中药对耐甲硝唑幽门螺杆菌对氧不敏感NADPH硝基还原酶的抑制作用

M. Saeed, A. Eghdami
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引用次数: 1

摘要

幽门螺杆菌是慢性胃炎、胃溃疡和胃癌的重要危险因素。本文的目的是研究从生姜和欧芹植物中提取的50种草药化合物对耐甲硝唑的幽门螺杆菌对氧不敏感的NADPH硝基还原酶的潜在影响。本研究分别从ZINC15、RCSB (Protein Data Bank)和PubChem等数据库中获取化合物的结构信息,以及对甲硝唑酶、肉豆蔻素和shogaol衍生物耐药的幽门螺杆菌。最后,使用iGemdock2.1和Molegro Virtual Docker进行分子对接。分子对接后,50个植物化合物中有4个与结合位点氨基酸的相互作用能量最低,相互作用次数最多。4种植物化合物中,以姜源n -香草烯酰胺效果最好。我们的分子对接研究表明,生姜可以作为抑制幽门螺杆菌生长的潜在候选物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibitory effect of herbal compounds on the Oxygen-insensitive NADPH nitro reductase enzyme of metronidazole-resistant Helicobacter pylori
Helicobacter pylori is a significant risk factor for chronic gastritis, gastric ulcers, and gastric cancer. The purpose of this article is to investigate the potential impact of fifty herbal compounds derived from Ginger and Parsley plants, known for their antibacterial properties on the Oxygen-insensitive NADPH nitro reductase enzyme of metronidazole-resistant H. pylori. In the present study, the information on the structure of compounds, the H. pylori resistant to metronidazole enzyme, myristicin, and shogaol derivatives were obtained from databases such as ZINC15, RCSB (Protein Data Bank), and PubChem, respectively. Finally, molecular docking was performed with iGemdock2.1 and Molegro Virtual Docker. After molecular docking, four out of the fifty phytocompounds showed the lowest energy and the highest number of interactions with the amino acids at the binding sites. Among these four phytocompounds, the best phytocompound was N-Vanillyloctanamide derived from Ginger. Our molecular docking study suggests that ginger can be introduced as a potential candidate to inhibit the growth of H. pylori.
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