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Exploration of metal-organic framework MOF-177 coated fibers for headspace solid-phase microextraction of polychlorinated biphenyls and polycyclic aromatic hydrocarbons

Talanta (Oxford), 2015-11, Vol.144, p.369-374

2015

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One-pot cascade synthesis of N-methoxyisoquinolinediones via Rh(III)-catalyzed carbenoid insertion C-H activation/cyclization

Chemical communications (Cambridge, England), 2015-01, Vol.51 (4), p.668-671

2015

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Study on the design, synthesis and structure-activity relationships of new thiosemicarbazone compounds as tyrosinase inhibitors

European journal of medicinal chemistry, 2017-10, Vol.139, p.815-825

2017

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The Ag–BiOBrxI1−x composite photocatalyst: Preparation, characterization and their novel pollutants removal property

Applied surface science, 2013-08, Vol.279, p.374-379

2013

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Structure-based modification of 3-/4-aminoacetophenones giving a profound change of activity on tyrosinase: From potent activators to highly efficient inhibitors

European journal of medicinal chemistry, 2015-03, Vol.93, p.255-262

2015

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Design, synthesis and 3D-QSAR of β-carboline derivatives as potent antitumor agents

European journal of medicinal chemistry, 2010-06, Vol.45 (6), p.2503-2515

2010

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Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors

European journal of medicinal chemistry, 2010-02, Vol.45 (2), p.639-646

2010

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Biological evaluations of novel vitamin C esters as mushroom tyrosinase inhibitors and antioxidants

Food chemistry, 2009-12, Vol.117 (3), p.381-386

2009

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Synthesis and biological evaluation of 1,9-disubstituted β-carbolines as potent DNA intercalating and cytotoxic agents

European journal of medicinal chemistry, 2011-10, Vol.46 (10), p.5127-5137

2011

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Inhibitory effects of 5-benzylidene barbiturate derivatives on mushroom tyrosinase and their antibacterial activities

European journal of medicinal chemistry, 2009-10, Vol.44 (10), p.4235-4243

2009

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Design, synthesis and evaluation of N13-substituted evodiamine derivatives against human cancer cell lines

Molecules (Basel, Switzerland), 2013-12, Vol.18 (12), p.15750-15768

2013

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Refinement of arylthiosemicarbazone pharmacophore in inhibition of mushroom tyrosinase

European journal of medicinal chemistry, 2011-09, Vol.46 (9), p.4330-4335

2011

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A Facile and Efficient Oxalyldihydrazide/Ketone‐Promoted Copper‐Catalyzed Amination of Aryl Halides in Water

European Journal of Organic Chemistry, 2009-02, Vol.2009 (5), p.635-642

2009

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Synthesis and cytotoxicity of 17a-aza- d-homo-androster-17-one derivatives

Bioorganic & medicinal chemistry letters, 2011-06, Vol.21 (12), p.3641-3643

2011

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A class of potent tyrosinase inhibitors: Alkylidenethiosemicarbazide compounds

European journal of medicinal chemistry, 2009-04, Vol.44 (4), p.1773-1778

2009

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Synthesis and neuroprotective action of xyloketal derivatives in Parkinson's disease models

Marine drugs, 2013-12, Vol.11 (12), p.5159-5189

2013

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Synthesis, cytotoxic activities and DNA binding properties of β-carboline derivatives

European journal of medicinal chemistry, 2010-11, Vol.45 (11), p.4740-4745

2010

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Preclinical Study of Novel Curcumin Analogue SSC-5 Using Orthotopic Tumor Xenograft Model for Esophageal Squamous Cell Carcinoma

Cancer Research and Treatment, 2018, 50(4), , pp.1362-1377

2018

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Synthesis and evaluation of 5-benzylidene(thio)barbiturate-β-d-glycosides as mushroom tyrosinase inhibitors

Bioorganic & medicinal chemistry letters, 2009-08, Vol.19 (15), p.4055-4058

2009

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Synthesis and evaluation of some new aza-B-homocholestane derivatives as anticancer agents

