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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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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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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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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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Progress and prospects on DENV protease inhibitors

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

2016

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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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Thiazolidone derivatives as inhibitors of chikungunya virus

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

2015

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Phytoestrogens and their synthetic analogues as substrate mimic inhibitors of CYP1B1

European journal of medicinal chemistry, 2019-02, Vol.163, p.28-36

2019

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Synthesis and molecular modelling studies of novel sulphonamide derivatives as dengue virus 2 protease inhibitors

Bioorganic chemistry, 2015-10, Vol.62, p.74-82

2015

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Fragment and knowledge-based design of selective GSK-3β inhibitors using virtual screening models

European journal of medicinal chemistry, 2009-06, Vol.44 (6), p.2361-2371

2009

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A novel N-hydroxy-N′-aminoguanidine derivative inhibits ribonucleotide reductase activity: Effects in human HL-60 promyelocytic leukemia cells and synergism with arabinofuranosylcytosine (Ara-C)

Biochemical pharmacology, 2011-01, Vol.81 (1), p.50-59

2011

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Fragment and knowledge-based design of selective GSK-3beta inhibitors using virtual screening models

European journal of medicinal chemistry, 2009-06, Vol.44 (6), p.2361-2371

2009

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

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

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

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

Progress and prospects on DENV protease inhibitors

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

Thiazolidone derivatives as inhibitors of chikungunya virus

Phytoestrogens and their synthetic analogues as substrate mimic inhibitors of CYP1B1

Synthesis and molecular modelling studies of novel sulphonamide derivatives as dengue virus 2 protease inhibitors

Fragment and knowledge-based design of selective GSK-3β inhibitors using virtual screening models

A novel N-hydroxy-N′-aminoguanidine derivative inhibits ribonucleotide reductase activity: Effects in human HL-60 promyelocytic leukemia cells and synergism with arabinofuranosylcytosine (Ara-C)

Fragment and knowledge-based design of selective GSK-3beta inhibitors using virtual screening models

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