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Design and Synthesis of 2,6-Disubstituted-4′-Selenoadenosine-5′-N,N-Dimethyluronamide Derivatives as Human A(3) Adenosine Receptor Antagonists

A new series of 4′-selenoadenosine-5′-N,N-dimethyluronamide derivatives as highly potent and selective human A(3) adenosine receptor (hA(3)AR) antagonists, is described. The highly selective A(3)AR agonists, 4′-selenoadenosine-5′-N-methyluronamides were successfully converted into selective antagoni...

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Bibliografski detalji
Izdano u:Pharmaceuticals (Basel)
Glavni autori: Choi, Hongseok, Jacobson, Kenneth A., Yu, Jinha, Jeong, Lak Shin
Format: Artigo
Jezik:Inglês
Izdano: MDPI 2021
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8071163/
https://ncbi.nlm.nih.gov/pubmed/33920062
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ph14040363
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