Synthesis, Biological Evaluation, and Molecular Modeling of Ribose-Modified Adenosine Analogues as Adenosine Receptor Agonists-Reference-Cited by-同舟云学术

Synthesis, Biological Evaluation, and Molecular Modeling of Ribose-Modified Adenosine Analogues as Adenosine Receptor Agonists

Published:2005-02-05 Issue:5 Volume:48 Page:1550-1562
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Cappellacci Loredana¹,Franchetti Palmarisa¹,Pasqualini Michela¹,Petrelli Riccardo¹,Vita Patrizia¹,Lavecchia Antonio¹,Novellino Ettore¹,Costa Barbara¹,Martini Claudia¹,Klotz Karl-Norbert¹,Grifantini Mario¹

Affiliation:

1. Dipartimento di Scienze Chimiche, Università di Camerino, 62032 Camerino, Italy, Dipartimento di Chimica Farmaceutica e Tossicologica, Università di Napoli “Federico II”, 80131 Napoli, Italy, Dipartimento di Neurobiologia, Farmacologia e Biotecnologia, Università di Pisa, 56126 Pisa, Italy, and Institut für Pharmakologie und Toxikologie, Universität Würzburg, D-97078 Würzburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm049408n

Reference49 articles.

1. Adenosine receptors as targets for drug development

2. Modulation of hepatic glucose production by non-esterified fatty acids in Type 2 (non-insulin-dependent) diabetes mellitus

3. New, Non-Adenosine, High-Potency Agonists for the Human Adenosine A2B Receptor with an Improved Selectivity Profile Compared to the Reference Agonist N-Ethylcarboxamidoadenosine

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