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Privileged Scaffolds or Promiscuous Binders: A Comparative Study on Rhodanines and Related Heterocycles in Medicinal Chemistry

Journal of medicinal chemistry, 2012-01, Vol.55 (2), p.743-753

2012

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Biochemistry and Medicinal Chemistry of the Dengue Virus Protease

Chemical reviews, 2014-11, Vol.114 (22), p.11348-11381

2014

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Promiscuity and Selectivity in Covalent Enzyme Inhibition: A Systematic Study of Electrophilic Fragments

Journal of medicinal chemistry, 2014-09, Vol.57 (18), p.7590-7599

2014

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Virtues of Volatility: A Facile Transesterification Approach to Boronic Acids

Organic letters, 2019-05, Vol.21 (9), p.3048-3052

2019

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Peptide–Boronic Acid Inhibitors of Flaviviral Proteases: Medicinal Chemistry and Structural Biology

Journal of medicinal chemistry, 2017-01, Vol.60 (1), p.511-516

2017

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Discovery of Nanomolar Dengue and West Nile Virus Protease Inhibitors Containing a 4‑Benzyloxyphenylglycine Residue

Journal of medicinal chemistry, 2015-12, Vol.58 (23), p.9354-9370

2015

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Sensitive NMR Approach for Determining the Binding Mode of Tightly Binding Ligand Molecules to Protein Targets

Journal of the American Chemical Society, 2016-04, Vol.138 (13), p.4539-4546

2016

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Diversity-oriented synthesis of peptide-boronic acids by a versatile building-block approach

Chemical science (Cambridge), 2020-08, Vol.11 (36), p.9898-993

2020

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Identification of fused bicyclic derivatives of pyrrolidine and imidazolidinone as dengue virus-2 NS2B-NS3 protease inhibitors

European journal of medicinal chemistry, 2017-01, Vol.125, p.751-759

2017

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De Novo Discovery of Nonstandard Macrocyclic Peptides as Noncompetitive Inhibitors of the Zika Virus NS2B-NS3 Protease

ACS medicinal chemistry letters, 2019-02, Vol.10 (2), p.168-174

2019

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Crystal structure of Zika virus NS2B-NS3 protease in complex with a boronate inhibitor

Science (American Association for the Advancement of Science), 2016-07, Vol.353 (6298), p.503-505

2016

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Backbone modifications in peptidic inhibitors of flaviviral proteases

Bioorganic & medicinal chemistry letters, 2019-08, Vol.29 (15), p.1913-1917

2019

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Metal-Mediated Inhibition of Escherichia coli Methionine Aminopeptidase: Structure−Activity Relationships and Development of a Novel Scoring Function for Metal−Ligand Interactions

Journal of medicinal chemistry, 2006-01, Vol.49 (2), p.511-522

2006

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Broad-spectrum agents for flaviviral infections: dengue, Zika and beyond

Nature reviews. Drug discovery, 2017-08, Vol.16 (8), p.565-586

2017

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Structure–activity relationships of tulipalines, tuliposides, and related compounds as inhibitors of MurA

Bioorganic & medicinal chemistry letters, 2010-10, Vol.20 (19), p.5757-5762

2010

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C‑Terminal Residue Optimization and Fragment Merging: Discovery of a Potent Peptide-Hybrid Inhibitor of Dengue Protease

ACS medicinal chemistry letters, 2014-09, Vol.5 (9), p.1037-1042

2014

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Arylcyanoacrylamides as inhibitors of the Dengue and West Nile virus proteases

Bioorganic & medicinal chemistry, 2011-12, Vol.19 (24), p.7318-7337

2011

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N-sulfonyl peptide-hybrids as a new class of dengue virus protease inhibitors

European journal of medicinal chemistry, 2023-05, Vol.251, p.115227-115227, Article 115227

2023

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Inhibitor potency and assay conditions: A case study on SARS-CoV-2 main protease

Proceedings of the National Academy of Sciences - PNAS, 2021-09, Vol.118 (36)

