5‘-Substituted Adenosine Analogs as New High-Affinity Partial Agonists for the Adenosine A1 Receptor-Reference-Cited by-同舟云学术

5‘-Substituted Adenosine Analogs as New High-Affinity Partial Agonists for the Adenosine A1 Receptor

Published:1998-01-01 Issue:1 Volume:41 Page:102-108
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

van der Wenden Eleonora M.¹,Carnielli Marta¹,Roelen Harlof C. P. F.¹,Lorenzen Anna¹,von Frijtag Drabbe Künzel Jacobien K.¹,IJzerman Adriaan P.¹

Affiliation:

1. Div. Medicinal Chemistry, Leiden/Amsterdam Center for Drug Research, P.O. Box 9502, 2300 RA Leiden, The Netherlands, and Pharmakologisches Institut, Im Neuenheimer Feld 366, 69120 Heidelberg, Germany

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm970508l

Reference42 articles.

1. Jacobson, K. A.; Van Rhee, A. M. Development of selective purinoceptor agonists and antagonists.Purinergic approaches in experimentaltherapeutics; Jacobson, K. A., Jarvis, M. F., Eds.; Wiley-Liss: New York, 1997; pp 101−128.

2. Stiles, G. L. Adenosine receptor subtypes: new insights from cloning and functional studies.Purinergic approaches in experimental therapeutics; Jacobson, K. A., Jarvis, M. F., Eds.; Wiley-Liss: New York, 1997; pp 29−37.

3. Coronary vasoactivity of adenosine in the conscious dog.

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