Structure–affinity relationships of the affinity of 2-pyrazolyl adenosine analogues for the adenosine A2A receptor (original) (raw)

Synthesis and biological data of 4-amino-1-(2-chloro-2-phenylethyl)-1 H-pyrazolo[3,4- b]pyridine-5-carboxylic acid ethyl esters, a new series of A 1-adenosine receptor (A 1AR) ligands

Paola Fossa

Bioorganic & Medicinal Chemistry Letters, 2001

View PDFchevron_right

Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: Effect of the N-5 bond type on the affinity and selectivity at the four adenosine receptor subtypes

Claudia Cusan

Purinergic Signalling, 2008

View PDFchevron_right

Pyrazolo Derivatives as Potent Adenosine Receptor Antagonists: An Overview on the Structure-Activity Relationships

Stephanie Federico

International Journal of Medicinal Chemistry, 2011

View PDFchevron_right

Pyrazolo[1 ',5 ':1,6]pyrimido[4,5-d]pyridazin-4(3H)-ones as selective human A(1) adenosine receptor ligands

Alessia Graziano, Letizia Crocetti, Maria Giovannoni

2010

View PDFchevron_right

Modulation of adenosine receptor affinity and intrinsic efficacy in adenine nucleosides substituted at the 2-position

Kenneth A Jacobson

Bioorganic & Medicinal Chemistry, 2004

View PDFchevron_right

Comparative molecular field analysis of selective A< sub> 3 adenosine receptor agonists

Suhaib Siddiqi

1995

View PDFchevron_right

2-Substituted adenosine derivatives: affinity and efficacy at four subtypes of human adenosine receptors

Kenneth A Jacobson

Biochemical Pharmacology, 2004

View PDFchevron_right

New base-altered adenosine analogues: Synthesis and affinity at adenosine A1 and A2A receptors

Kenneth A Jacobson

Bioorganic & Medicinal Chemistry Letters, 1997

View PDFchevron_right

Structure−Activity Relationships of 2, N 6 ,5‘-Substituted Adenosine Derivatives with Potent Activity at the A 2B Adenosine Receptor

Kenneth A Jacobson

Journal of Medicinal Chemistry, 2007

View PDFchevron_right

Pyrazolo [4, 3-e]-1, 2, 4-triazolo [1, 5-c] pyrimidine derivatives as adenosine receptor antagonists. Influence of the N5 substituent on the affinity at the human A3 and …

Hema Latha

Journal of medicinal …, 2003

View PDFchevron_right

Pharmacophore elucidation for a new series of 2-aryl-pyrazolo-triazolo-pyrimidines as potent human A 3 adenosine receptor antagonists

Priyankar Paira

Bioorganic & Medicinal Chemistry Letters, 2011

View PDFchevron_right

Further studies on pyrazolo[1',5':1,6]pyrimido[4,5-d]pyridazin-4(3H)-ones as potent and selective human A1 adenosine receptor antagonists

Gabriella Guerrini

European journal of medicinal chemistry, 2015

View PDFchevron_right

Antagonists of the human adenosine A2A receptor. Part 3: Design and synthesis of pyrazolo[3,4-d]pyrimidines, pyrrolo[2,3-d]pyrimidines and 6-arylpurines

Colin T Dourish

Bioorganic & Medicinal Chemistry Letters, 2008

View PDFchevron_right

Pyrrolo- and pyrazolo-[3,4-e][1,2,4]triazolo[1,5-c]pyrimidines as adenosine receptor antagonists

Pier Giovanni Baraldi

Bioorganic & Medicinal Chemistry, 2012

View PDFchevron_right

Adenosine receptors. Part 1 : (2S,3S,4R,5R)-2-(4-(alkyl/arylamino)-5Hpyrrolo[3,2-d]pyrimidin-7-yl)-5-(hydroxymethyl)pyrrolidine-3,4-diol derivatives as possible adenosine receptor agonists

Umesh Agrawal

2014

View PDFchevron_right

Water-Soluble Pyrazolo[4,3- e ][1,2,4]triazolo[1,5- c ]pyrimidines as Human A 3 Adenosine Receptor Antagonists

Sandro Cosconati

Journal of Medicinal Chemistry, 2012

View PDFchevron_right

Influence of the molecular structure of N6-(ω-aminoalkyl)adenosines on adenosine receptor affinity and intrinsic activity

Philip van Galen

European Journal of Pharmacology: Molecular Pharmacology, 1989

View PDFchevron_right

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

Gloria Cristalli

Bioorganic & Medicinal Chemistry Letters, 2001

View PDFchevron_right

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

Stephanie Federico

European journal of medicinal chemistry, 2015

View PDFchevron_right

N 6-Cycloalkyl-and N 6-Bicycloalkyl-C 5′(C 2′)-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A1 Adenosine Receptor with …

Antonio Lavecchia

Journal of medicinal …, 2009

View PDFchevron_right

Novel Pyrazolo[3,4-c]pyridine Antagonists with Nanomolar affinity for A1 / A3 Adenosine Receptors: Binding Kinetics and Exploration of their Binding Profile Using Mutagenesis Experiments, MD simulations and TI/MD calculations

Margarita Stampelou

View PDFchevron_right

Pyrazolo-triazolo-pyrimidine Scaffold as a Molecular Passepartout for the Pan-Recognition of Human Adenosine Receptors

Tatiana Da Ros

Biomolecules

View PDFchevron_right

Does the combination of optimal substitutions at the C 2-, N 5- and N 8-positions of the pyrazolo-triazolo-pyrimidine scaffold guarantee selective modulation of the human A 3 adenosine receptors

Silvia Paoletta

Bioorganic & Medicinal Chemistry, 2011

View PDFchevron_right

Synthesis, biological evaluation, and molecular modeling of ribose-modified adenosine analogues as adenosine receptor agonists

Riccardo Petrelli, Loredana Cappellacci, Mario Grifantini

Journal of Medicinal Chemistry, 2005

View PDFchevron_right

Discovery of simplified N2-substituted pyrazolo[3,4-d]pyrimidine derivatives as novel adenosine receptor antagonists: Efficient synthetic approaches, biological evaluations and molecular docking studies

Priyankar Paira

Bioorganic & Medicinal Chemistry, 2014

View PDFchevron_right

Medicinal Chemistry of the A3 Adenosine Receptor: Agonists, Antagonists, and Receptor Engineering

Kenneth A Jacobson

Handbook of Experimental Pharmacology, 2009

View PDFchevron_right

5′-Carbamoyl derivatives of 2′-C-methyl-purine nucleosides as selective A1 adenosine receptor agonists: Affinity, efficacy, and selectivity for A1 receptor from different species

Riccardo Petrelli, Loredana Cappellacci, Mario Grifantini

Bioorganic & Medicinal Chemistry, 2008

View PDFchevron_right