of β‑Cyclodextrin on Binding: Insights from Spectroscopic and Molecular Docking Techniques

Synthesis, molecular modeling and BACE-1 inhibitory study of tetrahydrobenzo[b] pyran derivatives

Novel quinoxalinyl chalcone hybrid scaffolds as enoyl ACP reductase inhibitors: Synthesis, molecular docking and biological evaluation

Synthesis, characterization and antitubercular activities of novel pyrrolyl hydrazones and their Cu-complexes

Design, docking analysis, identification, and synthesis of novel 3-(((substituted phenyl) amino)methyl)-2-methylquinazolin-4(3H)-one compounds to fight tuberculosis

Microwave assisted regioselective synthesis of quinoline appended triazoles as potent anti-tubercular and antifungal agents via copper (I) catalyzed cycloaddition

A click chemistry approach for the synthesis of mono and bis aryloxy linked coumarinyl triazoles as anti-tubercular agents

Green synthesis of therapeutically active 1,3,4-oxadiazoles as antioxidants, selective COX-2 inhibitors and their in silico studies

WELPSA: A natural catalyst of alkali and alkaline earth metals for the facile synthesis of tetrahydrobenzo[b]pyrans and pyrano[2,3‐d]pyrimidinones as inhibitors of SARS‐CoV‐2

New thiophene-1,3,4-oxadiazole-thiazolidine-2,4-dione hybrids: Synthesis, MCF-7 inhibition and binding studies

Fluorenone-thiazolidine-4-one scaffolds as antidiabetic and antioxidant agents: design, synthesis, X-ray crystal structures, and binding and computational studies

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