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研究人员设计了喹喔啉基和喹啉基化合物作为潜在的ALK5抑制剂,以靶向癌症治疗中的TGF-β通路

Researchers Design Quinoxalinyl and Quinolinyl Compounds as Potential ALK5 Inhibitors to Target TGF-β Pathway in Cancer Therapy

GeneOnline 等信源发布 2026-01-15 05:47

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Researchers have identified quinoxalinyl and quinolinyl compounds as potential inhibitors of ALK5 (Activin receptor-like kinase 5), a key component of the TGF-β signaling pathway associated with cancer development and tumor progression. The study, conducted by Liu, C., Li, J., and Lu, Y.Q., focuses on the design and synthesis of these compounds to target ALK5 effectively, marking a notable step in cancer therapeutic research..

研究人员已确定喹喔啉基和喹啉基化合物是ALK5(激活素受体样激酶5)的潜在抑制剂,ALK5是与癌症发展和肿瘤进展相关的TGF-β信号通路的关键组成部分。这项由刘畅、李杰和吕玉清进行的研究,专注于设计和合成这些化合物以有效靶向ALK5,标志着癌症治疗研究中的重要一步。

The investigation highlights the critical role of ALK5 in oncogenesis and its potential as a therapeutic target. By exploring the structural properties of quinoxalinyl and quinolinyl derivatives, researchers aim to disrupt the TGF-β signaling pathway that contributes to tumor growth. The findings provide insights into how these compounds interact with ALK5 at a molecular level, offering promising avenues for further drug development..

调查突显了ALK5在肿瘤发生中的关键作用及其作为治疗靶点的潜力。通过探索喹喔啉基和喹啉基衍生物的结构特性,研究人员旨在破坏促进肿瘤生长的TGF-β信号通路。这些发现提供了这些化合物如何在分子水平上与ALK5相互作用的见解,为药物的进一步开发提供了有前景的方向。

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Date: January 15, 2026

日期:2026年1月15日

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