| Literature DB >> 21684746 |
Wei-Chu Xu1, George E Wright, Neal C Brown, Zheng-Yu Long, Cheng-Xin Zhi, Sofya Dvoskin, Joseph J Gambino, Marjorie H Barnes, Michelle M Butler.
Abstract
Several 2-anilino- and 2-benzylamino-3-deaza-6-oxopurines [3-deazaguanines] and selected 8-methyl and 8-aza analogs have been synthesized. 7-Substituted N(2)-(3-ethyl-4-methylphenyl)-3-deazaguanines were potent and selective inhibitors of Gram+ bacterial DNA polymerase (pol) IIIC, and 7-substituted N(2)-(3,4-dichlorobenzyl)-3-deazaguanines were potent inhibitors of both pol IIIC and pol IIIE from Gram+ bacteria, but weakly inhibited pol IIIE from Gram- bacteria. Potent enzyme inhibitors in both classes inhibited the growth of Gram+ bacteria (MICs 2.5-10μg/ml), and were inactive against the Gram- organism Escherichia coli. Several derivatives had moderate protective activity in Staphylococcus aureus-infected mice.Entities:
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Year: 2011 PMID: 21684746 PMCID: PMC3128661 DOI: 10.1016/j.bmcl.2011.05.093
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823