New 2-Arylpyrazolo[4,3-c]quinoline Derivatives as Potent and Selective Human A3 Adenosine Receptor Antagonists-Reference-Cited by-同舟云学术

New 2-Arylpyrazolo[4,3-c]quinoline Derivatives as Potent and Selective Human A3 Adenosine Receptor Antagonists

Published:2005-07-01 Issue:15 Volume:48 Page:5001-5008
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Baraldi Pier Giovanni¹,Tabrizi Mojgan Aghazadeh¹,Preti Delia¹,Bovero Andrea¹,Fruttarolo Francesca¹,Romagnoli Romeo¹,Zaid Naser Abdel¹,Moorman Allan R.¹,Varani Katia¹,Borea Pier Andrea¹

Affiliation:

1. Dipartimento di Scienze Farmaceutiche, Dipartimento di Medicina Clinica e Sperimentale-Sezione di Farmacologia, Università di Ferrara, 44100 Ferrara Italy, College of Pharmacy, An-Najah National University, Nablus, and King Pharmaceutical R & D, 4000 CentreGreen Way, Suite 300 Cary, North Carolina 27513

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm050125k

Reference40 articles.

1. P1 and P2 Purine and Pyrimidine Receptor Ligands

2. Adenosine receptors: new opportunities for future drugs

3. Molecular cloning and characterization of the human A3 adenosine receptor.

Cited by 68 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recent Progress in the Synthetic Methods of Pyrazoloquinoline Derivatives;Current Organic Chemistry;2024-01

2. Development and Applications of Chimera Platforms for Tyrosine Phosphorylation;ACS Central Science;2023-08-09

3. Development and applications of chimera platforms for tyrosine phosphorylation;2023-03-05

4. Cu(ii)-Mediated aerobic oxidative synthesis of sulfonated chromeno[4,3-c]pyrazol-4(2H)-ones;Organic & Biomolecular Chemistry;2022

5. Synthesis of various pyrazole-fused heterocyclic systems using pyrazole-4-carbaldehydes as versatile precursors;Arkivoc;2021-07-07