Medicinal Chemistry of the A3 Adenosine Receptor-Reference-Cited by-同舟云学术

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Medicinal Chemistry of the A3 Adenosine Receptor

Published:2018 Issue: Volume: Page:169-198
ISSN:
Container-title:The Adenosine Receptors
language:
Short-container-title:

Author:

Jacobson Kenneth A.,Tosh Dilip K.,Gao Zhan-Guo,Yu Jinha,Suresh Rama R.,Rao Harsha,Romagnoli Romeo,Baraldi Pier Giovanni,Aghazadeh Tabrizi Mojgan

Publisher

Springer International Publishing

Link

http://link.springer.com/content/pdf/10.1007/978-3-319-90808-3_7

Reference139 articles.

1. Alnouri MW, Jepards S, Casari A et al (2015) Selectivity is species-dependent: characterization of standard agonists and antagonists at human, rat, and mouse adenosine receptors. Purinergic Signal 11:389–407

2. Baltos JA, Paoletta S, Nguyen ATN et al (2016) Structure-activity analysis of biased agonism at the human adenosine A3 receptor. Mol Pharmacol 90:12–22

3. Baraldi PG, Cacciari B, Pineda de las Infantas MJ et al (1998) Synthesis and biological activity of a new series of N6-arylcarbamoyl-,2-(ar)alkynyl-N6-arylcarbamoyl, and N6-carboxamido- derivatives of adenosine-5′-N-ethyluronamide (NECA) as A1 and A3 adenosine receptor agonists. J Med Chem 41:3174–3185

4. Baraldi PG, Cacciari B, Romagnoli R et al (2000) Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives as highly potent and selective human A3 adenosine receptor antagonists: influence of the chain at the N8 pyrazole nitrogen. J Med Chem 43:4768–4780

5. Baraldi PG, Tabrizi MA, Preti D et al (2005) New 2-arylpyrazolo[4,3-c]quinoline derivatives as potent and selective human A3 adenosine receptor antagonists. J Med Chem 48:5001–5008

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1. A3 Adenosine Receptor Ligands: From Discovery to Clinical Trials;Topics in Medicinal Chemistry;2023

2. Selective A₃ Adenosine Receptor Antagonist Radioligand for Human and Rodent Species;ACS Medicinal Chemistry Letters;2022-03-02

3. Medicinal chemistry of P2 and adenosine receptors: Common scaffolds adapted for multiple targets;Biochemical Pharmacology;2021-05

4. Purinergic Signaling: Impact of GPCR Structures on Rational Drug Design;ChemMedChem;2020-09-18

5. Truncated (N)-Methanocarba Nucleosides as Partial Agonists at Mouse and Human A3 Adenosine Receptors: Affinity Enhancement by N6-(2-Phenylethyl) Substitution;Journal of Medicinal Chemistry;2020-04-09

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