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CAS No. : 80621-81-4
MCE 国际站:Rifaximin
产品活性:Rifaximin是一种胃肠道选择性的抗生素 (antibiotic),与细菌 DNA 依赖性 RNA 聚合酶的 β 亚基结合,从而抑制细菌 RNA 的合成 (bacterial RNA synthesis)。与革兰氏阴性菌(MIC:8-50 毫克/毫升)相比,Rifaximin对革兰氏阳性菌株(MIC:0.03-5 毫克/毫升)的敏感性更高。
研究领域:Anti-infection | Cell Cycle/DNA Damage
作用靶点:Bacterial | Antibiotic | DNA/RNA Synthesis
In Vitro: Rifaximin has a good inhibitory activity against Staphylococcus, Streptococcus, Enterococcus, Escherichia coli, Shigella, Salmonella, Bacillus cereus, Moraxella catarrhalis, Haemophilus influenzae, Haemophilus ducreyi, Bacteroides bivius-disiens, Gardnerella vaginalis, Lactobacillus spp.,Mobiluncus spp.,Neisseria gonorrhoeae, Pseudomonas and Acinetobacter . Rifaximin rarely causes side effects.
Rifaximin (0.1, 1.0 and 10.0 µM) causes significant and concentration-dependent reduction of cell proliferation, cell migration and PCNA expression in the Caco-2 cells vs. untreated cells.
Rifaximin (0.1-10 μM) downregulates Akt/mTOR and p38MAPK/NF-κB pathways through a PXR-dependent mechanism.
In Vivo: Rifaximin administration (30 or 50 mg/kg/day) increases survival rates of colitic mice and reduces colitis severity by improvement of wasting syndrome, histologic scores, decrease in colon IL-2, IL-12, IFN-gamma and TNF-alpha (protein and mRNA) levels, and diminishes colon myeloperoxidase (MPO) activity.
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