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Publications by Mario Grifantini
N6-Cycloalkyl- AndN6-Bicycloalkyl-C5′(C2′)-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A1Adenosine Receptor With Antinociceptive Effects in Mice
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Related publications
Structure-Based Design, Synthesis, and in Vivo Antinociceptive Effects of Selective A1 Adenosine Receptor Agonists
Purine (N)Methanocarba Nucleoside Derivatives Lacking an Exocyclic Amine as Selective A3 Adenosine Receptor Agonists
Purine (N)Methanocarba Nucleoside Derivatives Lacking an Exocyclic Amine as Selective A3 Adenosine Receptor Agonists
2-Dialkynyl Derivatives of (N)-Methanocarba Nucleosides: ‘Clickable’ A3 Adenosine Receptor-Selective Agonists
Bioorganic and Medicinal Chemistry
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
Tricyclic Imidazoline Derivatives as Potent and Selective Adenosine A1 Receptor Antagonists
Exploring Distal Regions of the A3 Adenosine Receptor Binding Site: Sterically Constrained N6-(2-Phenylethyl)adenosine Derivatives as Potent Ligands
Bioorganic and Medicinal Chemistry
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
Extended N6 Substitution of Rigid C2-Arylethynyl Nucleosides for Exploring the Role of Extracellular Loops in Ligand Recognition at the A3 Adenosine Receptor
Bioorganic and Medicinal Chemistry Letters
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
The Adenosine A1 and A2A Receptor Affinity of a Series of 3,4-Dihydropyrimidone Derivatives
Suid-Afrikaanse Tydskrif vir Natuurwetenskap en Tegnologie
Biarylaniline Phenethanolamines as Potent and Selective B3 Adrenergic Receptor Agonists
