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Structural basis for backbone N-methylation by an interrupted adenylation domain

Nature chemical biology, 2018-05, Vol.14 (5), p.428-430

2018

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A Catalytic Asymmetric Chlorocyclization of Unsaturated Amides

Angewandte Chemie (International ed.), 2011-03, Vol.50 (11), p.2593-2596

International ed. in English, 2011

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Pyrimidone inhibitors targeting Chikungunya Virus nsP3 macrodomain by fragment-based drug design

PloS one, 2021-01, Vol.16 (1), p.e0245013

2021

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Solvent-Dependent Enantiodivergence in the Chlorocyclization of Unsaturated Carbamates

Chemistry : a European journal, 2013-07, Vol.19 (27), p.9015-9021

2013

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Activation and Loading of the Starter Unit during Thiocoraline Biosynthesis

Biochemistry (Easton), 2017-08, Vol.56 (34), p.4457-4467

2017

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Enzymatic Evidence for a Revised Congocidine Biosynthetic Pathway

Chembiochem : a European journal of chemical biology, 2015-06, Vol.16 (9), p.1307-1313

2015

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Interfering With DNA Decondensation as a Strategy Against Mycobacteria

Frontiers in microbiology, 2018-09, Vol.9, p.2034-2034

2018

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Novel alkylated azoles as potent antifungals

European journal of medicinal chemistry, 2017-06, Vol.133, p.309-318

2017

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Deciphering Nature’s Intricate Way of N,S-Dimethylating l‑Cysteine: Sequential Action of Two Bifunctional Adenylation Domains

Biochemistry (Easton), 2017-11, Vol.56 (46), p.6087-6097

2017

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Repurposing antipsychotic drugs into antifungal agents: Synergistic combinations of azoles and bromperidol derivatives in the treatment of various fungal infections

European journal of medicinal chemistry, 2017-10, Vol.139, p.12-21

2017

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Discovery of substituted benzyloxy-benzylamine inhibitors of acetyltransferase Eis and their anti-mycobacterial activity

European journal of medicinal chemistry, 2022-11, Vol.242, p.114698, Article 114698

2022

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Sulfonamide-Based Inhibitors of Aminoglycoside Acetyltransferase Eis Abolish Resistance to Kanamycin in Mycobacterium tuberculosis

Journal of medicinal chemistry, 2016-12, Vol.59 (23), p.10619-10628

2016

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Highly Efficient Halogenation of Organic Compounds with Halides Catalyzed by Cerium(III) Chloride Heptahydrate Using Hydrogen Peroxide as the Terminal Oxidant in Water

Advanced synthesis & catalysis, 2009-08, Vol.351 (11-12), p.1925-1932

2009

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A Catalytic Asymmetric Chlorocyclization of Unsaturated Amides

Angewandte Chemie, 2011-03, Vol.123 (11), p.2641-2644

2011

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Structure-based design of haloperidol analogues as inhibitors of acetyltransferase Eis from Mycobacterium tuberculosis to overcome kanamycin resistance

RSC medicinal chemistry, 2021-11, Vol.12 (11), p.1894-1909

2021

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Optimization of pyrazole-containing 1,2,4-triazolo-[3,4-b]thiadiazines, a new class of STAT3 pathway inhibitors

Bioorganic & medicinal chemistry letters, 2016-08, Vol.26 (15), p.3581-3585

2016

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Pronounced Catalytic Effect of Micellar Solution of Sodium Dodecyl Sulfate (SDS) for Regioselective Iodination of Aromatic Compounds with a Sodium Iodide/Cerium(IV) Trihydroxide Hydroperoxide System

Advanced synthesis & catalysis, 2005-12, Vol.347 (15), p.1925-1928

2005

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Discovery of Allosteric and Selective Inhibitors of Inorganic Pyrophosphatase from Mycobacterium tuberculosis

ACS chemical biology, 2016-11, Vol.11 (11), p.3084-3092

2016

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Discovery and Optimization of Two Eis Inhibitor Families as Kanamycin Adjuvants against Drug-Resistant M. tuberculosis

ACS medicinal chemistry letters, 2016-12, Vol.7 (12), p.1219-1221

2016

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Discovery and Optimization of 6‑(1-Substituted pyrrole-2-yl)‑s‑triazine Containing Compounds as Antibacterial Agents

