Author:
Buccioni Michela,Santinelli Claudia,Angeli Piero,Ben Diego,Lambertucci Catia,Thomas Ajiroghene,Volpini Rosaria,Marucci Gabriella
Publisher
Bentham Science Publishers Ltd.
Subject
Drug Discovery,Pharmacology,General Medicine
Cited by
5 articles.
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1. 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;European Journal of Medicinal Chemistry;2020-09
2. New A2A adenosine receptor antagonists: a structure-based upside-down interaction in the receptor cavity;Bioorganic Chemistry;2019-11
3. 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;Journal of Medicinal Chemistry;2019-08-27
4. Novel 8-amino-1,2,4-triazolo[4,3-a]pyrazin-3-one derivatives as potent human adenosine A1 and A2A receptor antagonists. Evaluation of their protective effect against β-amyloid-induced neurotoxicity in SH-SY5Y cells;Bioorganic Chemistry;2019-06
5. The 1,2,4-Triazolo[4,3-a]pyrazin-3-one as a Versatile Scaffold for the Design of Potent Adenosine Human Receptor Antagonists. Structural Investigations to Target the A2A Receptor Subtype;Journal of Medicinal Chemistry;2017-06-16