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A molecular mechanism of artemisinin resistance in Plasmodium falciparum malaria

Nature (London), 2015-04, Vol.520 (7549), p.683-687

2015

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Mechanism, Reactivity, and Selectivity in Palladium-Catalyzed Redox-Relay Heck Arylations of Alkenyl Alcohols

Journal of the American Chemical Society, 2014-02, Vol.136 (5), p.1960-1967

2014

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Computational Exploration of Zinc Binding Groups for HDAC Inhibition

Journal of organic chemistry, 2013-05, Vol.78 (10), p.5051-5055

2013

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Inhibition and Mechanism of HDAC8 Revisited

Journal of the American Chemical Society, 2014-08, Vol.136 (33), p.11636-11643

2014

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The Increasingly Complex Mechanism of HMG-CoA Reductase

Accounts of chemical research, 2013-11, Vol.46 (11), p.2416-2426

2013

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Diastereoselectivity in Lewis-Acid-Catalyzed Mukaiyama Aldol Reactions: A DFT Study

Journal of the American Chemical Society, 2012-09, Vol.134 (36), p.14973-14981

2012

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Toward Selective Histone Deacetylase Inhibitor Design: Homology Modeling, Docking Studies, and Molecular Dynamics Simulations of Human Class I Histone Deacetylases

Journal of medicinal chemistry, 2005-11, Vol.48 (22), p.6936-6947

2005

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Synthesis and Conformation−Activity Relationships of the Peptide Isosteres of FK228 and Largazole

Journal of the American Chemical Society, 2009-03, Vol.131 (8), p.2900-2905

2009

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Synthesis and Histone Deacetylase Inhibitory Activity of Largazole Analogs: Alteration of the Zinc-Binding Domain and Macrocyclic Scaffold

Organic letters, 2009-03, Vol.11 (6), p.1301-1304

2009

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Identifying ligand binding conformations of the β2-adrenergic receptor by using its agonists as computational probes

PloS one, 2012-12, Vol.7 (12), p.e50186

2012

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Molecular Modeling of the Reaction Pathway and Hydride Transfer Reactions of HMG-CoA Reductase

Biochemistry (Easton), 2012-10, Vol.51 (40), p.7983-7995

2012

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Mild and Efficient Desymmetrization of Diynes via Hydroamination: Application to the Synthesis of (±)-Monomorine I

Journal of organic chemistry, 2010-02, Vol.75 (4), p.1325-1328

2010

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Structure and Reactivity of Radical Ions: New Twists on Old Concepts

Chemistry : a European journal, 2006-09, Vol.12 (27), p.7018-7026

2006

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Mechanism of Hydroxyl Radical-Induced Breakdown of the Herbicide 2,4-Dichlorophenoxyacetic Acid (2,4-D)

Chemistry : a European journal, 2003-11, Vol.9 (21), p.5379-5387

2003

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Computational Studies of the Cholesterol Transport between NPC2 and the N‑Terminal Domain of NPC1 (NPC1(NTD))

Biochemistry (Easton), 2013-10, Vol.52 (39), p.6879-6891

2013

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Isotope Effects on the Enzymatic and Nonenzymatic Reactions of Chorismate

Journal of the American Chemical Society, 2005-09, Vol.127 (37), p.12957-12964

2005

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Synthesis, Structure, and Metal Complexation Behavior of a New Type of Functionalized Chiral Phenanthroline Derivative

Journal of organic chemistry, 2008-05, Vol.73 (10), p.3911-3914

2008

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Metal-Templated Design: Enantioselective Hydrogen-Bond-Driven Catalysis Requiring Only Parts-per-Million Catalyst Loading

Journal of the American Chemical Society, 2016-07, Vol.138 (28), p.8774-8780

2016

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Selective inhibition of BET bromodomains

Nature (London), 2010-12, Vol.468 (7327), p.1067-1073

2010

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Isotope Effects and the Mechanism of an Electron-Transfer-Catalyzed Diels−Alder Reaction

Journal of the American Chemical Society, 2002-09, Vol.124 (38), p.11552-11559

2002

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Variable Active Site Loop Conformations Accommodate the Binding of Macrocyclic Largazole Analogues to HDAC8

Biochemistry (Easton), 2015-03, Vol.54 (12), p.2126-2135

2015

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Zinc Binding in HDAC Inhibitors: A DFT Study

Journal of organic chemistry, 2007-07, Vol.72 (14), p.5446-5449

2007

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The cytoplasmic prolyl-tRNA synthetase of the malaria parasite is a dual-stage target of febrifugine and its analogs

Science translational medicine, 2015-05, Vol.7 (288), p.288ra77

2015

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Structural Origin of Selectivity in Class II-Selective Histone Deacetylase Inhibitors

Journal of medicinal chemistry, 2008-05, Vol.51 (10), p.2898-2906

2008

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Conformational and SAR analysis of NAALADase and PSMA inhibitors

Bioorganic & medicinal chemistry, 2003-10, Vol.11 (20), p.4455-4461

2003

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A molecular mechanism of artemisinin resistance in Plasmodium falciparum malaria

Mechanism, Reactivity, and Selectivity in Palladium-Catalyzed Redox-Relay Heck Arylations of Alkenyl Alcohols

Computational Exploration of Zinc Binding Groups for HDAC Inhibition

Inhibition and Mechanism of HDAC8 Revisited

The Increasingly Complex Mechanism of HMG-CoA Reductase

Diastereoselectivity in Lewis-Acid-Catalyzed Mukaiyama Aldol Reactions: A DFT Study

Toward Selective Histone Deacetylase Inhibitor Design: Homology Modeling, Docking Studies, and Molecular Dynamics Simulations of Human Class I Histone Deacetylases

Synthesis and Conformation−Activity Relationships of the Peptide Isosteres of FK228 and Largazole

Synthesis and Histone Deacetylase Inhibitory Activity of Largazole Analogs: Alteration of the Zinc-Binding Domain and Macrocyclic Scaffold

Identifying ligand binding conformations of the β2-adrenergic receptor by using its agonists as computational probes

Molecular Modeling of the Reaction Pathway and Hydride Transfer Reactions of HMG-CoA Reductase

Mild and Efficient Desymmetrization of Diynes via Hydroamination: Application to the Synthesis of (±)-Monomorine I

Structure and Reactivity of Radical Ions: New Twists on Old Concepts

Mechanism of Hydroxyl Radical-Induced Breakdown of the Herbicide 2,4-Dichlorophenoxyacetic Acid (2,4-D)

Computational Studies of the Cholesterol Transport between NPC2 and the N‑Terminal Domain of NPC1 (NPC1(NTD))

Isotope Effects on the Enzymatic and Nonenzymatic Reactions of Chorismate

Synthesis, Structure, and Metal Complexation Behavior of a New Type of Functionalized Chiral Phenanthroline Derivative

Metal-Templated Design: Enantioselective Hydrogen-Bond-Driven Catalysis Requiring Only Parts-per-Million Catalyst Loading

Selective inhibition of BET bromodomains

Isotope Effects and the Mechanism of an Electron-Transfer-Catalyzed Diels−Alder Reaction

Variable Active Site Loop Conformations Accommodate the Binding of Macrocyclic Largazole Analogues to HDAC8

Zinc Binding in HDAC Inhibitors: A DFT Study

The cytoplasmic prolyl-tRNA synthetase of the malaria parasite is a dual-stage target of febrifugine and its analogs

Structural Origin of Selectivity in Class II-Selective Histone Deacetylase Inhibitors

Conformational and SAR analysis of NAALADase and PSMA inhibitors

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