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In Silico Evaluation for the Inhibitory Action of Curcumin Derivatives on the SARS-CoV-2 Proteins
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作者 Areej Jaradat Yasmeen Salameh +1 位作者 Hilal Zaid Siba Shanak 《Journal of Biosciences and Medicines》 2022年第4期63-76,共14页
Purpose of the Study: COVID-19 is caused by the SARS-CoV-2 virus that had a global pandemic spread in the last two years. Symptoms of the disease include respiratory distress and, in severe cases may consequently lead... Purpose of the Study: COVID-19 is caused by the SARS-CoV-2 virus that had a global pandemic spread in the last two years. Symptoms of the disease include respiratory distress and, in severe cases may consequently lead to death. Blocking the viral proteins can aid in treating this disease and alleviating its symptoms. Two target proteins of the coronavirus that are hot spots in drug discovery are the papain-like protease PL-pro and the main protease M-pro. PL-pro is an enzyme that is required for processing viral polyproteins to generate a functional replicase complex and enable viral spread. M-pro is the major protease of SARS-CoV-2, which is a keystone in viral replication and transcription. Methods: In this study, we shed the light on the route of targeting viral proteins for disease alleviation, by targeting the two aforementioned enzymes, PL-pro and M-pro using in silico studies. Docking experiments, using AutoDock algorithms, were performed to predict the inhibitory effect of recently produced synthetic derivatives of curcumin on the viral proteins. Results: Most of the curcumin derivatives have shown variable levels of inhibition, e.g., S1 - S6, mainly on the papain-like protease, and to a lesser extent on the main protease. Conclusion: The results indicated that curcumin derivatives can be potent anti-viral drug of SARS-CoV-2, namely targeting the papain-like protease. 展开更多
关键词 Natural Compounds Curcumin Derivatives In Silico DOCKING SARS-CoV-2 COVID-19 PHYTOCHEMICALS pl-pro M-Pro CORONAVIRUS
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靶向SARS-CoV-2 PL^(pro)抑制剂的研究进展
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作者 高雨 张国宁 王玉成 《中国药学杂志》 CSCD 北大核心 2024年第23期2205-2215,共11页
2019年末,新型冠状病毒(SARS-CoV-2),即严重急性呼吸系统综合征冠状病毒2席卷全球,对社会经济和人类健康造成了不可逆转的危害,相应的抗病毒药物研发也因此受到了广泛关注。SARS-CoV-2主要通过飞沫传播,并在宿主细胞内经历复制、转录与... 2019年末,新型冠状病毒(SARS-CoV-2),即严重急性呼吸系统综合征冠状病毒2席卷全球,对社会经济和人类健康造成了不可逆转的危害,相应的抗病毒药物研发也因此受到了广泛关注。SARS-CoV-2主要通过飞沫传播,并在宿主细胞内经历复制、转录与翻译过程后,以胞吞形式排出成熟病毒,构成感染闭环。值得注意的是,非结构蛋白3(nsp3)编码的木瓜蛋白酶样蛋白酶(PL^(pro))在这个过程中发挥着重要作用。同时在去泛素化等炎症反应中,PL^(pro)也会帮助病毒逃避相应的免疫反应。因此,靶向抑制PL^(pro),不仅能够阻断病毒整体的复制过程,也可以恢复宿主自身的免疫功能,从而达到更好的抗SARS-CoV-2效果。综上,本文拟从化合物的不同结构出发,对近年来靶向SARS-CoV-2 PL^(pro)的抑制剂研究进行探索性总结,以期为抗SARS-CoV-2的药物发现提供理论参考。 展开更多
关键词 新型冠状病毒 木瓜蛋白酶样蛋白酶靶点 抑制剂 治疗药物
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在SQL^*FORM程序中使用用户口令
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作者 胡南相 《计算机工程》 EI CAS CSCD 北大核心 1997年第5期64-65,共2页
该文介绍在SQLFORM程序中如何得到用户注册口令,以便实现灵活的系统维护和用户管理,并给出一个应用实例.
关键词 数据库 用户口令 SQL*FORM程序
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