2006 | Orthogonal activation of the reengineered A3 adenosine receptor (neoceptor) using tailored nucleoside agonists | 정낙신 | Article |
2007 | Probing the binding site of the A1 adenosine receptor reengineered for orthogonal recognition by tailored nucleosides | 정낙신 | Article |
2011 | Regio- and stereoselective synthesis of truncated 3′- aminocarbanucleosides and their binding affinity at the A 3 adenosine receptor | 정낙신; 최원준 | Article |
2007 | Role of adenosine A3 receptors on CA1 hippocampal neurotransmission during oxygen-glucose deprivation episodes of different duration | 정낙신 | Article |
2008 | Selective A3 adenosine receptor antagonists derived from nucleosides containing a bicyclo[3.1.0]hexane ring system | 정낙신 | Article |
2007 | Stereoselective synthesis of 1′-functionalized-4′- thionucleosides | 정낙신 | Article |
2004 | Structural determinants of efficacy at A3 adenosine receptors: Modification of the ribose moiety | 정낙신 | Article |
2006 | Structure-activity relationships of 2-chloro-N6-substituted- 4′-thioadenosine-5′-uronamides as highly potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
2008 | Structure-activity relationships of 2-chloro-N6-substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as human A3 adenosine receptor antagonists | 정낙신; 최원준 | Article |
2009 | Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists | 정낙신; 이상국; 최원준 | Article |
2012 | Structure-activity relationships of truncated C2- or C8-substituted adenosine derivatives as dual acting A 2A and A 3 adenosine receptor ligands | 정낙신; 최선; 최원준 | Article |
2008 | Structure-activity relationships of truncated D- and L-4′- thioadenosine derivatives as species-independent A3 adenosine receptor antagonists | 정낙신; 이상국; 최원준 | Article |
2014 | Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N6-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonists | 정낙신; 하헌주; 최선 | Article |
2011 | Synthesis and binding affinity of homologated adenosine analogues as A3 adenosine receptor ligands | 정낙신; 최원준 | Article |
2008 | Synthesis and structure-activity relationship studies of tyrosine-based antagonists at the human P2X7 receptor | 정낙신 | Article |
2008 | Synthesis of 2-chloro-N6-substituted-4'-thioadenosine-5'-N, N-dialkyluronamides as potent and selective A3 adenosine receptor antagonists. | 정낙신; 최원준 | Article |
2005 | Synthesis of 3'-ureidoadenosines and their high binding affinity at the mutant A3 adenosine receptor. | 이강만; 정낙신 | Article |
2008 | Synthesis of 3′-acetamidoadenosine derivatives as potential A 3 adenosine receptor agonists | 정낙신; 최원준 | Article |
2005 | Synthesis of 3′-ureidoadenosine analogues and their binding affinity to the A3 adenosine receptor | 정낙신 | Conference Paper |
2007 | Synthesis of N6-Substituted 3′-ureidoadenosine derivatives as highly potent agonists at the mutant A3 adenosine receptor | 정낙신 | Conference Paper |
2005 | Synthesis of novel apio carbocyclic nucleoside analogues as selective A3 adenosine receptor agonists | 이강만; 정낙신 | Article |