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Daniela Catarzi

University of Florence
H指数:32
被引数:2,628

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Design, synthesis, and pharmacological evaluation of thiazolo[5,4-d]pyrimidines hybridized with lipoic acid or catechol. Novel A2A adenosine receptor antagonists in neuroinflammatory diseases

噻唑并[5,4-d]嘧啶与硫辛酸或儿茶酚杂合物的设计、合成与药理学评价:神经炎症疾病中的新型A2A腺苷受体拮抗剂

2026-06-010
OAAI
8-Amino-1,2,4-triazolo[4,3-a]pyrazin-3-one derivatives hybridized with antioxidants: new highly potent and selective human A2A adenosine receptor antagonists as useful agents against cerebral ischemia

8-氨基-1,2,4-三唑并[4,3-a]吡嗪-3-酮衍生物与抗氧化剂杂化的化合物:作为有效对抗脑缺血的新型高活性、高选择性人A2A腺苷受体拮抗剂

2025-08-060
OA
Structural Investigations on 2-Amidobenzimidazole Derivatives as New Inhibitors of Protein Kinase CK1 Delta

2-氨基苯并咪唑衍生物作为蛋白激酶CK1 δ 的新抑制剂的结构研究

2024-04-070
OAAI
Dual Anta-Inhibitors of the A2A Adenosine Receptor and Casein Kinase CK1delta: Synthesis, Biological Evaluation, and Molecular Modeling Studies

A2A腺苷受体和酪蛋白激酶CK1delta的双重Anta抑制剂: 合成,生物学评估和分子模型研究

2023-01-237
OAAI
Discovery of first-in-class multi-target adenosine A2A receptor antagonists-carbonic anhydrase IX and XII inhibitors. 8-Amino-6-aryl-2-phenyl-1,2,4-triazolo [4,3-a]pyrazin-3-one derivatives as new potential antitumor agents
2020-09-018
OAAI
Adenosine A2B receptors inhibit K+ currents and cell differentiation in cultured oligodendrocyte precursor cells and modulate sphingosine-1-phosphate signaling pathway
2020-07-0121
PREAI
Antioxidant-Conjugated 1,2,4-Triazolo[4,3-a]pyrazin-3-one Derivatives: Highly Potent and Selective Human A2A Adenosine Receptor Antagonists Possessing Protective Efficacy in Neuropathic Pain
2019-08-2716
OAAI