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Antonio Macchiarulo

University of Perugia
H指数:43
被引数:9,226

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Targeting oxysterol-binding protein (OSBP) as a novel strategy to inhibit herpes simplex virus 2 (HSV-2) replication: First structure-activity relationship study of antiviral cholenamide derivatives

靶向氧甾醇结合蛋白(OSBP)作为抑制单纯疱疹病毒2型(HSV-2)复制的新型策略:抗病毒胆酰胺衍生物的首个构效关系研究

2026-08-010
PRE
Synthesis and structure-activity relationship study of a library of 1-substituted [1,2,4]triazolo[4,3-a]quinolines as valuable chemical probes for paraxonase-2 (PON2)

1-取代的[1,2,4]三唑并[4,3-a]喹啉库的合成及构效关系研究,将其作为帕罗尼酶-2(PON2)的有价值的化学探针

2026-03-260
OA
Design, Synthesis, and Biological Characterization of Macromolecular Ester Prodrugs of a Selective Cyclooxygenase-2 Inhibitor

选择性环氧化酶-2抑制剂的大分子酯前药的设计、合成与生物特性研究

2025-11-010
OAAI
Optimization of potent, broad-spectrum, and specific anti-influenza compounds targeting RNA polymerase PA-PB1 heterodimerization
2024-11-012
PRE
A microbially produced AhR ligand promotes a Tph1-driven tolerogenic program in multiple sclerosis

微生物产生的AhR配体促进多发性硬化症的Tph1-driven耐受计划

2024-03-203
OAAI
Design, synthesis, and biological evaluation of first-in-class indomethacin-based PROTACs degrading SARS-CoV-2 main protease and with broad-spectrum antiviral activity

降解SARS-CoV-2主要蛋白酶并具有广谱抗病毒活性的基于吲哚美辛的PROTACs的设计,合成和生物学评价

2024-03-0110
OAAI
Combining Solid-State NMR with Structural and Biophysical Techniques to Design Challenging Protein-Drug Conjugates

将固态NMR与结构和生物物理技术相结合,以设计具有挑战性的蛋白质-药物缀合物

2023-06-220
OAAI
A multicentric consortium study demonstrates that dimethylarginine dimethylaminohydrolase 2 is not a dimethylarginine dimethylaminohydrolase
2023-06-099
OAAI