| 2010 | 5,5 '-Substituted indirubin-3 '-oxime derivatives as potent cyclin-dependent kinase inhibitors with anticancer activity | 이상국 | Meeting Abstract |
| 2010 | 5,5′-substituted indirubin-3′-oxime derivatives as potent cyclin-dependent kinase inhibitors with anticancer activity | 이상국 | Article |
| 2000 | 5-Arylamino-2-methyl-4,7-dioxobenzothiazoles as inhibitors of cyclin-dependent kinase 4 and cytotoxic agents | 유충규; 이상국 | Article |
| 2004 | 6-Arylamino-7-chloro-quinazoline-5,8-diones as novel cytotoxic and DNA topoisomerase inhibitory agents | 유충규; 이상국 | Article |
| 2004 | A new cytotoxic phenylbutenoid dimer from the rhizomes of Zingiber cassumunar | 이상국; 서은경; 한아름 | Article |
| 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 |
| 2003 | A potential cytotoxic principle of Zingiber cassumunar | 이상국; 서은경; 한아름 | Article |
| 2012 | Anti-proliferative activity and suppression of P-glycoprotein by (-)-antofine, a natural phenanthroindolizidine alkaloid, in paclitaxel-resistant human lung cancer cells | 이상국 | Article |
| 2005 | Antibacterial and antifungal activity of pinosylvin, a constituent of pine | 이강만; 이상국 | Article |
| 2008 | Antioxidant, antiinflamatory, and antiproliferative activities of strawberry extracts | 이상국; 박헌주 | Article |
| 2008 | Antiproliferative effects of dibenzocyclooctadiene lignans isolated from Schisandra chinensis in human cancer cells | 이상국 | Article |
| 2004 | Asymmetric Total Syntheses of (-)-Antofine and (-)-Cryptopleurine Using (R)-(E)-4-(Tributylstannyl)but-3-en-2-ol | 이상국 | Article |
| 2004 | Baicalin induces NAD(P)H:quinone reductase through the transactivation of AP-1 and NF-κB in Hepa 1c1c7 cells | 이상국 | Article |
| 2004 | Biologic evaluation of curcumin and structural derivatives in cancer chemoprevention model systems | 이상국 | Article |
| 2003 | Comparative molecular field analysis study of stilbene derivatives active against A549 lung carcinoma | 이상국 | Article |
| 2005 | Cyclooxygenase-2 inhibitory phenylbutenoids from the rhizomes of Zingiber cassumunar | 이상국; 서은경; 한아름 | Article |
| 2002 | Cytotoxic activities of indigenous plant extracts in cultured human cancer cells | 이상국 | Article |
| 2003 | Cytotoxic activity and G2/M cell cycle arrest mediated by antofine, a phenanthroindolizidine alkaloid isolated from Cynanchum paniculatum | 이상국 | Article |
| 2003 | Cytotoxicity and DNA topoisomerase inhibitory activity of benz[f]indole-4,9-dione analogs | 김춘미; 김화정; 이상국; 서은경 | Article |
| 2010 | Daphnane diterpene esters with anti-proliferative activities against human lung cancer cells from Daphne genkwa | 이상국; 서은경 | Article |
| 2009 | Decursin and decursinol inhibit VEGF-induced angiogenesis by blocking the activation of extracellular signal-regulated kinase and c-Jun N-terminal kinase | 이상국 | Article |
| 2007 | Design, docking, and synthesis of novel indeno[1,2-c]isoquinolines for the development of antitumor agents as topoisomerase I inhibitors | 이상국; 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 |
| 2007 | Design, synthesis, and anti-tumor activity of 4′-thionucleosides as potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | 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 |
| 2006 | Design, synthesis, and biological activity of N6-substituted-4′-thioadenosines at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
| 2003 | Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
| 2007 | Design, synthesis, and preliminary biological evaluation of a novel triazole analogue of ceramide | 이상국 | Article |
| 2005 | Development of potent and selective human A3 adenosine receptor agonists. | 정낙신; 이상국 | Article |
