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pubmed-article:17923406pubmed:abstractTextA new small molecule inhibitor of bacterial cell division has been discovered using a high-throughput screen in Escherichia coli. Although the lead screening hit (534F6) exhibited modest inhibition of the GTPase activity of FtsZ (20+/-5% at 100microM of compound), a primary target for bacterial cell division inhibitors, several analogs caused potent bacterial growth inhibition with negligible antagonism of FtsZ GTPase activity. A library of analogs has been prepared and several alkyne-tagged photoaffinity probes have been synthesized for use in experiments to elucidate the primary target of this compound.lld:pubmed
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pubmed-article:17923406pubmed:articleTitleN-Benzyl-3-sulfonamidopyrrolidines as novel inhibitors of cell division in E. coli.lld:pubmed
pubmed-article:17923406pubmed:affiliationBroad Institute of Harvard and MIT, 7 Cambridge Center, Cambridge, MA 02142, USA.lld:pubmed
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