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Ionic-Liquid-Supported Synthesis: A Novel Liquid-Phase Strategy for Organic Synthesis

Accounts of chemical research, 2006-12, Vol.39 (12), p.897-908

2006

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Aerobic and Electrochemical Oxidative Cross-Dehydrogenative-Coupling (CDC) Reaction in an Imidazolium-Based Ionic Liquid

Chemistry : a European journal, 2010-07, Vol.16 (27), p.8162-8166

2010

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Rational design of berberine-based FtsZ inhibitors with broad-spectrum antibacterial activity

PloS one, 2014-05, Vol.9 (5), p.e97514-e97514

2014

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A novel prodrug of epigallocatechin-3-gallate: differential epigenetic hTERT repression in human breast cancer cells

Cancer prevention research (Philadelphia, Pa.), 2011-08, Vol.4 (8), p.1243-1254

2011

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A novel prodrug of the green tea polyphenol (-)-epigallocatechin-3-gallate as a potential anticancer agent

Cancer research (Chicago, Ill.), 2007-05, Vol.67 (9), p.4303-4310

2007

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Targeting tumor ubiquitin-proteasome pathway with polyphenols for chemosensitization

Anti-cancer agents in medicinal chemistry, 2012-10, Vol.12 (8), p.891-901

2012

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Biological and Mechanistic Characterization of Novel Prodrugs of Green Tea Polyphenol Epigallocatechin Gallate Analogs in Human Leiomyoma Cell Lines

Journal of cellular biochemistry, 2016-10, Vol.117 (10), p.2357-2369

2016

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Organic syntheses using indium-mediated and catalyzed reactions in aqueous media

Tetrahedron, 1999-09, Vol.55 (37), p.11149-11176

1999

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Targeting the DNA Repair Endonuclease ERCC1-XPF with Green Tea Polyphenol Epigallocatechin-3-Gallate (EGCG) and Its Prodrug to Enhance Cisplatin Efficacy in Human Cancer Cells

Nutrients, 2018-11, Vol.10 (11), p.1644

2018

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Dibenzoate esters of cis‐tetralin‐2,3‐diol as analogs of (–)‐epigallocatechin gallate: synthesis and crystal structure of anticancer drug candidates

Acta crystallographica. Section C, Crystal structure communications, 2020-12, Vol.76 (12), p.1085-1095

2020

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Modulation of Multidrug Resistance Protein 1 (MRP1/ABCC1)-Mediated Multidrug Resistance by Bivalent Apigenin Homodimers and Their Derivatives

Journal of medicinal chemistry, 2009-09, Vol.52 (17), p.5311-5322

2009

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Ionic-Liquid-Supported Organocatalyst: Efficient and Recyclable Ionic-Liquid-Anchored Proline for Asymmetric Aldol Reaction

Advanced synthesis & catalysis, 2006-08, Vol.348 (12-13), p.1711-1718

2006

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(-)-Epiafzelechin Protects against Ovariectomy-induced Bone Loss in Adult Mice and Modulate Osteoblastic and Osteoclastic Functions In Vitro

Nutrients, 2017-05, Vol.9 (5), p.530

2017

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Comprehensive organic reactions in aqueous media

2nd ed., 2007

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Ebselen as a potent covalent inhibitor of New Delhi metallo-β-lactamase (NDM-1)

Chemical communications (Cambridge, England), 2015-06, Vol.51 (46), p.9543-9546

2015

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Docking studies and model development of tea polyphenol proteasome inhibitors: Applications to rational drug design

Proteins, structure, function, and bioinformatics, 2004-01, Vol.54 (1), p.58-70

2004

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Zwitterionic Phosphonium Sulfonates as Easily Phase-Separable Ion-Tagged Wittig Reagents

Journal of organic chemistry, 2008-11, Vol.73 (21), p.8583-8586

2008

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Design, synthesis and antibacterial evaluation of 2,4-disubstituted-6-thiophenyl-pyrimidines

European journal of medicinal chemistry, 2019-01, Vol.161, p.141-153

2019

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Lessons from Nature: Sources and Strategies for Developing AMPK Activators for Cancer Chemotherapeutics

Anti-cancer agents in medicinal chemistry, 2015-01, Vol.15 (5), p.657-671

2015

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Synthetic and Mechanistic Studies of Indium-Mediated Allylation of Imines in Ionic Liquids

