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Analytical Biochemistry|March 1, 2011
Comparison and optimization of transient transfection methods at human astrocytoma cell line 1321N1Gabriella Marucci, Carmen Lammi, Michela Buccioni, et al.European Journal of Medicinal Chemistry|July 14, 2020
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 agentsCostanza Ceni, Daniela Catarzi, Flavia Varano, et al.Bioorganic & Medicinal Chemistry|May 28, 2011
Synthesis, structure-affinity relationships, and molecular modeling studies of novel pyrazolo[3,4-c]quinoline derivatives as adenosine receptor antagonistsOmbretta Lenzi, Vittoria Colotta, Daniela Catarzi, et al.Journal of Medicinal Chemistry|June 8, 2017
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 SubtypeMatteo Falsini, Lucia Squarcialupi, Daniela Catarzi, et al.Bioorganic & Medicinal Chemistry|November 23, 2012
Pyrazolo[1,5-c]quinazoline derivatives and their simplified analogues as adenosine receptor antagonists: synthesis, structure-affinity relationships and molecular modeling studiesDaniela Catarzi, Vittoria Colotta, Flavia Varano, et al.European Journal of Medicinal Chemistry|May 22, 2013
Evaluation of adenine as scaffold for the development of novel P2X3 receptor antagonistsCatia Lambertucci, Mayya Sundukova, Dhuldeo D Kachare, et al.Pharmaceuticals (Basel, Switzerland)|April 23, 2022
4-Heteroaryl Substituted Amino-3,5-Dicyanopyridines as New Adenosine Receptor Ligands: Novel Insights on Structure-Activity Relationships and PerspectivesDaniela Catarzi, Flavia Varano, Erica Vigiani, et al.Scientific Reports|July 27, 2017
Fragment optimization for GPCRs by molecular dynamics free energy calculations: Probing druggable subpockets of the A 2A adenosine receptor binding sitePierre Matricon, Anirudh Ranganathan, Eugene Warnick, et al.Bioorganic & Medicinal Chemistry|November 11, 2008
Novel potent and highly selective human A(3) adenosine receptor antagonists belonging to the 4-amido-2-arylpyrazolo[3,4-c]quinoline series: molecular docking analysis and pharmacological studiesVittoria Colotta, Francesca Capelli, Ombretta Lenzi, et al.Biomolecules|November 27, 2024
Chaga Mushroom Triterpenoids Inhibit Dihydrofolate Reductase and Act Synergistically with Conventional Therapies in Breast CancerJunbiao Wang, Daniela Beghelli, Augusto Amici, et al.Pageof 10