Issue 38, 2012

Remarkable in vitro bactericidal activity of bismuth(iii) sulfonates against Helicobacter pylori

Abstract

Four new tris-substituted bismuth(III) sulfonates of general formula [Bi(O3SR)3] (R = phenyl 1, p-tolyl 2, 2,4,6-mesityl 3 and S-(+)-10-camphoryl 4) have been synthesised and characterised. Their synthesis by solvent-free (SF) and solvent-mediated (SM) methods has been explored and their activity against Helicobacter pylori has been investigated. The compounds 1–4 display a remarkable in vitro activity against three laboratory strains of H. pylori (B128, 26 695 and 251) with minimum inhibitory concentration (MIC) values as low as 0.049 μg mL−1 for the strains B128 and 26 695, and 0.781 μg mL−1 for the clinical isolate 251. This places most MIC values in the nano-molar region and demonstrates the strong influence of the sulfonate group on the bactericidal properties. The novel solid state structure [Bi8(O3SMes)20(SO4)2(H2O)6]·(C7H8)75·(C777H888)777, derived from the SM reaction under reflux conditions, is presented and the incorporation of the two inorganic sulfate anions in the centre of the wheel-like bismuth sulfonate cluster explained.

Graphical abstract: Remarkable in vitro bactericidal activity of bismuth(iii) sulfonates against Helicobacter pylori

Supplementary files

Article information

Article type
Paper
Submitted
26 Jun 2012
Accepted
25 Jul 2012
First published
25 Jul 2012

Dalton Trans., 2012,41, 11798-11806

Remarkable in vitro bactericidal activity of bismuth(III) sulfonates against Helicobacter pylori

P. C. Andrews, M. Busse, G. B. Deacon, R. L. Ferrero, P. C. Junk, J. G. MacLellan and A. Vom, Dalton Trans., 2012, 41, 11798 DOI: 10.1039/C2DT31360J

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