ACS infectious diseases, 2022-04, Vol.8 (4), p.757-767

2022

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Combating Enhanced Intracellular Survival (Eis)-Mediated Kanamycin Resistance of Mycobacterium tuberculosis by Novel Pyrrolo[1,5‑a]pyrazine-Based Eis Inhibitors

ACS infectious diseases, 2017-04, Vol.3 (4), p.302-309

2017

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Structure-based design of haloperidol analogues as inhibitors of acetyltransferase Eis from to overcome kanamycin resistance

RSC medicinal chemistry, 2021-11, Vol.12 (11), p.1894-199

2021

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Potent 1,2,4-Triazino[5,6b]indole-3-thioether Inhibitors of the Kanamycin Resistance Enzyme Eis from Mycobacterium tuberculosis

ACS infectious diseases, 2018-06, Vol.4 (6), p.1030-1040

2018

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A Minimalist NMR Approach for the Structural Revision of Mucoxin

Chemistry : a European journal, 2010-12, Vol.16 (46), p.13749-13756

2010

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Inside Cover: A Minimalist NMR Approach for the Structural Revision of Mucoxin (Chem. Eur. J. 46/2010)

Chemistry : a European journal, 2010-12, Vol.16 (46), p.13554-13554

2010

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Structural basis for backbone N-methylation by an interrupted adenylation domain

A Catalytic Asymmetric Chlorocyclization of Unsaturated Amides

Pyrimidone inhibitors targeting Chikungunya Virus nsP3 macrodomain by fragment-based drug design

Solvent-Dependent Enantiodivergence in the Chlorocyclization of Unsaturated Carbamates

Activation and Loading of the Starter Unit during Thiocoraline Biosynthesis

Enzymatic Evidence for a Revised Congocidine Biosynthetic Pathway

Interfering With DNA Decondensation as a Strategy Against Mycobacteria

Novel alkylated azoles as potent antifungals

Deciphering Nature’s Intricate Way of N,S-Dimethylating l‑Cysteine: Sequential Action of Two Bifunctional Adenylation Domains

Repurposing antipsychotic drugs into antifungal agents: Synergistic combinations of azoles and bromperidol derivatives in the treatment of various fungal infections

Discovery of substituted benzyloxy-benzylamine inhibitors of acetyltransferase Eis and their anti-mycobacterial activity

Sulfonamide-Based Inhibitors of Aminoglycoside Acetyltransferase Eis Abolish Resistance to Kanamycin in Mycobacterium tuberculosis

Highly Efficient Halogenation of Organic Compounds with Halides Catalyzed by Cerium(III) Chloride Heptahydrate Using Hydrogen Peroxide as the Terminal Oxidant in Water

A Catalytic Asymmetric Chlorocyclization of Unsaturated Amides

Structure-based design of haloperidol analogues as inhibitors of acetyltransferase Eis from Mycobacterium tuberculosis to overcome kanamycin resistance

Optimization of pyrazole-containing 1,2,4-triazolo-[3,4-b]thiadiazines, a new class of STAT3 pathway inhibitors

Pronounced Catalytic Effect of Micellar Solution of Sodium Dodecyl Sulfate (SDS) for Regioselective Iodination of Aromatic Compounds with a Sodium Iodide/Cerium(IV) Trihydroxide Hydroperoxide System

Discovery of Allosteric and Selective Inhibitors of Inorganic Pyrophosphatase from Mycobacterium tuberculosis

Discovery and Optimization of Two Eis Inhibitor Families as Kanamycin Adjuvants against Drug-Resistant M. tuberculosis

Discovery and Optimization of 6‑(1-Substituted pyrrole-2-yl)‑s‑triazine Containing Compounds as Antibacterial Agents

Combating Enhanced Intracellular Survival (Eis)-Mediated Kanamycin Resistance of Mycobacterium tuberculosis by Novel Pyrrolo[1,5‑a]pyrazine-Based Eis Inhibitors

Structure-based design of haloperidol analogues as inhibitors of acetyltransferase Eis from to overcome kanamycin resistance

Potent 1,2,4-Triazino[5,6b]indole-3-thioether Inhibitors of the Kanamycin Resistance Enzyme Eis from Mycobacterium tuberculosis

A Minimalist NMR Approach for the Structural Revision of Mucoxin

Inside Cover: A Minimalist NMR Approach for the Structural Revision of Mucoxin (Chem. Eur. J. 46/2010)

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