“Reversine” and Its 2-Substituted Adenine Derivatives as Potent and Selective A3 Adenosine Receptor Antagonists-Reference-Cited by-同舟云学术

“Reversine” and Its 2-Substituted Adenine Derivatives as Potent and Selective A3 Adenosine Receptor Antagonists

Published:2005-07-01 Issue:15 Volume:48 Page:4910-4918
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Perreira Melissa¹,Jiang Jian-kang¹,Klutz Athena M.¹,Gao Zhan-Guo¹,Shainberg Asher¹,Lu Changrui¹,Thomas Craig J.¹,Jacobson Kenneth A.¹

Affiliation:

1. Chemical Biology Core Facility, and Molecular Recognition Section, Laboratory of Biological Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, and Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan, 52900, Israel

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm050221l

Reference34 articles.

1. (N)-Methanocarba 2,N6-Disubstituted Adenine Nucleosides as Highly Potent and Selective A3 Adenosine Receptor Agonists

2. The synthesis of new adenosine A3 selective ligands containing bioisosteric isoxazoles

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