Structure−Activity Relationships of 2-Chloro-N6-substituted-4‘-thioadenosine-5‘-uronamides as Highly Potent and Selective Agonists at the Human A3 Adenosine Receptor-Reference-Cited by-同舟云学术

Structure−Activity Relationships of 2-Chloro-N6-substituted-4‘-thioadenosine-5‘-uronamides as Highly Potent and Selective Agonists at the Human A3 Adenosine Receptor

Published:2005-11-19 Issue:1 Volume:49 Page:273-281
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Jeong Lak Shin¹,Lee Hyuk Woo¹,Jacobson Kenneth A.¹,Kim Hea Ok¹,Shin Dae Hong¹,Lee Jeong A¹,Gao Zhan-Guo¹,Lu Changrui¹,Duong Heng T.¹,Gunaga Prashantha¹,Lee Sang Kook¹,Jin Dong Zhe¹,Chun Moon Woo¹,Moon Hyung Ryong¹

Affiliation:

1. Laboratory of Medicinal Chemistry, College of Pharmacy, Ewha Womans University, Seoul 120-750, Korea, College of Pharmacy, Seoul National University, Seoul 151-742, Korea, Molecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes, and Digestive and Kidney Disease, National Institute of Health, Bethesda, Maryland 20892, and College of Pharmacy, Pusan National University, Pusan 609-753, Korea

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm050595e

Reference26 articles.

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