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International Union of Pharmacology. XXV. Nomenclature and classification of adenosine receptors

Pharmacological reviews, 2001-12, Vol.53 (4), p.527

2001

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Adenosine receptors and their ligands

Naunyn-Schmiedeberg's archives of pharmacology, 2000-11, Vol.362 (4-5), p.382-391

Klotz, K N

2000

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Comparative pharmacology of human adenosine receptor subtypes - characterization of stably transfected receptors in CHO cells

Naunyn-Schmiedeberg's archives of pharmacology, 1998-01, Vol.357 (1), p.1-9

1998

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Comparative pharmacology of human beta-adrenergic receptor subtypes--characterization of stably transfected receptors in CHO cells

Naunyn-Schmiedeberg's archives of pharmacology, 2004-02, Vol.369 (2), p.151-159

2004

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Navigating in chromone chemical space: discovery of novel and distinct A3 adenosine receptor ligands

RSC advances, 2015-09, Vol.5 (96), p.78572-78585

2015

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Novel 8-(p-substituted-phenyl/benzyl)xanthines with selectivity for the A2A adenosine receptor possess bronchospasmolytic activity

European journal of medicinal chemistry, 2014-03, Vol.75, p.327-335

2014

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Adenosine receptors and cancer

Handbook of experimental pharmacology, 2009 (193), p.399

2009

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Signaling by extracellular nucleotides and nucleosides

Naunyn-Schmiedeberg's archives of pharmacology, 2000-11, Vol.362 (4-5), p.295-298

2000

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A facile and novel synthesis of N(2)-, C(6)-substituted pyrazolo[3,4-d]pyrimidine-4 carboxylate derivatives as adenosine receptor antagonists

European journal of medicinal chemistry, 2015-03, Vol.92, p.784-798

2015

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A2B Adenosine Receptor Agonists: Synthesis and Biological Evaluation of 2-Phenylhydroxypropynyl Adenosine and NECA Derivatives

Nucleosides, nucleotides & nucleic acids, 2004-01, Vol.23 (1-2), p.471-481

2004

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Introduction of alkynyl chains on C-8 of adenosine led to very selective antagonists of the A3 adenosine receptor

Bioorganic & medicinal chemistry letters, 2001-07, Vol.11 (14), p.1931-1934

2001

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[(3)H]MRE 3008F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptors

Molecular pharmacology, 2000-05, Vol.57 (5), p.968-975

2000

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A carboxyl-terminal tail peptide of neutrophil chemotactic receptor disrupts its physical complex with G protein

Journal of leukocyte biology, 1993-12, Vol.54 (6), p.572-577

1993

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Adenosine receptor agonists: synthesis and binding affinity of 2- (aryl)alkylthioadenosine derivatives

ARKIVOC, 2004-04, Vol.2004 (5), p.301-311

2004

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Water-soluble phosphate prodrugs of 1-propargyl-8-styrylxanthine derivatives, A(2A)-selective adenosine receptor antagonists

Journal of medicinal chemistry, 2000-02, Vol.43 (3), p.440-448

2000

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8-cyclopentyl-1,3-dipropylxanthine (DPCPX)-a selective high affinity antagonist radioligand for A1 adenosine receptors

Naunyn-Schmiedeberg's archives of pharmacology, 1987-08, Vol.336 (2), p.204-210

1987

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Functional molecular complexes of human N-formyl chemoattractant receptors and actin

The Journal of immunology (1950), 1993-11, Vol.151 (10), p.5653-5665

1993

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Regulatory interaction of N-formyl peptide chemoattractant receptors with the membrane skeleton in human neutrophils

The Journal of immunology (1950), 1994-01, Vol.152 (2), p.801-810

1994

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Carbamazepine distinguishes between adenosine receptors that mediate different second messenger responses

European journal of pharmacology, 1991-04, Vol.206 (4), p.285-290

1991

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2-Alkynyl derivatives of adenosine and adenosine-5'-N-ethyluronamide as selective agonists at A2 adenosine receptors

