2,4,6-Trisubstituted Pyrimidines as a New Class of Selective Adenosine A1 Receptor Antagonists-Reference-Cited by-同舟云学术

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

Published:2004-11-13 Issue:26 Volume:47 Page:6529-6540
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Chang Lisa C. W.¹,Spanjersberg Ronald F.¹,von Frijtag Drabbe Künzel Jacobien K.¹,Mulder-Krieger Thea¹,van den Hout Gijs¹,Beukers Margot W.¹,Brussee Johannes¹,IJzerman Adriaan P.¹

Affiliation:

1. Division of Medicinal Chemistry, Leiden/Amsterdam Center for Drug Research, P.O. Box 9502, 2300 RA Leiden, The Netherlands

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm049448r

Reference48 articles.

1. 4-[(Carboxymethyl)oxy]- and 4-[(carboxymethyl)amino]-5,7-dichloroquinoline-2-carboxylic acid: new antagonists of the strychnine-insensitive glycine binding site on the N-methyl-D-aspartate (NMDA) receptor complex

2. The three binding domain model of adenosine receptors: molecular modeling aspects

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