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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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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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Rh(III)-catalyzed and alcohol-involved carbenoid C-H insertion into N-phenoxyacetamides using α-diazomalonates

Chemical communications (Cambridge, England), 2015-04, Vol.51 (27), p.5868-5871

2015

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1-(1-Arylethylidene)thiosemicarbazide derivatives: A new class of tyrosinase inhibitors

Bioorganic & medicinal chemistry, 2008-02, Vol.16 (3), p.1096-1102

2008

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Prebiotically Plausible RNA Activation Compatible with Ribozyme‐Catalyzed Ligation

Angewandte Chemie International Edition, 2021-02, Vol.60 (6), p.2952-2957

International ed. in English, 2021

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Concurrent Prebiotic Formation of Nucleoside‐Amidophosphates and Nucleoside‐Triphosphates Potentiates Transition from Abiotic to Biotic Polymerization

Angewandte Chemie International Edition, 2022-01, Vol.61 (1), p.e202113625-n/a

International ed. in English, 2022

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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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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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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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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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Design, synthesis and biological evaluation of hydroxy- or methoxy-substituted 5-benzylidene(thio) barbiturates as novel tyrosinase inhibitors

Bioorganic & medicinal chemistry, 2014-07, Vol.22 (13), p.3279-3284

2014

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Rational design, synthesis and structure–activity relationships of 4-alkoxy- and 4-acyloxy-phenylethylenethiosemicarbazone analogues as novel tyrosinase inhibitors

Bioorganic & medicinal chemistry, 2015-03, Vol.23 (5), p.924-931

2015

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Dual In-Tether Chiral Centers Modulate Peptide Helicity

Bioconjugate chemistry, 2017-05, Vol.28 (5), p.1537-1543

2017

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Design, synthesis and in vitro and in vivo antitumor activities of novel bivalent β-carbolines

European journal of medicinal chemistry, 2013-02, Vol.60, p.10-22

2013

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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 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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An in-tether sulfilimine chiral center induces β-turn conformation in short peptides

Organic & biomolecular chemistry, 2016-01, Vol.14 (42), p.9993-9999

2016

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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 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, 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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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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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

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

Rh(III)-catalyzed and alcohol-involved carbenoid C-H insertion into N-phenoxyacetamides using α-diazomalonates

1-(1-Arylethylidene)thiosemicarbazide derivatives: A new class of tyrosinase inhibitors

Prebiotically Plausible RNA Activation Compatible with Ribozyme‐Catalyzed Ligation

Concurrent Prebiotic Formation of Nucleoside‐Amidophosphates and Nucleoside‐Triphosphates Potentiates Transition from Abiotic to Biotic Polymerization

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

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

Refinement of arylthiosemicarbazone pharmacophore in inhibition of mushroom tyrosinase

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

Design, synthesis and biological evaluation of hydroxy- or methoxy-substituted 5-benzylidene(thio) barbiturates as novel tyrosinase inhibitors

Rational design, synthesis and structure–activity relationships of 4-alkoxy- and 4-acyloxy-phenylethylenethiosemicarbazone analogues as novel tyrosinase inhibitors

Dual In-Tether Chiral Centers Modulate Peptide Helicity

Design, synthesis and in vitro and in vivo antitumor activities of novel bivalent β-carbolines

A class of potent tyrosinase inhibitors: Alkylidenethiosemicarbazide compounds

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

An in-tether sulfilimine chiral center induces β-turn conformation in short peptides

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

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

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

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

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