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基于分子对接,分子动力学和结合自由能的新型潜在的尼帕病毒多目标抑制剂的识别

Prashasti Sinha1, Anil Kumar Yadav1

  • 1Department of Physics, School of Physical & Decision Science, Babasaheb Bhimrao Ambedkar University, Lucknow, Uttar Pradesh, India.

Journal of biomolecular structure & dynamics
|November 3, 2023
PubMed
概括

研究人员设计了针对尼帕病毒 (NiV) 感染的新型多目标抑制剂. 五种化合物显示出有前途的类似药物的特性和强大的结合亲和力,表明这种严重的神经疾病的潜在新抗病毒治疗方法.

关键词:
在MM/PBSA分析中,尼帕病毒是尼帕病毒.分子对接的分子对接.分子动力学分子动力学多目标多目标.

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