Synthesis, structure-activity relationship study and molecular modeling of triazolo[4,5-d]pyrimidines targeting an intracellular allosteric binding site of various chemokine receptorsEuropean Journal of Medicinal ChemistryIF5.92026-01-240PRE
High-affinity ELR plus chemokine ligands show G protein bias over b-arrestin recruitment and receptor internalization in CXCR1 signaling高亲和力ELR加趋化因子配体在CXCR1信号传导中显示g蛋白偏向于b-arrestin募集和受体内化JOURNAL OF BIOLOGICAL CHEMISTRYIF3.92025-01-010OAAI
Systematic assessment of chemokine ligand bias at the human chemokine receptor CXCR2 indicates G protein bias over β-arrestin recruitment and receptor internalizationCELL COMMUNICATION AND SIGNALINGIF8.92024-01-173OAAI
Exploration of Pyrido[3,4-d]pyrimidines as Antagonists of the Human Chemokine Receptor CXCR2MOLECULESIF4.62023-02-232OAAI
Identification of novel chemotypes as CXCR2 antagonists via a scaffold hopping approach from a thiazolo[4,5-d]pyrimidineEUROPEAN JOURNAL OF MEDICINAL CHEMISTRYIF5.92022-05-019PRE
个人简介
教育背景
工作经历
荣誉奖项
未登录.png){kind=icon}
未登录个人简介教育背景工作经历荣誉奖项
研究方向