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Radical scavengers as ribonucleotide reductase inhibitors

Current topics in medicinal chemistry, 2012-12, Vol.12 (24), p.2827

2012

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A novel druggable interprotomer pocket in the capsid of rhino- and enteroviruses

PLoS biology, 2019-06, Vol.17 (6), p.e3000281-e3000281

2019

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Ficus religiosa L. bark extracts inhibit human rhinovirus and respiratory syncytial virus infection in vitro

Journal of ethnopharmacology, 2015-12, Vol.176, p.252-257

2015

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Histone deacetylase inhibitors: a review on class-I specific inhibition

Mini reviews in medicinal chemistry, 2015-01, Vol.15 (9), p.731

2015

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Scaffold Based Search on the Desferithiocin Archetype

Mini reviews in medicinal chemistry, 2019-01, Vol.19 (19), p.1564

2019

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Design, synthesis and anticancer activity of piperazine hydroxamates and their histone deacetylase (HDAC) inhibitory activity

Bioorganic & medicinal chemistry letters, 2010-07, Vol.20 (13), p.3906-3910

2010

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Design, synthesis, optimization and antiviral activity of a class of hybrid dengue virus E protein inhibitors

Bioorganic & medicinal chemistry letters, 2015-04, Vol.25 (8), p.1747-1752

2015

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Pyrazoline based MAO inhibitors: Synthesis, biological evaluation and SAR studies

Bioorganic & medicinal chemistry letters, 2011-07, Vol.21 (14), p.4296-4300

2011

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Development of selective and reversible pyrazoline based MAO-A inhibitors: Synthesis, biological evaluation and docking studies

Bioorganic & medicinal chemistry, 2010-03, Vol.18 (5), p.1875-1881

2010

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Comparative Computational Studies on Selective CytochromeP450 1B1 Inhibitors

Bioautomation, 2020-09, Vol.24 (3), p.213-224

2020

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Effect of substitution at N″-position of N′-hydroxy-N-amino guanidines on tumor cell growth

Bioorganic & medicinal chemistry letters, 2012-08, Vol.22 (15), p.4934-4938

2012

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Computer-Aided Structure Based Drug Design Approaches for the Discovery of New Anti-CHIKV Agents

Current computer-aided drug design, 2017-12, Vol.13 (4), p.346

2017

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Crystal structures of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(2,4-di-methyl-phen-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(3-meth-oxy-phen-yl)acetamide

Acta crystallographica. Section E, Crystallographic communications, 2017-07, Vol.73 (Pt 7), p.996-1000

2017

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Crystal structures and Hirshfeld surface analyses of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(pyridin-2-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(pyrazin-2-yl)acetamide

Acta crystallographica. Section E, Crystallographic communications, 2018-05, Vol.74 (Pt 5), p.718-723

2018

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Virtual screening studies on HIV-1 reverse transcriptase inhibitors to design potent leads

European journal of medicinal chemistry, 2011-03, Vol.46 (3), p.851-859

2011

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Crystal structures of N -(4-chloro-phen-yl)-2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]acetamide and N -(3-chloro-phen-yl)-2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]acetamide

Acta crystallographica. Section E, Crystallographic communications, 2017-04, Vol.73 (Pt 4), p.467-471

2017

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Crystal structures of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(naphthalen-1-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(4-fluoro-phen-yl)acetamide

Acta crystallographica. Section E, Crystallographic communications, 2017-02, Vol.73 (Pt 2), p.306-309

2017

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Progress and prospects on DENV protease inhibitors

European journal of medicinal chemistry, 2016-07, Vol.117, p.125-143

2016

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The Mycobactin Biosynthesis Pathway: A Prospective Therapeutic Target in the Battle against Tuberculosis

Journal of medicinal chemistry, 2021-01, Vol.64 (1), p.71-100

2021

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A short survey of dengue protease inhibitor development in the past 6 years (2015–2020) with an emphasis on similarities between DENV and SARS-CoV-2 proteases

Bioorganic & medicinal chemistry, 2021-11, Vol.49, p.116415-116415, Article 116415

2021

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Cink4T, a quinazolinone-based dual inhibitor of Cdk4 and tubulin polymerization, identified via ligand-based virtual screening, for efficient anticancer therapy

European journal of medicinal chemistry, 2019-03, Vol.165, p.115-132

2019

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New chemical constituents from the Piper betle Linn. (Piperaceae)

Natural product research, 2018-05, Vol.32 (9), p.1080-1087

2018

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Thiazolidone derivatives as inhibitors of chikungunya virus

European journal of medicinal chemistry, 2015-01, Vol.89, p.172-178

2015

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The new ether derivative of phenylpropanoid and bioactivity was investigated from the leaves of Piper betle L

Natural product research, 2020-03, Vol.34 (5), p.638-645

2020

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Inhibitors of Human Histone Deacetylase: Synthesis and Enzyme Assay of Hydroxamates with Piperazine Linker

Archiv der Pharmazie (Weinheim), 2010-03, Vol.343 (3), p.167-172

2010

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Radical scavengers as ribonucleotide reductase inhibitors

A novel druggable interprotomer pocket in the capsid of rhino- and enteroviruses

Ficus religiosa L. bark extracts inhibit human rhinovirus and respiratory syncytial virus infection in vitro

Histone deacetylase inhibitors: a review on class-I specific inhibition

Scaffold Based Search on the Desferithiocin Archetype

Design, synthesis and anticancer activity of piperazine hydroxamates and their histone deacetylase (HDAC) inhibitory activity

Design, synthesis, optimization and antiviral activity of a class of hybrid dengue virus E protein inhibitors

Pyrazoline based MAO inhibitors: Synthesis, biological evaluation and SAR studies

Development of selective and reversible pyrazoline based MAO-A inhibitors: Synthesis, biological evaluation and docking studies

Comparative Computational Studies on Selective CytochromeP450 1B1 Inhibitors

Effect of substitution at N″-position of N′-hydroxy-N-amino guanidines on tumor cell growth

Computer-Aided Structure Based Drug Design Approaches for the Discovery of New Anti-CHIKV Agents

Crystal structures of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(2,4-di-methyl-phen-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(3-meth-oxy-phen-yl)acetamide

Crystal structures and Hirshfeld surface analyses of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(pyridin-2-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(pyrazin-2-yl)acetamide

Virtual screening studies on HIV-1 reverse transcriptase inhibitors to design potent leads

Crystal structures of N -(4-chloro-phen-yl)-2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]acetamide and N -(3-chloro-phen-yl)-2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]acetamide

Crystal structures of 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(naphthalen-1-yl)acetamide and 2-[(4,6-di-amino-pyrimidin-2-yl)sulfan-yl]- N -(4-fluoro-phen-yl)acetamide

Progress and prospects on DENV protease inhibitors

The Mycobactin Biosynthesis Pathway: A Prospective Therapeutic Target in the Battle against Tuberculosis

A short survey of dengue protease inhibitor development in the past 6 years (2015–2020) with an emphasis on similarities between DENV and SARS-CoV-2 proteases

Cink4T, a quinazolinone-based dual inhibitor of Cdk4 and tubulin polymerization, identified via ligand-based virtual screening, for efficient anticancer therapy

New chemical constituents from the Piper betle Linn. (Piperaceae)

Thiazolidone derivatives as inhibitors of chikungunya virus

The new ether derivative of phenylpropanoid and bioactivity was investigated from the leaves of Piper betle L

Inhibitors of Human Histone Deacetylase: Synthesis and Enzyme Assay of Hydroxamates with Piperazine Linker

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