Marine drugs, 2014-03, Vol.12 (4), p.1715-1731

2014

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Synthesis and evaluation of some 17-acetamidoandrostane and N,N-dimethyl-7-deoxycholic amide derivatives as cytotoxic agents: structure/activity studies

Molecules (Basel, Switzerland), 2013-06, Vol.18 (7), p.7436-7447

2013

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Synthesis of novel β-carbolines with efficient DNA-binding capacity and potent cytotoxicity

Bioorganic & medicinal chemistry letters, 2010-07, Vol.20 (13), p.3876-3879

2010

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Synthesis and in vitro cytotoxic evaluation of novel 3,4,5-trimethoxyphenyl substituted β-carboline derivatives

European journal of medicinal chemistry, 2009-02, Vol.44 (2), p.533-540

2009

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Synthesis of 4-[(diethylamino)methyl]-phenol derivatives as novel cholinesterase inhibitors with selectivity towards butyrylcholinesterase

Bioorganic & medicinal chemistry letters, 2010-06, Vol.20 (11), p.3254-3258

2010

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Synthesis and biological evaluation of helicid analogues as mushroom tyrosinase inhibitors

Bioorganic & medicinal chemistry, 2008-12, Vol.18 (24), p.6490-6493

2008

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Exploration of metal-organic framework MOF-177 coated fibers for headspace solid-phase microextraction of polychlorinated biphenyls and polycyclic aromatic hydrocarbons

One-pot cascade synthesis of N-methoxyisoquinolinediones via Rh(III)-catalyzed carbenoid insertion C-H activation/cyclization

Study on the design, synthesis and structure-activity relationships of new thiosemicarbazone compounds as tyrosinase inhibitors

The Ag–BiOBrxI1−x composite photocatalyst: Preparation, characterization and their novel pollutants removal property

Structure-based modification of 3-/4-aminoacetophenones giving a profound change of activity on tyrosinase: From potent activators to highly efficient inhibitors

Design, synthesis and 3D-QSAR of β-carboline derivatives as potent antitumor agents

Synthesis and biological evaluation of novel 4-hydroxybenzaldehyde derivatives as tyrosinase inhibitors

Biological evaluations of novel vitamin C esters as mushroom tyrosinase inhibitors and antioxidants

Synthesis and biological evaluation of 1,9-disubstituted β-carbolines as potent DNA intercalating and cytotoxic agents

Inhibitory effects of 5-benzylidene barbiturate derivatives on mushroom tyrosinase and their antibacterial activities

Design, synthesis and evaluation of N13-substituted evodiamine derivatives against human cancer cell lines

Refinement of arylthiosemicarbazone pharmacophore in inhibition of mushroom tyrosinase

A Facile and Efficient Oxalyldihydrazide/Ketone‐Promoted Copper‐Catalyzed Amination of Aryl Halides in Water

Synthesis and cytotoxicity of 17a-aza- d-homo-androster-17-one derivatives

A class of potent tyrosinase inhibitors: Alkylidenethiosemicarbazide compounds

Synthesis and neuroprotective action of xyloketal derivatives in Parkinson's disease models

Synthesis, cytotoxic activities and DNA binding properties of β-carboline derivatives

Preclinical Study of Novel Curcumin Analogue SSC-5 Using Orthotopic Tumor Xenograft Model for Esophageal Squamous Cell Carcinoma

Synthesis and evaluation of 5-benzylidene(thio)barbiturate-β-d-glycosides as mushroom tyrosinase inhibitors

Synthesis and evaluation of some new aza-B-homocholestane derivatives as anticancer agents

Synthesis and evaluation of some 17-acetamidoandrostane and N,N-dimethyl-7-deoxycholic amide derivatives as cytotoxic agents: structure/activity studies

Synthesis of novel β-carbolines with efficient DNA-binding capacity and potent cytotoxicity

Synthesis and in vitro cytotoxic evaluation of novel 3,4,5-trimethoxyphenyl substituted β-carboline derivatives

Synthesis of 4-[(diethylamino)methyl]-phenol derivatives as novel cholinesterase inhibitors with selectivity towards butyrylcholinesterase

Synthesis and biological evaluation of helicid analogues as mushroom tyrosinase inhibitors

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