2021

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The Medicinal Chemistry of Dengue Virus

Journal of medicinal chemistry, 2016-06, Vol.59 (12), p.5622-5649

2016

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Machine Learning in Mass Spectrometry: A MALDI-TOF MS Approach to Phenotypic Antibacterial Screening

Journal of medicinal chemistry, 2020-08, Vol.63 (16), p.8849-8856

2020

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Phenylalanine and Phenylglycine Analogues as Arginine Mimetics in Dengue Protease Inhibitors

Journal of medicinal chemistry, 2015-10, Vol.58 (19), p.7719-7733

2015

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Discovery of potent benzoxaborole inhibitors against SARS-CoV-2 main and dengue virus proteases

European journal of medicinal chemistry, 2022-10, Vol.240, p.114585-114585, Article 114585

2022

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2,2′-Bithiophene as sensor tag for ligand–protein binding assays based on Förster resonance energy transfer

Analytical biochemistry, 2023-12, Vol.682, p.115335-115335, Article 115335

2023

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The Unusual Binding Mode of Cnicin to the Antibacterial Target Enzyme MurA Revealed by X-ray Crystallography

Journal of medicinal chemistry, 2008-08, Vol.51 (16), p.5143-5147

2008

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Privileged Scaffolds or Promiscuous Binders: A Comparative Study on Rhodanines and Related Heterocycles in Medicinal Chemistry

Biochemistry and Medicinal Chemistry of the Dengue Virus Protease

Promiscuity and Selectivity in Covalent Enzyme Inhibition: A Systematic Study of Electrophilic Fragments

Virtues of Volatility: A Facile Transesterification Approach to Boronic Acids

Peptide–Boronic Acid Inhibitors of Flaviviral Proteases: Medicinal Chemistry and Structural Biology

Discovery of Nanomolar Dengue and West Nile Virus Protease Inhibitors Containing a 4‑Benzyloxyphenylglycine Residue

Sensitive NMR Approach for Determining the Binding Mode of Tightly Binding Ligand Molecules to Protein Targets

Diversity-oriented synthesis of peptide-boronic acids by a versatile building-block approach

Identification of fused bicyclic derivatives of pyrrolidine and imidazolidinone as dengue virus-2 NS2B-NS3 protease inhibitors

De Novo Discovery of Nonstandard Macrocyclic Peptides as Noncompetitive Inhibitors of the Zika Virus NS2B-NS3 Protease

Crystal structure of Zika virus NS2B-NS3 protease in complex with a boronate inhibitor

Backbone modifications in peptidic inhibitors of flaviviral proteases

Metal-Mediated Inhibition of Escherichia coli Methionine Aminopeptidase: Structure−Activity Relationships and Development of a Novel Scoring Function for Metal−Ligand Interactions

Broad-spectrum agents for flaviviral infections: dengue, Zika and beyond

Structure–activity relationships of tulipalines, tuliposides, and related compounds as inhibitors of MurA

C‑Terminal Residue Optimization and Fragment Merging: Discovery of a Potent Peptide-Hybrid Inhibitor of Dengue Protease

Arylcyanoacrylamides as inhibitors of the Dengue and West Nile virus proteases

N-sulfonyl peptide-hybrids as a new class of dengue virus protease inhibitors

Inhibitor potency and assay conditions: A case study on SARS-CoV-2 main protease

The Medicinal Chemistry of Dengue Virus

Machine Learning in Mass Spectrometry: A MALDI-TOF MS Approach to Phenotypic Antibacterial Screening

Phenylalanine and Phenylglycine Analogues as Arginine Mimetics in Dengue Protease Inhibitors

Discovery of potent benzoxaborole inhibitors against SARS-CoV-2 main and dengue virus proteases

2,2′-Bithiophene as sensor tag for ligand–protein binding assays based on Förster resonance energy transfer

The Unusual Binding Mode of Cnicin to the Antibacterial Target Enzyme MurA Revealed by X-ray Crystallography

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