1031431-96-5Relevant articles and documents
Fragment-to-hit-to-lead discovery of a novel pyridylurea scaffold of ATP competitive dual targeting type II topoisomerase inhibiting antibacterial agents
Basarab, Gregory S.,Manchester, John I.,Bist, Shanta,Boriack-Sjodin, P. Ann,Dangel, Brian,Illingworth, Ruth,Sherer, Brian A.,Sriram, Shubha,Uria-Nickelsen, Maria,Eakin, Ann E.
, p. 8712 - 8735 (2013/12/04)
The discovery and optimization of a new class of bacterial topoisomerase (DNA gyrase and topoisomerase IV) inhibitors binding in the ATP domain are described. A fragment molecule, 1-ethyl-3-(2-pyridyl)urea, provided sufficiently potent enzyme inhibition (
CHEMICAL COMPOUNDS
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Page/Page column 57, (2008/12/05)
Compounds of formula (I) and their pharmaceutically acceptable salts are described. Processes for their preparation, pharmaceutical compositions containing them, their use as medicaments and their use in the treatment of bacterial infections are also desc