NovelN2-Substituted Pyrazolo[3,4-d]pyrimidine Adenosine A3Receptor Antagonists: Inhibition of A3-Mediated Human Glioblastoma Cell Proliferation†-Reference-Cited by-同舟云学术

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NovelN2-Substituted Pyrazolo[3,4-d]pyrimidine Adenosine A3Receptor Antagonists: Inhibition of A3-Mediated Human Glioblastoma Cell Proliferation†

Published:2010-05-27 Issue:10 Volume:53 Page:3954-3963
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Taliani Sabrina,La Motta Concettina,Mugnaini Laura,Simorini Francesca,Salerno Silvia,Marini Anna Maria,Da Settimo Federico,Cosconati Sandro,Cosimelli Barbara,Greco Giovanni,Limongelli Vittorio,Marinelli Luciana,Novellino Ettore,Ciampi Osele,Daniele Simona,Trincavelli Maria Letizia,Martini Claudia

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm901785w

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1. Pyrazolo[3,4‐d]pyrimidine‐based scaffolds as antibacterial agents: Synthetic strategies, reactions, and in vitro biological evaluation;Journal of Heterocyclic Chemistry;2023-04-28

2. Glioblastoma: Current Status, Emerging Targets, and Recent Advances;Journal of Medicinal Chemistry;2022-07-05

3. Bicyclic 5–6 Systems: Other Four Heteroatoms 2:2;Comprehensive Heterocyclic Chemistry IV;2022

4. Cancer biology and molecular genetics of A3 adenosine receptor;Oncogene;2021-11-08

5. Potent and selective A3 adenosine receptor antagonists bearing aminoesters as heterobifunctional moieties;RSC Medicinal Chemistry;2021

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