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Diarylquinolines target subunit c of mycobacterial ATP synthase.

Nature chemical biology (2007-05-15)
Anil Koul, Najoua Dendouga, Karen Vergauwen, Brenda Molenberghs, Luc Vranckx, Rudy Willebrords, Zorica Ristic, Holger Lill, Ismet Dorange, Jerome Guillemont, Dirk Bald, Koen Andries
RESUMEN

The diarylquinoline R207910 (TMC207) is a promising candidate in clinical development for the treatment of tuberculosis. Though R207910-resistant mycobacteria bear mutations in ATP synthase, the compound's precise target is not known. Here we establish by genetic, biochemical and binding assays that the oligomeric subunit c (AtpE) of ATP synthase is the target of R207910. Thus targeting energy metabolism is a new, promising approach for antibacterial drug discovery.

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Sigma-Aldrich
TMC207, ≥98% (HPLC)
Sigma-Aldrich
Rifampicina, ≥95% (HPLC), powder or crystals
Sigma-Aldrich
Rifampicina, suitable for plant cell culture, BioReagent, ≥95% (HPLC), powder or crystals