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Arabian journal of chemistry. 2023 Sep;16(9):105051. doi: 10.1016/j.arabjc.2023.105051

A suitable drug structure for interaction with SARS-CoV-2 main protease between boceprevir, masitinib and rupintrivir; a molecular dynamics study

针对SARS-CoV-2主要蛋白酶的博赛普韦、马西替坦和芦帕曲辛相互作用的适宜药物结构——分子动力学研究 翻译改进

Mehdi Yoosefian  1  2, Razieh Dashti  2, Mohamad Mahani  1, Leila Montazer  1, Amirabbas Mir  3

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作者单位

  • 1 Department of Chemistry, Graduate University of Advanced Technology, Kerman, Iran.
  • 2 Department of Nanotechnology, Graduate University of Advanced Technology, Kerman, Iran.
  • 3 Institute of Nano Science and Nano Technology, University of Kashan, Kashan P.O. Box 87317-51167, Iran.
  • DOI: 10.1016/j.arabjc.2023.105051 PMID: 37323221

    摘要 Ai翻译

    In recent years, more than 200 countries of the world have faced a health crisis due to the epidemiological disease of COVID-19 caused by the SARS-CoV-2 virus. It had a huge impact on the world economy and the global health sector. Researchers are studying the design and discovery of drugs that can inhibit SARS-CoV-2. The main protease of SARS-CoV-2 is an attractive target for the study of antiviral drugs against coronavirus diseases. According to the docking results, binding energy for boceprevir, masitinib and rupintrivir with CMP are -10.80, -9.39, and -9.51 kcal/mol respectively. Also, for all investigated systems, van der Waals and electrostatic interactions are quite favorable for binding the drugs to SARS-CoV-2 coronavirus main protease, indicating confirmation of the complex stability.

    Keywords: Boceprevir; Masitinib; Protease inhibitor; Rupintrivir; SARS‐CoV‐2 main protease.

    Keywords:drug structure; sars-cov-2 main protease; molecular dynamics study

    Copyright © Arabian journal of chemistry. 中文内容为AI机器翻译,仅供参考!

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    A suitable drug structure for interaction with SARS-CoV-2 main protease between boceprevir, masitinib and rupintrivir; a molecular dynamics study