2-(Benzimidazol-2-yl)quinoxalines: A Novel Class of Selective Antagonists at Human A1 and A3 Adenosine Receptors Designed by 3D Database Searching-Reference-Cited by-同舟云学术

2-(Benzimidazol-2-yl)quinoxalines: A Novel Class of Selective Antagonists at Human A1 and A3 Adenosine Receptors Designed by 3D Database Searching

Published:2005-11-11 Issue:26 Volume:48 Page:8253-8260
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Novellino Ettore¹,Cosimelli Barbara¹,Ehlardo Marina¹,Greco Giovanni¹,Iadanza Manuela¹,Lavecchia Antonio¹,Rimoli Maria Grazia¹,Sala Annalisa¹,Da Settimo Antonio¹,Primofiore Giampaolo¹,Da Settimo Federico¹,Taliani Sabrina¹,La Motta Concettina¹,Klotz Karl-Norbert¹,Tuscano Daniela¹,Trincavelli Maria Letizia¹,Martini Claudia¹

Affiliation:

1. Dipartimento di Chimica Farmaceutica e Tossicologica, Università di Napoli “Federico II”, Via D. Montesano, 49, 80131 Napoli, Italy, Dipartimento di Scienze Farmaceutiche, Università di Pisa, Via Bonanno 6, 56126 Pisa, Italy, Institut für Pharmakologie und Toxikologie, Universität Würzburg, Versbacher Strasse 9, 97078 Würzburg, Germany, and Dipartimento di Psichiatria, Neurobiologia, Farmacologia e Biotecnologie, Università di Pisa, Via Bonanno 6, 56126 Pisa, Italy

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm050792d

Reference44 articles.

1. Targeting Adenosine Receptors

2. Role of Interstitial ATP and Adenosine in the Regulation of Renal Hemodynamics and Microvascular Function

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