Journal of organic chemistry, 2007-02, Vol.72 (3), p.923-929

2007

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Perspectives on the recent developments with green tea polyphenols in drug discovery

Expert opinion on drug discovery, 2018-07, Vol.13 (7), p.643-660

2018

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Investigation of synergistic antimicrobial effects of the drug combinations of meropenem and 1,2-benzisoselenazol-3(2H)-one derivatives on carbapenem-resistant Enterobacteriaceae producing NDM-1

European journal of medicinal chemistry, 2018-07, Vol.155, p.285-302

2018

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Study of the green tea polyphenols catechin-3-gallate (CG) and epicatechin-3-gallate (ECG) as proteasome inhibitors

Bioorganic & medicinal chemistry, 2004-07, Vol.12 (13), p.3521-3527

2004

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Flavonoid dimers are highly potent killers of multidrug resistant cancer cells overexpressing MRP1

Biochemical pharmacology, 2017-01, Vol.124, p.10-18

2017

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Therapeutic potential of a novel prodrug of green tea extract in induction of apoptosis via ERK/JNK and Akt signaling pathway in human endometrial cancer

BMC cancer, 2020-10, Vol.20 (1), p.964-964, Article 964

2020

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Ionic-Liquid-Supported Synthesis: A Novel Liquid-Phase Strategy for Organic Synthesis

Aerobic and Electrochemical Oxidative Cross-Dehydrogenative-Coupling (CDC) Reaction in an Imidazolium-Based Ionic Liquid

Rational design of berberine-based FtsZ inhibitors with broad-spectrum antibacterial activity

A novel prodrug of epigallocatechin-3-gallate: differential epigenetic hTERT repression in human breast cancer cells

A novel prodrug of the green tea polyphenol (-)-epigallocatechin-3-gallate as a potential anticancer agent

Targeting tumor ubiquitin-proteasome pathway with polyphenols for chemosensitization

Biological and Mechanistic Characterization of Novel Prodrugs of Green Tea Polyphenol Epigallocatechin Gallate Analogs in Human Leiomyoma Cell Lines

Organic syntheses using indium-mediated and catalyzed reactions in aqueous media

Targeting the DNA Repair Endonuclease ERCC1-XPF with Green Tea Polyphenol Epigallocatechin-3-Gallate (EGCG) and Its Prodrug to Enhance Cisplatin Efficacy in Human Cancer Cells

Dibenzoate esters of cis‐tetralin‐2,3‐diol as analogs of (–)‐epigallocatechin gallate: synthesis and crystal structure of anticancer drug candidates

Modulation of Multidrug Resistance Protein 1 (MRP1/ABCC1)-Mediated Multidrug Resistance by Bivalent Apigenin Homodimers and Their Derivatives

Ionic-Liquid-Supported Organocatalyst: Efficient and Recyclable Ionic-Liquid-Anchored Proline for Asymmetric Aldol Reaction

(-)-Epiafzelechin Protects against Ovariectomy-induced Bone Loss in Adult Mice and Modulate Osteoblastic and Osteoclastic Functions In Vitro

Comprehensive organic reactions in aqueous media

Ebselen as a potent covalent inhibitor of New Delhi metallo-β-lactamase (NDM-1)

Docking studies and model development of tea polyphenol proteasome inhibitors: Applications to rational drug design

Zwitterionic Phosphonium Sulfonates as Easily Phase-Separable Ion-Tagged Wittig Reagents

Design, synthesis and antibacterial evaluation of 2,4-disubstituted-6-thiophenyl-pyrimidines

Lessons from Nature: Sources and Strategies for Developing AMPK Activators for Cancer Chemotherapeutics

Synthetic and Mechanistic Studies of Indium-Mediated Allylation of Imines in Ionic Liquids

Perspectives on the recent developments with green tea polyphenols in drug discovery

Investigation of synergistic antimicrobial effects of the drug combinations of meropenem and 1,2-benzisoselenazol-3(2H)-one derivatives on carbapenem-resistant Enterobacteriaceae producing NDM-1

Study of the green tea polyphenols catechin-3-gallate (CG) and epicatechin-3-gallate (ECG) as proteasome inhibitors

Flavonoid dimers are highly potent killers of multidrug resistant cancer cells overexpressing MRP1

Therapeutic potential of a novel prodrug of green tea extract in induction of apoptosis via ERK/JNK and Akt signaling pathway in human endometrial cancer

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