2-Triazole-Substituted Adenosines: A New Class of Selective A3 Adenosine Receptor Agonists, Partial Agonists, and Antagonists-Reference-Cited by-同舟云学术

2-Triazole-Substituted Adenosines: A New Class of Selective A3 Adenosine Receptor Agonists, Partial Agonists, and Antagonists

Published:2006-11-15 Issue:25 Volume:49 Page:7373-7383
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Cosyn Liesbet¹,Palaniappan Krishnan K.¹,Kim Soo-Kyung¹,Duong Heng T.¹,Gao Zhan-Guo¹,Jacobson Kenneth A.¹,Van Calenbergh Serge¹

Affiliation:

1. Laboratory for Medicinal Chemistry, Faculty of Pharmaceutical Sciences (FFW), Ghent University, Harelbekestraat 72, B-9000 Ghent, Belgium, and Molecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm0608208

Reference50 articles.

1. Cloned adenosine A3 receptors: Pharmacological properties, species differences and receptor functions

2. Adenosine receptors as therapeutic targets

3. Pharmacology and Therapeutic Applications of A3 Receptor Subtype

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