au.\*:("CHINN, Moshe")
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Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonistsPAL, Shantanu; WON JUN CHOI; LAK SHIN JEONG et al.Bioorganic & medicinal chemistry. 2009, Vol 17, Num 10, pp 3733-3738, issn 0968-0896, 6 p.Article
2-Dialkynyl derivatives of (N)-methanocarba nucleosides: 'Clickable' A3 adenosine receptor-selective agonistsTOSH, Dilip K; CHINN, Moshe; YOO, Lena S et al.Bioorganic & medicinal chemistry. 2010, Vol 18, Num 2, pp 508-517, issn 0968-0896, 10 p.Article
Design and synthesis of N6-substituted-4'-thioadenosine-5'-uronamides as potent and selective human A3 adenosine receptor agonistsWON JUN CHOI; HYUK WOO LEE; HEA OK KIM et al.Bioorganic & medicinal chemistry. 2009, Vol 17, Num 23, pp 8003-8011, issn 0968-0896, 9 p.Article
Functionalized Congeners of A3 Adenosine Receptor-Selective Nucleosides Containing a Bicyclo[3.1.0]hexane Ring SystemTOSH, Dilip K; CHINN, Moshe; IVANOV, Andrei A et al.Journal of medicinal chemistry (Print). 2009, Vol 52, Num 23, pp 7580-7592, issn 0022-2623, 13 p.Article