Hélène Munier-Lehmann

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Institut Pasteur

France

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Inserm permanent position

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Articles (15)

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2025

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2024

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2024

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2024

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2023

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2023

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2023

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2023

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2023

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2022

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2022

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2021

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2021

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2020

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2020

Collaborators (12)

Timothy P. O’Sullivan

University College Cork

IRELAND

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Sylvain Baize

INSERM

FRANCE

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Jana Sopkova-de Oliveira Santos

Université de Caen Normandie

FRANCE

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Anne Brelot

INSERM

FRANCE

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Bertrand raynal

Institut Pasteur

FRANCE

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Brigitte Gicquel

Professor

Institut Pasteur

FRANCE

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Marcelo Guerin

Professor

SPAIN

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Noelia Alonso-Rodríguez

University of Oslo

NORWAY

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Lionel Guittat

LOB - Laboratoire d’Optique et Biosciences CNRS UMR7645 – INSERM U1182

FRANCE

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Quentin Giai Gianetto

Institut Pasteur

FRANCE

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Patrick Bron

University of Montpellier

FRANCE

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ANASTASSIA KOMAROVA

Université Paris Cité

FRANCE

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Hélène Munier-Lehmann

Research Interests

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Recent Grants

Articles (15)

Design, synthesis, biophysical and biological evaluation of original condensed pyrrolopyrimidine and pyrrolopyridine ligands as anti-SARS-CoV-2 agents targeting G4

Synthesis, evaluation and mechanistic insights of novel IMPDH inhibitors targeting ESKAPEE bacteria

An equine iPSC-based phenotypic screening platform identifies pro- and anti-viral molecules against West Nile virus

A journey into the regulatory secrets of the de novo purine nucleotide biosynthesis

Insight into the role of the Bateman domain at the molecular and physiological levels through engineered IMP dehydrogenases

Interaction network among de novo purine nucleotide biosynthesis enzymes in Escherichia coli

SigH stress response mediates killing of <i>Mycobacterium tuberculosis</i> by activating nitronaphthofuran prodrugs via induction of Mrx2 expression

Discovery of Bis-Imidazoline Derivatives as New CXCR4 Ligands

Novel Antiviral Molecules against Ebola Virus Infection

Steroid hormone catabolites activate the pyrin inflammasome through a non-canonical mechanism

Structural basis for the allosteric inhibition of UMP kinase from Gram‐positive bacteria, a promising antibacterial target

Structure-aided optimization of non-nucleoside M. tuberculosis thymidylate kinase inhibitors

SARS-CoV-2 Nsp3 unique domain SUD interacts with guanine quadruplexes and G4-ligands inhibit this interaction

2-((3,5-Dinitrobenzyl)thio)quinazolinones: Potent Antimycobacterial Agents Activated by Deazaflavin (F<sub>420</sub>)-Dependent Nitroreductase (Ddn).

Endeavors towards transformation of M. tuberculosis thymidylate kinase (MtbTMPK) inhibitors into potential antimycobacterial agents

Collaborators (12)

Timothy P. O’Sullivan

Sylvain Baize

Jana Sopkova-de Oliveira Santos

Anne Brelot

Bertrand raynal

Brigitte Gicquel

Marcelo Guerin

Noelia Alonso-Rodríguez

Lionel Guittat

Quentin Giai Gianetto

Patrick Bron

ANASTASSIA KOMAROVA

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