N6-Substituted Adenosine Receptor Agonists. Synthesis and Pharmacological Activity as Potent Antinociceptive Agents-Reference-Cited by-同舟云学术

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N6-Substituted Adenosine Receptor Agonists. Synthesis and Pharmacological Activity as Potent Antinociceptive Agents

Published:1994-12 Issue:25 Volume:37 Page:4307-4316
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Gungor Timur,Malabre Patrice,Teulon Jean-Marie,Camborde Francoise,Meignen Joelle,Hertz Francoise,Virone-Oddos Angela,Caussade Francois,Cloarec Alix

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm00051a007

Cited by 26 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. Exploration of chalcones and related heterocycle compounds as ligands of adenosine receptors: therapeutics development;Molecular Diversity;2021-06-27

2. Synthetic Approaches to 3-(2-Nitroalkyl) Indoles and Their Use to Access Tryptamines and Related Bioactive Compounds;Chemical Reviews;2014-06-06

3. Synthesis, Crystal Structure and Evaluation of Cancer Inhibitory Activity of 4-[indol-3-yl-Methylene]-1H-pyrazol-5(4H)-one derivatives;Journal of Chemical Research;2012-12

4. Synthesis and Evaluation of 1-Amino-6-halo-β-carbolines as Antimalarial and Antiprion Agents;ChemMedChem;2012-01-24

5. Synthesis of Novel Rigid Analogs of Tryptamine as Potential Serotonin Ligands through Pd(0)-Catalyzed Diaryl Coupling Reactions;Synthetic Communications;2008-06-27

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