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Publications by P. Towers

Radiolabeling and Efficient Synthesis of Tritiated 2-Chloro-N6-(3-Iodobenzyl)adenosine-5′-N-Methyluron-Amide, a Potent, Selective A3 Adenosine Receptor Agonist

Journal of Labelled Compounds and Radiopharmaceuticals

English

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Exploring Distal Regions of the A3 Adenosine Receptor Binding Site: Sterically Constrained N6-(2-Phenylethyl)adenosine Derivatives as Potent Ligands

Bioorganic and Medicinal Chemistry

Clinical Biochemistry

Pharmaceutical Science

Drug Discovery

2004

English

Metabolic Mapping of A3 Adenosine Receptor Agonist MRS5980

Biochemical Pharmacology

Biochemistry

Pharmacology

2015

English

Protection Against Ischemic Damage by Adenosine Amine Congener, a Potent and Selective Adenosine A1 Receptor Agonist

European Journal of Pharmacology

Pharmacology

1999

English

2-Dialkynyl Derivatives of (N)-Methanocarba Nucleosides: ‘Clickable’ A3 Adenosine Receptor-Selective Agonists

Bioorganic and Medicinal Chemistry

Clinical Biochemistry

Pharmaceutical Science

Drug Discovery

2010

English

A Selective Agonist Affinity Label for A3 Adenosine Receptors

Biochemical and Biophysical Research Communications

English

Synthesis of (R)-3,4-Dihydro-2h-Pyran-2-Carboxaldehyde: Application to the Synthesis of Potent Adenosine A2A and A3 Receptor Agonist

English

The Synthesis of the Metabolites of 2′,3′,5′-Tri-O-Acetyl-N6-(3-Hydroxyphenyl) Adenosine (WS070117)

Theoretical Chemistry

Pharmaceutical Science

English

Putative Role of the Adenosine A3 Receptor in the Antiproliferative Action of N 6-(2-Isopentenyl)adenosine

Purinergic Signalling

Molecular Neuroscience

English

4-Amido-2-Aryl-1, 2, 4-Triazolo[4, 3-A]quinoxalin-1-Ones as New Potent and Selective Human A3 Adenosine Receptor Antagonists. Synthesis, Pharmacological Evaluation, and Ligand-Receptor Modeling Studies

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by P. Towers

Radiolabeling and Efficient Synthesis of Tritiated 2-Chloro-N6-(3-Iodobenzyl)adenosine-5′-N-Methyluron-Amide, a Potent, Selective A3 Adenosine Receptor Agonist

Related publications

Exploring Distal Regions of the A3 Adenosine Receptor Binding Site: Sterically Constrained N6-(2-Phenylethyl)adenosine Derivatives as Potent Ligands

Metabolic Mapping of A3 Adenosine Receptor Agonist MRS5980

Protection Against Ischemic Damage by Adenosine Amine Congener, a Potent and Selective Adenosine A1 Receptor Agonist

2-Dialkynyl Derivatives of (N)-Methanocarba Nucleosides: ‘Clickable’ A3 Adenosine Receptor-Selective Agonists

A Selective Agonist Affinity Label for A3 Adenosine Receptors

Synthesis of (R)-3,4-Dihydro-2h-Pyran-2-Carboxaldehyde: Application to the Synthesis of Potent Adenosine A2A and A3 Receptor Agonist

The Synthesis of the Metabolites of 2′,3′,5′-Tri-O-Acetyl-N6-(3-Hydroxyphenyl) Adenosine (WS070117)

Putative Role of the Adenosine A3 Receptor in the Antiproliferative Action of N 6-(2-Isopentenyl)adenosine

4-Amido-2-Aryl-1, 2, 4-Triazolo[4, 3-A]quinoxalin-1-Ones as New Potent and Selective Human A3 Adenosine Receptor Antagonists. Synthesis, Pharmacological Evaluation, and Ligand-Receptor Modeling Studies