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• W2171091607 abstract "The mechanochemical synthesis and characterization of a zinc complex with famotidine is described. The complex was characterized by microanalysis and a number of spectroscopic techniques. The complex was of M:L dihydrate type. Derivatization of famotidine with zinc appears to enhance the activity of the drug by inhibiting the growth of Helicobacter pylori (two reference and 34 clinical isolates). The complex inhibited the growth of H. pylori in an MIC range of 1-8 microg mL(-1). The anti-H. pylori activity of the zinc-famotidine complex against antibiotic-resistant strains was nearly comparable to that of antibiotic-susceptible strains. The complex was found to be far less toxic than the parent drug, as demonstrated by its higher LD(50) value. In the human urease enzyme inhibition assay the complex exhibited significant inhibition. The new complex appears to be more useful in eradicating both the antibiotic-susceptible and antibiotic-resistant strains of H. pylori." @default.
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• W2171091607 date "2009-10-26" @default.
• W2171091607 modified "2023-10-14" @default.
• W2171091607 title "Mechanochemical synthesis and<i>in vitro</i>anti-<i>Helicobacter pylori</i>and uresase inhibitory activities of novel zinc(II)–famotidine complex" @default.
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• W2171091607 doi "https://doi.org/10.3109/14756360903179518" @default.
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