Pyrazolo[3,4-d]pyrimidines; adenosine receptor selectivity
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry
Reference18 articles.
1. Pyrazolo [3,4-d] pyrimidines, a new class of adenosine antagonists
2. Pyrazolo[3, 4-]pyrimidines as adenosine antagonists
3. A novel synthesis of xanthines: support for a new binding mode for xanthines with respect to adenosine at adenosine receptors
4. A model for the antagonist binding site on the adenosine A1 receptor, based on steric, electrostatic, and hydrophobic properties
5. A steric and electrostatic comparison of three models for the agonist/antagonist binding site on the adenosine A1 receptor
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1. Synthesis, design, and antiproliferative evaluation of 6-(N-Substituted-methyl)pyrazolo[3,4-d]pyrimidines as the potent anti-leukemia agents;Bioorganic Chemistry;2024-07
2. Efficient acid catalytic synthesis of pyrazolopyrimidines from 1H-pyrazol-5-yl-N,N-dimethylformamidines with cyanamide;Tetrahedron;2018-05
3. One-pot synthesis and antiproliferative evaluation of pyrazolo[3,4-d]pyrimidine derivatives;Tetrahedron;2012-11
4. ChemInform Abstract: Pyrazolo(3,4-d)pyrimidines; Adenosine Receptor Selectivity.;ChemInform;2010-08-12
5. NovelN2-Substituted Pyrazolo[3,4-d]pyrimidine Adenosine A3Receptor Antagonists: Inhibition of A3-Mediated Human Glioblastoma Cell Proliferation†;Journal of Medicinal Chemistry;2010-05-27
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