受体
肽
药理学
化学
医学
癌症研究
计算生物学
生物
生物化学
作者
Yung-Fong Tsai,Shun-Chin Yang,Tsong‐Long Hwang
标识
DOI:10.1080/13543776.2025.2515882
摘要
We examine newly disclosed patents concerning FPR modulators, with all specified compounds classified as either FPR1 or FPR2 modulators. Receptor cross-reactivity, ligand promiscuity, and receptor variations across species are challenges encountered during drug formulation. Further research into different types of biased agonists and the synthesis of potent and selective ligands is essential to overcome these obstacles and facilitate the eventual therapeutic use of biased signaling in inflammation and diseases.
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