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Updated: Jan 12, 2026

Method for Identifying Small Molecule Inhibitors of the Protein-protein Interaction Between HCN1 and TRIP8b
Published on: November 11, 2016
Small molecule inhibitors of the co-receptor neuropilin-1
Yu-Heng Liu1, Kang-Hui Liang2, Wen Zhang2
1College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, PR China; Zhejiang Key Laboratory of Green Manufacturing Technology for Chemical Drugs, Deqing 313200, PR China.
Abstract:
Neuropilin-1 (NRP-1) is a multifunctional cell surface receptor that acts as a co-receptor for vascular endothelial growth factor (VEGF), semaphorins (SEMAs), and transforming growth factor β (TGF-β), and is widely involved in various physiological and pathological processes such as neural development, angiogenesis, and immune regulation. In cancer treatment, NRP-1 has attracted extensive attention because of its key role in pathological angiogenesis, tumor immune escape, and tumor progression, and it is regarded as a potential therapeutic target for tumors. In recent years, the development of small molecule inhibitors of NRP-1 has become a new research strategy. This article reviews the research progress of small molecule inhibitors of NRP-1, classifying them into three different types of small molecules, and focuses on introducing ideas for their development, mechanisms of action, and research status. It provides guidance for the future development of small molecule inhibitors of NRP-1.
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