1,3,4-恶二唑和 1,2,4-三唑化合物对尿素酶和胃蛋白酶的影响

Zahraa M. Abdnoor, Nasreen R.Jber, Aliaa Saadoon Abdul-Razaq
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引用次数: 0

摘要

幽门螺旋杆菌会影响胃中的尿素酶和胃蛋白酶,因此本研究的目的是在体外筛选双 1,3,4-恶二唑和双 1,2,4,三唑衍生物化合物对幽门螺旋杆菌尿素酶的影响。结果表明,当浓度增加时,所有化合物都能抑制脲酶。最有效的脲酶抑制剂被确定为化合物(A3e、A3c、A3d 和 B3c)。临床研究包括研究幽门螺杆菌患者和对照组的胃蛋白酶活性水平,结果发现幽门螺杆菌患者的胃蛋白酶活性高于对照组。对所制备的化合物进行了胃蛋白酶体外筛选,结果表明,随着浓度的增加,所有制备的化合物都会降低胃蛋白酶的活性。含氮杂环化合物。本研究得出结论,含氮杂环化合物在治疗幽门螺旋杆菌疾病方面具有重要前景。
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The Effect of 1,3,4-Oxadiazol and 1,2,4-Triazole Compounds on Urease and Pepsin Enzymes
The helicobacter pylori affected urease and pepsin enzymes in the stomach, so the object of this study is to screen the effect of bis 1,3,4-oxadiazole and bis 1,2,4, triazole derivatives compounds on h-pylori urease enzyme in vitro. The results show that urease was inhibited by all produced compounds when the concentration increased. The most effective urease inhibitor is determined to be the compounds (A3e, A3c, A3d and B3c). The clinical study involved studying the pepsin enzyme activity level in H-pyloripatients and control, the results found that the activity of pepsin elevated in h-pylori patients as compared with control. The prepared compounds were screened on pepsin enzyme in vitro and showed that all the prepared compounds decreased the pepsin activity as the concentration increased. The nitrogen heterocyclic compounds. This study concludes that nitrogen-containing heterocyclic compounds have an important future in the treatment of Helicobacter pylori disease.
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