Structure−Activity Relationships of Truncatedd- andl-4′-Thioadenosine Derivatives as Species-Independent A3Adenosine Receptor Antagonists(1)-Reference-Cited by-同舟云学术

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Structure−Activity Relationships of Truncatedd- andl-4′-Thioadenosine Derivatives as Species-Independent A3Adenosine Receptor Antagonists(1)

Published:2008-10-23 Issue:20 Volume:51 Page:6609-6613
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Jeong Lak Shin,Pal Shantanu,Choe Seung Ah,Choi Won Jun,Jacobson Kenneth A.,Gao Zhan-Guo,Klutz Athena M.,Hou Xiyan,Kim Hea Ok,Lee Hyuk Woo,Lee Sang Kook,Tosh Dilip K.,Moon Hyung Ryong

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm8008647

Cited by 41 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. Structure–Activity Relationship of Truncated 4′-Selenonucleosides: A₃ Adenosine Receptor Activity and Binding Selectivity;ACS Medicinal Chemistry Letters;2024-08-22

2. Biocatalytic Nucleobase Diversification of 4′‐Thionucleosides and Application of Derived 5‐Ethynyl‐4′‐thiouridine for RNA Synthesis Detection;Angewandte Chemie International Edition;2024-07-11

3. Biocatalytic Nucleobase Diversification of 4′‐Thionucleosides and Application of Derived 5‐Ethynyl‐4′‐thiouridine for RNA Synthesis Detection;Angewandte Chemie;2024-07-11

4. Structural insights into the agonist selectivity and structure-based engineering of the adenosine A3 receptor;2024-03-24

5. Current Strategies on the Enantioselective Synthesis of Modified Nucleosides;Synlett;2023-11-16

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