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Bioorganic & Medicinal Chemistry|February 13, 2014
Discovery of simplified N²-substituted pyrazolo[3,4-d]pyrimidine derivatives as novel adenosine receptor antagonists: efficient synthetic approaches, biological evaluations and molecular docking studiesGopalakrishnan Venkatesan, Priyankar Paira, Siew Lee Cheong, et al.
International Journal of Molecular Sciences|September 28, 2021
A Computational Workflow for the Identification of Novel Fragments Acting as Inhibitors of the Activity of Protein Kinase CK1δGiovanni Bolcato, Eleonora Cescon, Matteo Pavan, et al.
Biomolecules|November 25, 2023
Pyrazolo-triazolo-pyrimidine Scaffold as a Molecular Passepartout for the Pan-Recognition of Human Adenosine ReceptorsVeronica Salmaso, Margherita Persico, Tatiana Da Ros, et al.
Bioorganic & Medicinal Chemistry Letters|December 4, 2012
Fluorescent ligands for adenosine receptorsEszter Kozma, P Suresh Jayasekara, Lucia Squarcialupi, et al.
International Journal of Medicinal Chemistry|May 9, 2015
Pyrazolo derivatives as potent adenosine receptor antagonists: an overview on the structure-activity relationshipsSiew Lee Cheong, Gopalakrishnan Venkatesan, Priyankar Paira, et al.
Farmaco (Societa Chimica Italiana : 1989)|January 18, 2005
Synthesis and biological evaluation of new phenidone analogues as potential dual cyclooxygenase (COX-1 and COX-2) and human lipoxygenase (5-LOX) inhibitorsClaudia Cusan, Giampiero Spalluto, Maurizio Prato, et al.
Medicinal Research Reviews|November 19, 2011
The A3 adenosine receptor as multifaceted therapeutic target: pharmacology, medicinal chemistry, and in silico approachesSiew Lee Cheong, Stephanie Federico, Gopalakrishnan Venkatesan, et al.
Farmaco (Societa Chimica Italiana : 1989)|April 26, 2005
Synthesis and biological evaluation of a new class of acyl derivatives of 3-amino-1-phenyl-4,5-dihydro-1H-pyrazol-5-one as potential dual cyclooxygenase (COX-1 and COX-2) and human lipoxygenase (5-LOX) inhibitorsClaudia Cusan, Giampiero Spalluto, Maurizio Prato, et al.
Bioorganic & Medicinal Chemistry Letters|April 23, 2011
Pharmacophore elucidation for a new series of 2-aryl-pyrazolo-triazolo-pyrimidines as potent human A3 adenosine receptor antagonistsSiew Lee Cheong, Stephanie Federico, Gopalakrishnan Venkatesan, et al.
Purinergic Signalling|April 12, 2008
New 2,6,9-trisubstituted adenines as adenosine receptor antagonists: a preliminary SAR profileCatia Lambertucci, Gloria Cristalli, Diego Dal Ben, et al.
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