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

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Villemagne, Baptiste | Flipo, Marion | Blondiaux, Nicolas | Crauste, Celine | Malaquin, Sandra | Leroux, Florence | Piveteau, Catherine | Villeret, Vincent | Brodin, Priscille | Villoutreix, Bruno, O. | Sperandio, Olivier | Soror, Sameh, H. | Wohlkönig, Alexandre | Wintjens, René | Deprez, Benoit | Baulard, Alain, R. | Willand, Nicolas

Edité par CCSD ; American Chemical Society -

International audience. Tuberculosis remains a major cause of mortality and morbidity, killing each year more than one million people. Although the combined use of first line antibiotics (isoniazid, rifampicin, pyrazinamide and ethambutol) is efficient to treat most patients, the rapid emergence of multidrug resistant strains of Mycobacterium tuberculosis stresses the need for alternative therapies. Mycobacterial transcriptional repressor EthR is a key player in the control of second-line drugs bioactivation such as ethionamide, and has been shown to impair the sensitivity of the human pathogen Mycobacterium tuberculosis to this antibiotic. As a way to identify new potent ligands of this protein we have developed fragment-based approaches. In the current study we combined surface plasmon resonance assay, X-ray crystallography, ligand efficiency driven design for the rapid discovery and optimization of new chemotypes of EthR ligands starting from a fragment. The design, synthesis, in vitro and ex vivo activities of these compounds will be discussed.

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