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Updated: Jun 29, 2026

Development of Inhibitors of Protein-protein Interactions through REPLACE: Application to the Design and Development Non-ATP Competitive CDK Inhibitors
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设计新型伊米达衍生物作为潜在的非核酸逆转录酶抑制剂,使用分子对接和动力学策略

Priyanka Chandra1, Swastika Ganguly1, Pran Kishore Deb1

  • 1Department of Pharmaceutical Sciences and Technology, Birla Institute of Technology, Mesra, Ranchi, Jharkhand PIN-835215, India.

Current pharmaceutical design
|October 2, 2024
PubMed
概括

研究人员设计了新的伊米达化合物来抑制HIV-1-RT,这是抗逆转录病毒治疗向的酶. 伊米达衍生物SP08在开发抗药性HIV病毒株的新疗法方面表现最有前途.

关键词:
我们承认.艾滋病 艾滋病 艾滋病是什么?艾滋病病毒 艾滋病病毒 艾滋病病毒没有NNIBP.在的药物设计中.分子对接的分子对接.分子动力学分子动力学

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