Journal of medicinal chemistry, 1992-06, Vol.35 (13), p.2363-2368

1992

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Reconstitution of a physical complex between the N-formyl chemotactic peptide receptor and G protein. Inhibition by pertussis toxin-catalyzed ADP ribosylation

The Journal of biological chemistry, 1992-04, Vol.267 (11), p.7576-7581

1992

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Synthesis, biological and modeling studies of 1,3-di- n-propyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro [1,2,4]-triazolo [3,4-f]-purines as adenosine receptor antagonists

Farmaco (Società chimica italiana : 1989), 2005-08, Vol.60 (8), p.643-651

2005

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Chemical modification of A1 adenosine receptors in rat brain membranes. Evidence for histidine in different domains of the ligand binding site

The Journal of biological chemistry, 1988-11, Vol.263 (33), p.17522-17526

1988

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Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as highly potent and selective human A(3) adenosine receptor antagonists

Journal of medicinal chemistry, 1999-11, Vol.42 (22), p.4473-4478

1999

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Activation of the A3 adenosine receptor affects cell cycle progression and cell growth

Naunyn-Schmiedeberg's archives of pharmacology, 2000-03, Vol.361 (3), p.225-234

2000

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International Union of Pharmacology. XXV. Nomenclature and classification of adenosine receptors

Adenosine receptors and their ligands

Comparative pharmacology of human adenosine receptor subtypes - characterization of stably transfected receptors in CHO cells

Comparative pharmacology of human beta-adrenergic receptor subtypes--characterization of stably transfected receptors in CHO cells

Navigating in chromone chemical space: discovery of novel and distinct A3 adenosine receptor ligands

Novel 8-(p-substituted-phenyl/benzyl)xanthines with selectivity for the A2A adenosine receptor possess bronchospasmolytic activity

Adenosine receptors and cancer

Signaling by extracellular nucleotides and nucleosides

A facile and novel synthesis of N(2)-, C(6)-substituted pyrazolo[3,4-d]pyrimidine-4 carboxylate derivatives as adenosine receptor antagonists

A2B Adenosine Receptor Agonists: Synthesis and Biological Evaluation of 2-Phenylhydroxypropynyl Adenosine and NECA Derivatives

Introduction of alkynyl chains on C-8 of adenosine led to very selective antagonists of the A3 adenosine receptor

[(3)H]MRE 3008F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptors

A carboxyl-terminal tail peptide of neutrophil chemotactic receptor disrupts its physical complex with G protein

Adenosine receptor agonists: synthesis and binding affinity of 2- (aryl)alkylthioadenosine derivatives

Water-soluble phosphate prodrugs of 1-propargyl-8-styrylxanthine derivatives, A(2A)-selective adenosine receptor antagonists

8-cyclopentyl-1,3-dipropylxanthine (DPCPX)-a selective high affinity antagonist radioligand for A1 adenosine receptors

Functional molecular complexes of human N-formyl chemoattractant receptors and actin

Regulatory interaction of N-formyl peptide chemoattractant receptors with the membrane skeleton in human neutrophils

Carbamazepine distinguishes between adenosine receptors that mediate different second messenger responses

2-Alkynyl derivatives of adenosine and adenosine-5'-N-ethyluronamide as selective agonists at A2 adenosine receptors

Reconstitution of a physical complex between the N-formyl chemotactic peptide receptor and G protein. Inhibition by pertussis toxin-catalyzed ADP ribosylation

Synthesis, biological and modeling studies of 1,3-di- n-propyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro [1,2,4]-triazolo [3,4-f]-purines as adenosine receptor antagonists

Chemical modification of A1 adenosine receptors in rat brain membranes. Evidence for histidine in different domains of the ligand binding site

Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as highly potent and selective human A(3) adenosine receptor antagonists

Activation of the A3 adenosine receptor affects cell cycle progression and cell growth

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