Adenosine receptors as therapeutic targets

KA Jacobson, ZG Gao - Nature reviews Drug discovery, 2006 - nature.com
Adenosine receptors are major targets of caffeine, the most commonly consumed drug in the
world. There is growing evidence that they could also be promising therapeutic targets in a …

Multivariate analysis of food fraud: A review of NIR based instruments in tandem with chemometrics

HN Moghaddam, Z Tamiji, MA Lakeh… - Journal of Food …, 2022 - Elsevier
The increasing concerns toward the quality and health of food products have necessitated
accurate and precise analytical methods in order to guarantee the quality of food. It is …

New, Non-Adenosine, High-Potency Agonists for the Human Adenosine A2B Receptor with an Improved Selectivity Profile Compared to the Reference Agonist N …

MW Beukers, LCW Chang… - Journal of medicinal …, 2004 - ACS Publications
The adenosine A2B receptor is the least well characterized of the four known adenosine
receptor subtypes because of the absence of potent, selective agonists. Here, we present …

Adenosine receptors and cancer

P Fishman, S Bar-Yehuda, M Synowitz… - Adenosine Receptors in …, 2009 - Springer
Abstract The A 1, A 2A, A 2B and A 3 G-protein-coupled cell surface adenosine receptors
(ARs) are found to be upregulated in various tumor cells. Activation of the receptors by …

Progress in the pursuit of therapeutic adenosine receptor antagonists

S Moro, ZG Gao, KA Jacobson… - Medicinal research …, 2006 - Wiley Online Library
Ever since the discovery of the hypotensive and bradycardiac effects of adenosine,
adenosine receptors continue to represent promising drug targets. First, this is due to the fact …

Moonlighting adenosine deaminase: a target protein for drug development

A Cortés, E Gracia, E Moreno, J Mallol… - Medicinal research …, 2015 - Wiley Online Library
Interest in adenosine deaminase (ADA) in the context of medicine has mainly focused on its
enzymatic activity. This is justified by the importance of the reaction catalyzed by ADA not …

Design, Synthesis, and Biological Evaluation of New 8-Heterocyclic Xanthine Derivatives as Highly Potent and Selective Human A2B Adenosine Receptor …

PG Baraldi, MA Tabrizi, D Preti, A Bovero… - Journal of medicinal …, 2004 - ACS Publications
Here we report the synthesis of 8-heterocycle-substituted xanthines as potent and selective
A2B adenosine receptor antagonists. The structure− activity relationships (SAR) of the …

2,4,6-Trisubstituted Pyrimidines as a New Class of Selective Adenosine A1 Receptor Antagonists

LCW Chang, RF Spanjersberg… - Journal of medicinal …, 2004 - ACS Publications
Adenosine receptor antagonists usually possess a bi-or tricyclic heteroaromatic structure at
their core with varying substitution patterns to achieve selectivity and/or greater affinity …

Recent progress in the development of adenosine receptor ligands as antiinflammatory drugs

R Akkari, JC Burbiel, J Hockemeyer… - Current topics in …, 2006 - ingentaconnect.com
Adenosine receptors belong to the family of G protein-coupled receptors. Four distinct
subtypes are known, termed A1, A2A, A2B and A3. Adenosine is an important signaling …

N6-[(Hetero) aryl/(cyclo) alkyl-carbamoyl-methoxy-phenyl]-(2-chloro)-5′-N-ethylcarboxamido-adenosines: The first example of adenosine-related structures with …

PG Baraldi, D Preti, MA Tabrizi, F Fruttarolo… - Bioorganic & medicinal …, 2007 - Elsevier
A new series of N6-[(hetero) aryl/(cyclo) alkyl-carbamoyl-methoxy-phenyl]-(2-chloro)-5′-N-
ethylcarboxamido-adenosines (24–43) has been synthesised and tested in binding assays …