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Lansoprazole a novel benzimidazole proton pump inhibitor and its related compounds have selective activity against Helicobacter pylori.

机译:兰索拉唑是一种新型苯并咪唑质子泵抑制剂其相关化合物对幽门螺杆菌具有选择性。

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摘要

The activities of various types of antiulcer agents against Helicobacter pylori (formerly called Campylobacter pylori) strains were determined by an agar dilution method. Among the compounds tested, two benzimidazole proton pump inhibitors, lansoprazole (AG-1749) and omeprazole, were found to have significant activities against this organism. The activity of lansoprazole was comparable to that of bismuth citrate, with MICs ranging from 3.13 to 12.5 micrograms/ml, and fourfold more potent than that of omeprazole. A major metabolite and two acid-converted rearrangement products of lansoprazole also exhibited good activities comparable or superior to that of the parent compound. Exposure to lansoprazole of H. pylori growing in a liquid medium led to an extensive loss of viability without a reduction in culture turbidity and produced an aberrant bacterial morphology characterized by the irregular constriction of cells and the collapse of cell surface structures. The antibacterial activity of lansoprazole and its related compounds was selective against H. pylori; common aerobic and anaerobic bacteria and Campylobacter jejuni were not inhibited by 100 micrograms/ml.
机译:通过琼脂稀释法测定各种类型的抗溃疡剂对幽门螺杆菌(以前称为幽门弯曲菌)的活性。在测试的化合物中,发现两种苯并咪唑质子泵抑制剂兰索拉唑(AG-1749)和奥美拉唑对这种生物具有显着活性。兰索拉唑的活性与柠檬酸铋相当,MIC范围为3.13至12.5微克/ ml,效力是奥美拉唑的四倍。兰索拉唑的主要代谢产物和两种酸转化的重排产物也表现出与母体化合物相当或更好的良好活性。暴露于在液体培养基中生长的幽门螺杆菌的兰索拉唑会导致活力的广泛丧失,而不会降低培养液的浊度,并且会产生异常的细菌形态,其特征在于细胞的不规则收缩和细胞表面结构的崩溃。兰索拉唑及其相关化合物的抗菌活性对幽门螺杆菌具有选择性。常见的需氧和厌氧细菌以及空肠弯曲菌的浓度均未受到100微克/毫升的抑制。

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