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QM/MM Calculations Reveal the Different Nature of the Interaction of Two Carborane-Based Sulfamide Inhibitors of Human Carbonic Anhydrase II

The journal of physical chemistry. B, 2013-12, Vol.117 (50), p.16096-16104

2013

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Inhibitors of CA IX Enzyme Based on Polyhedral Boron Compounds

Chembiochem : a European journal of chemical biology, 2021-09, Vol.22 (18), p.2741-2761

2021

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Validation and structural characterization of the LEDGF/p75-MLL interface as a new target for the treatment of MLL-dependent leukemia

Cancer research (Chicago, Ill.), 2014-09, Vol.74 (18), p.5139-5151

2014

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Structure-Aided Design of Novel Inhibitors of HIV Protease Based on a Benzodiazepine Scaffold

Journal of medicinal chemistry, 2012-11, Vol.55 (22), p.10130-10135

2012

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Affinity switching of the LEDGF/p75 IBD interactome is governed by kinase-dependent phosphorylation

Proceedings of the National Academy of Sciences - PNAS, 2018-07, Vol.115 (30), p.E7053-E7062

2018

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Multiple cellular proteins interact with LEDGF/p75 through a conserved unstructured consensus motif

Nature communications, 2015-08, Vol.6 (1), p.7968-7968, Article 7968

2015

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Carborane-Based Carbonic Anhydrase Inhibitors

Angewandte Chemie International Edition, 2013-12, Vol.52 (51), p.13760-13763

International ed. in English, 2013

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A tick salivary protein targets cathepsin G and chymase and inhibits host inflammation and platelet aggregation

Blood, 2011-01, Vol.117 (2), p.736-744

2011

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Imidazo[1,2-c]pyrimidin-5(6H)-one inhibitors of CDK2: Synthesis, kinase inhibition and co-crystal structure

European journal of medicinal chemistry, 2021-04, Vol.216, p.113309-113309, Article 113309

2021

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Direct Introduction of an Alkylsulfonamido Group on C‐sites of Isomeric Dicarba‐closo‐dodecaboranes: The Influence of Stereochemistry on Inhibitory Activity against the Cancer‐Associated Carbonic Anhydrase IX Isoenzyme

Chemistry : a European journal, 2020-12, Vol.26 (69), p.16541-16553

2020

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Triggering HIV polyprotein processing by light using rapid photodegradation of a tight-binding protease inhibitor

Nature communications, 2015-03, Vol.6 (1), p.6461-6461, Article 6461

2015

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Molecular Characterization of Clinical Isolates of Human Immunodeficiency Virus Resistant to the Protease Inhibitor Darunavir

Journal of Virology, 2009-09, Vol.83 (17), p.8810-8818

2009

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Sulfonamido carboranes as highly selective inhibitors of cancer-specific carbonic anhydrase IX

European journal of medicinal chemistry, 2020-08, Vol.200, p.112460, Article 112460

2020

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DNA-linked inhibitor antibody assay (DIANA) as a new method for screening influenza neuraminidase inhibitors

Biochemical journal, 2018-12, Vol.475 (23), p.3847-3860

2018

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The structural basis for the selectivity of sulfonamido dicarbaboranes toward cancer-associated carbonic anhydrase IX

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.1800-1810

2020

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Mutations in HIV-1 gag and pol Compensate for the Loss of Viral Fitness Caused by a Highly Mutated Protease

Antimicrobial Agents and Chemotherapy, 2012-08, Vol.56 (8), p.4320-4330

2012

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Synthesis, Structure–Activity Relationship Studies, and X-ray Crystallographic Analysis of Arylsulfonamides as Potent Carbonic Anhydrase Inhibitors

Journal of medicinal chemistry, 2012-04, Vol.55 (8), p.3891-3899

2012

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Kinetic, Thermodynamic, and Structural Analysis of Drug Resistance Mutations in Neuraminidase from the 2009 Pandemic Influenza Virus

Viruses, 2018-06, Vol.10 (7), p.339

2018

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Carbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms

European journal of medicinal chemistry, 2015-09, Vol.102, p.223-232

2015

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Structural Basis for Inhibition of Cathepsin B Drug Target from the Human Blood Fluke, Schistosoma mansoni

