Nucleoside-based A3 adenosine receptor antagonists as drug candidates
Author:
Publisher
Clarivate Analytics (US)
Subject
Pharmacology (medical),Pharmacology
Cited by 7 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. N6-Substituted 5′-N-Methylcarbamoyl-4′-selenoadenosines as Potent and Selective A3 Adenosine Receptor Agonists with Unusual Sugar Puckering and Nucleobase Orientation;Journal of Medicinal Chemistry;2017-04-19
2. Design, synthesis, and anticancer activity of C8-substituted-4′-thionucleosides as potential HSP90 inhibitors;Bioorganic & Medicinal Chemistry;2016-08
3. Regio- and stereoselective synthesis of 2′-β-substituted-fluoroneplanocin A analogues as potential anticancer agents;Organic & Biomolecular Chemistry;2015
4. Recent Advances in the Synthesis of Carbocyclic Nucleosides via Ring-Closing Metathesis;Asian Journal of Organic Chemistry;2014-05-09
5. Recent Advances in Synthesis and Biological Activity of 4′-Thionucleosides;Chemical Synthesis of Nucleoside Analogues;2013-02-15
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