EXPERIMENTAL DRUGS / POTENTIAL ANTIBIOTIC THERAPIES AGAINST M. ULCERANS
Moxifloxacin, R207910 and linezolid
TARGET PROTEIN
topoisomerase II (DNA gyrase) and topoisomerase IV
MECHANISM OF ACTION
Bactericidal activity
DRUG INTERACTION PHASE (APPROVED, INVESTIGATIONAL, EXPERIMENTAL)
Experimental
MODE OF ADMINISTRATION
Oral
LINK TO PUBMED
https://pubmed.ncbi.nlm.nih.gov/16723546/
EXTERNAL LINKS
PubChem Compound 152946
REFERENCE
Ji, B., Lefrancois, S., Robert, J., Chauffour, A., Truffot, C., & Jarlier, V. (2006). In vitro and in vivo activities of rifampin, streptomycin, amikacin, moxifloxacin, R207910, linezolid, and PA-824 against Mycobacterium ulcerans. Antimicrobial Agents and Chemotherapy, 50(6), 1921?1926. https://doi.org/10.1128/AAC.00052-06 Kim, H., Mori, S., Kenri, T., & Suzuki, Y. (2021). Molecular characterization of Mycobacterium ulcerans DNA gyrase and identification of mutations reduced susceptibility against quinolones in vitro. BioRxiv, 2021.09.29.462499. https://doi.org/10.1101/2021.09.29.462499 Organization, W. H. (2012). Treatment of Mycobacterium ulcerans disease (Buruli Ulcer): Guidance for health workers. | Infolep. https://www.leprosy-information.org/resource/treatment-mycobacterium-ulcerans-disease-buruli-ulcer-guidance-health-workers