抑制非酒精性脂肪性肝炎的新药设计

Soykan Agar, B. Akkurt, E. Ulukaya
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引用次数: 0

摘要

通过计算机辅助药物设计技术,一种名为INASHD的全新设计生物大分子被用于特异性靶向β2-pectrin,从而有效抑制和预防NASH疾病。利用先进的分子对接和分子动力学(MD)技术计算软件工具,展示了该药物有效抑制和控制β2-spectrin的α螺旋拓扑结构的卓越能力。这种蛋白质是疾病途径中的重要组成部分。我们成功设计出了一种有效抑制β2-spectrin的药物,其抑制分数超过了科学文献中记载的任何其他分子。在经过验证的计算软件的有力支持下,这种生物有机结构具有重大价值,并可因其创新设计而申请专利。在体外、体内、体外和人体阶段研究等各个阶段,它都显示出取得积极成果的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Drug Design to Suppress Nonalcoholic Steatohepatitis
A de novo designed biomolecule called INASHD was utilized through computer-aided drug design techniques to specifically target β2-spectrin, effectively suppressing and preventing NASH disease. Advanced computational software tools concerning the technologies of molecular docking and molecular dynamics (MD), were employed to showcase the drug's remarkable ability to efficiently suppress and control the α-helical topology of β2-spectrin. This protein is a vital component within the disease pathway. We successfully devised an effective design suppressing β2-spectrin, exhibiting an inhibition score surpassing any other molecule documented in scientific literature. With robust support from validated computational software, this bioorganic structure holds significant value and can be applied for a patent due to its innovative design. It shows promising potential for delivering positive outcomes in various stages, including in vitro, in vivo, ex vivo, and human phase studies.
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