1166277-74-2Relevant academic research and scientific papers
Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists
Pal, Shantanu,Choi, Won Jun,Choe, Seung Ah,Heller, Cara L.,Gao, Zhan-Guo,Chinn, Moshe,Jacobson, Kenneth A.,Hou, Xiyan,Lee, Sang Kook,Kim, Hea Ok,Jeong, Lak Shin
, p. 3733 - 3738 (2009)
On the basis of potent and selective binding affinity of truncated 4′-thioadenosine derivatives at the human A3 adenosine receptor (AR), their bioisosteric 4′-oxo derivatives were designed and synthesized from commercially available 2,3-O-isopr
