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Baptiste Villemagne

Pasteur Institute

14

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320

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Rubrolone production by Dactylosporangium vinaceum: biosynthesis, modulation and possible biological function.

2021 Applied Microbiology and Biotechnology
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Fragment-based optimized EthR inhibitors with in vivo ethionamide boosting activity

2020 ACS Infectious Diseases
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Pyrrolomycins are Potent Natural Protonophores

2019 Antimicrobial Agents and Chemotherapy
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A fragment-based approach towards the discovery of N-substituted tropinones as inhibitors of Mycobacterium tuberculosis transcriptional regulator EthR2.

2019 European Journal of Medicinal Chemistry
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Recent advances in the design of inhibitors of mycobacterial transcriptional regulators to boost thioamides anti-tubercular activity and circumvent acquired-resistance

2019 Annual Reports in Medicinal Chemistry
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Unconventional surface plasmon resonance signals reveal quantitative inhibition of transcriptional repressor EthR by synthetic ligands.

2014 Analytical Biochemistry
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Ligand Efficiency Driven Design of New Inhibitors of Mycobacterium tuberculosis Transcriptional Repressor EthR Using Fragment Growing, Merging, and Linking Approaches.

2014 Journal of Medicinal Chemistry
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Tuberculosis: The Drug Developemnt Pipeline at a Glance

2012 ChemInform
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Ethionamide Boosters. 2. Combining Bioisosteric Replacement and Structure-Based Drug Design To Solve Pharmacokinetic Issues in a Series of Potent 1,2,4-Oxadiazole EthR Inhibitors

2011 Journal of Medicinal Chemistry
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Citations (56)