| 2011 | Design, synthesis and anticancer activity of novel dihydrobenzofuro[4,5-b] [1,8]naphthyridin-6-one derivatives | 정낙신 | Article |
| 2003 | Design, synthesis and binding affinity of 3′-fluoro analogues of Cl-IB-MECA as adenosine A3 receptor ligands | 이승진; 정낙신 | Article |
| 2022 | Design, Synthesis and Biological Evaluation of 1,3,5-Triazine Derivatives Targeting hA(1) and hA(3) Adenosine Receptor | 유진하 | Article |
| 2017 | Design, synthesis and biological evaluation of 1,3-diphenylbenzo[f] [1,7]naphthyrdines | 권영주; 전규연 | Article |
| 2014 | Design, synthesis and biological evaluation of benzyl 2-(1H-imidazole-1-yl) pyrimidine analogues as selective and potent Raf inhibitors | 류재상 | Article |
| 2011 | Design, synthesis and docking study of 5-amino substituted indeno[1,2-c]isoquinolines as novel topoisomerase i inhibitors | 권영주 | Article |
| 2008 | Design, synthesis and evaluation of 2-phenyl-1H-benzo[d]imidazole-4,7-diones as vascular smooth muscle cell proliferation inhibitors | 유충규; 이상국 | Article |
| 2014 | Design, synthesis and systematic evaluation of cytotoxic 3-heteroarylisoquinolinamines as topoisomerases inhibitors | 권영주 | Article |
| 2011 | Design, Synthesis, and Anti-HCV Activity of 2 '-Modified-4 '-selenonucleosides | 정낙신; 최원준; 이혁우 | Meeting Abstract |
| 2007 | Design, synthesis, and anti-tumor activity of 4′-thionucleosides as potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
| 2016 | Design, synthesis, and anticancer activity of C8-substituted-4 '-thionucleosides as potential HSP90 inhibitors | 최선 | Article |
| 2007 | Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines | 정낙신; 이상국 | Meeting Abstract |
| 2005 | Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines. | 이강만; 정낙신; 이상국; 최원준 | Article |
| 2012 | Design, synthesis, and antitumor evaluation of 2,4,6-triaryl pyridines containing chlorophenyl and phenolic moiety | 권영주 | Article |
| 2010 | Design, synthesis, and binding of homologated truncated 4′-thioadenosine derivatives at the human A3 adenosine receptors | 정낙신; 최선; 최원준 | Article |
| 2006 | Design, synthesis, and biological activity of N6-substituted-4′-thioadenosines at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
| 2018 | Design, synthesis, and biological evaluation of 1,3-diarylisoquinolines as novel topoisomerase I catalytic inhibitors | 권영주 | Article |
| 2003 | Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
| 2004 | Design, synthesis, and biological evaluation of novel 2-pyridinyl-[1,2,4] triazoles as inhibitors of transforming growth factor β1 type 1 receptor | 김대기 | Article |
| 2008 | Design, synthesis, and biological evaluation of novel constrained meta-substituted phenyl propanoic acids as peroxisome proliferator-activated receptor α and γ dual agonists | 류재상 | Article |
