2014 | Structure-activity relationships of 2′-modified-4′- selenoarabinofuranosyl-pyrimidines as anticancer agents | 정낙신 | Article |
2005 | Synthesis of 3′-ureidoadenosine analogues and their binding affinity to the A3 adenosine receptor | 정낙신 | Conference Paper |
2005 | A novel adenosine analog, thio-Cl-IB-MECA, induces G0/G 1 cell cycle arrest and apoptosis in human promyelocytic leukemia HL-60 cells | 정낙신; 이상국 | Article |
2005 | Stereoselective synthesis of conformationally rigid apio carbanucleosides as potential antiviral agents | 정낙신 | Conference Paper |
2012 | A straightforward synthesis of K-7174, a GATA-specific inhibitor | 정낙신 | Article |
2004 | Preparative synthesis of the key intermediate, (4R,5R)-3-Benzyloxymethyl-4, 5-isopropylidenedioxycyclopent-2-enone for carbocyclic nucleosides | 정낙신 | Article |
2004 | Synthesis of 5′-substituted fluoro-neplanocin A analogues: Importance of a hydrogen bonding donor at 5′-position for the inhibitory activity of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
2005 | Synthesis of 3'-ureidoadenosines and their high binding affinity at the mutant A3 adenosine receptor. | 이강만; 정낙신 | Article |
2001 | Synthesis of novel D- and L-3 '-deoxy-3 '-C-hydroxymethyl nucleoside with exocyclic methylene as potential ribonucleotide reductase inhibitor | 정낙신 | Article; Proceedings Paper |
2000 | Structural study of antisense dimers, modified adenosine-thymidine phosphorothioate | 정낙신 | Article |