The Journal of biological chemistry, 2011-10, Vol.286 (41), p.35770-35781

2011

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Structural Basis for the Interaction Between Carbonic Anhydrase and 1,2,3,4-tetrahydroisoquinolin-2-ylsulfonamides

Journal of medicinal chemistry, 2011-04, Vol.54 (7), p.2522-2526

2011

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Feasibility and constraints of particle targeting using the antigen-antibody interaction

Nanoscale, 2013-12, Vol.5 (23), p.11490-11498

2013

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Ninety-Nine Is Not Enough: Molecular Characterization of Inhibitor-Resistant Human Immunodeficiency Virus Type 1 Protease Mutants with Insertions in the Flap Region

Journal of Virology, 2008-06, Vol.82 (12), p.5869-5878

2008

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Oligomeric interface modulation causes misregulation of purine 5´-nucleotidase in relapsed leukemia

BMC biology, 2016-10, Vol.14 (1), p.91-91, Article 91

2016

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Kinetic, thermodynamic and structural analysis of tamiphosphor binding to neuraminidase of H1N1 (2009) pandemic influenza

European journal of medicinal chemistry, 2016-10, Vol.121, p.100-109

2016

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QM/MM Calculations Reveal the Different Nature of the Interaction of Two Carborane-Based Sulfamide Inhibitors of Human Carbonic Anhydrase II

Inhibitors of CA IX Enzyme Based on Polyhedral Boron Compounds

Validation and structural characterization of the LEDGF/p75-MLL interface as a new target for the treatment of MLL-dependent leukemia

Structure-Aided Design of Novel Inhibitors of HIV Protease Based on a Benzodiazepine Scaffold

Affinity switching of the LEDGF/p75 IBD interactome is governed by kinase-dependent phosphorylation

Multiple cellular proteins interact with LEDGF/p75 through a conserved unstructured consensus motif

Carborane-Based Carbonic Anhydrase Inhibitors

A tick salivary protein targets cathepsin G and chymase and inhibits host inflammation and platelet aggregation

Imidazo[1,2-c]pyrimidin-5(6H)-one inhibitors of CDK2: Synthesis, kinase inhibition and co-crystal structure

Direct Introduction of an Alkylsulfonamido Group on C‐sites of Isomeric Dicarba‐closo‐dodecaboranes: The Influence of Stereochemistry on Inhibitory Activity against the Cancer‐Associated Carbonic Anhydrase IX Isoenzyme

Triggering HIV polyprotein processing by light using rapid photodegradation of a tight-binding protease inhibitor

Molecular Characterization of Clinical Isolates of Human Immunodeficiency Virus Resistant to the Protease Inhibitor Darunavir

Sulfonamido carboranes as highly selective inhibitors of cancer-specific carbonic anhydrase IX

DNA-linked inhibitor antibody assay (DIANA) as a new method for screening influenza neuraminidase inhibitors

The structural basis for the selectivity of sulfonamido dicarbaboranes toward cancer-associated carbonic anhydrase IX

Mutations in HIV-1 gag and pol Compensate for the Loss of Viral Fitness Caused by a Highly Mutated Protease

Synthesis, Structure–Activity Relationship Studies, and X-ray Crystallographic Analysis of Arylsulfonamides as Potent Carbonic Anhydrase Inhibitors

Kinetic, Thermodynamic, and Structural Analysis of Drug Resistance Mutations in Neuraminidase from the 2009 Pandemic Influenza Virus

Carbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms

Structural Basis for Inhibition of Cathepsin B Drug Target from the Human Blood Fluke, Schistosoma mansoni

Structural Basis for the Interaction Between Carbonic Anhydrase and 1,2,3,4-tetrahydroisoquinolin-2-ylsulfonamides

Feasibility and constraints of particle targeting using the antigen-antibody interaction

Ninety-Nine Is Not Enough: Molecular Characterization of Inhibitor-Resistant Human Immunodeficiency Virus Type 1 Protease Mutants with Insertions in the Flap Region

Oligomeric interface modulation causes misregulation of purine 5´-nucleotidase in relapsed leukemia

Kinetic, thermodynamic and structural analysis of tamiphosphor binding to neuraminidase of H1N1 (2009) pandemic influenza

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