NX-2127与依鲁替尼治疗b细胞恶性肿瘤的比较分析

Jeon Subin
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引用次数: 0

摘要

肿瘤学是一个不断变化的医学领域,不断发展创新的治疗方法。在过去的几十年里,小分子药物因其疗效、选择性和靶向细胞内蛋白质的能力而成为人们关注的焦点。小分子抑制剂(Small-molecule inhibitors, SMIs)是一种抑制参与肿瘤生长的蛋白质的小分子药物[1,2]。靶向嵌合体(Proteolysis targeting chimeras, PROTACs)是一种异功能分子,可降解参与肿瘤生长的蛋白质[3,4]。这两种治疗方法都彻底改变了肿瘤学领域,因为它们已被证明比传统治疗方法更有益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative analysis of NX-2127 and ibrutinib in treating B-cell malignancies
Oncology is an ever-changing field of medicine with the constant development of innovative treatments. Small-molecule drugs have entered the spotlight in the past few decades for their efficacy, selectivity, and ability to target intracellular proteins. Small-molecule inhibitors (SMIs) are small-molecule drugs that inhibit proteins involved in tumour growth [1,2]. Proteolysis targeting chimeras (PROTACs) are heterobifunctional molecules that degrade proteins involved in tumour growth [3,4]. Both treatments have revolutionized the field of oncology as they have proven to be more beneficial than traditional treatments.
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