1,2,4-Triazolo[1,5-a]quinoxaline as a Versatile Tool for the Design of Selective Human A3 Adenosine Receptor Antagonists: Synthesis, Biological Evaluation, and Molecular Modeling Studies of 2-(Hetero)aryl- and 2-Carboxy-Substitued Derivatives-Reference-Cited by-同舟云学术

1,2,4-Triazolo[1,5-a]quinoxaline as a Versatile Tool for the Design of Selective Human A3 Adenosine Receptor Antagonists: Synthesis, Biological Evaluation, and Molecular Modeling Studies of 2-(Hetero)aryl- and 2-Carboxy-Substitued Derivatives

Published:2005-11-11 Issue:25 Volume:48 Page:7932-7945
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Catarzi Daniela¹,Colotta Vittoria¹,Varano Flavia¹,Lenzi Ombretta¹,Filacchioni Guido¹,Trincavelli Letizia¹,Martini Claudia¹,Montopoli Christian¹,Moro Stefano¹

Affiliation:

1. Dipartimento di Scienze Farmaceutiche, Università degli Studi di Firenze, Polo Scientifico, Via U. Schiff, 6-50019 Sesto Fiorentino, Firenze, Italy, Dipartimento di Psichiatria, Neurobiologia, Farmacologia e Biotecnologie, Università degli Studi di Pisa, Via Bonanno, 6-50126 Pisa, Italy, Molecular Modeling Section, Dipartimento di Scienze Farmaceutiche, Università degli Studi di Padova, via Marzolo 5, 35131 Padova, Italy

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm0504149

Reference62 articles.

1. The role of receptor structure in determining adenosine receptor activity

2. Structure and function of adenosine receptors and their genes

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