2005 | Synthesis of 3'-ureidoadenosines and their high binding affinity at the mutant A3 adenosine receptor. | 이강만; 정낙신 | Article |
2005 | Synthesis of benzo[b]naphtho[2,3-d]thiophene-6,11-diones via palladium(II) acetate-mediated cyclization of 3-arylthio-1,4-naphthoquinone | 유충규 | Article |
2005 | Synthesis of homo-N-nucleoside with 1,2,4-triazole-3-carboxamide | 정낙신 | Conference Paper |
2005 | Synthesis and biological evaluation of quinoxaline-5,8-diones that inhibit vascular smooth muscle cell proliferation | 유충규; 이상국 | Article |
2005 | Synthesis of novel apio carbocyclic nucleoside analogues as selective A3 adenosine receptor agonists | 이강만; 정낙신 | Article |
2005 | Development of potent and selective human A3 adenosine receptor agonists. | 정낙신; 이상국 | Article |
2005 | Homology modeling and docking study of translationally controlled tumor proteins | 김춘미 | Meeting Abstract |
2005 | Molecular recognition of 3 '-modified adenosine neoligands to the human A3 adenosine receptor and its neoceptor. | 정낙신 | Meeting Abstract |
2005 | Synthesis and anti-tumor activity of fluorocyclopentenyl-pyrimidines | 정낙신 | Meeting Abstract |
2005 | Synthesis and antifungal activity of 5-arylamino-4,7-dioxobenzo[b] thiophenes | 유충규 | Article |
2005 | Synthesis and binding affinity of 3'-ureidoadenosine analogues at the A3 adenosine receptor. | 정낙신 | Meeting Abstract |
2005 | Synthesis and antifungal activity of naphthalene-1,4-diones modified at positions 2, 3, and 5 | 유충규 | Article |
2005 | Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-uronamides as human A3 adenosine receptor agonists | 정낙신; 이상국 | Meeting Abstract |
2005 | Synthesis and antifungal activity of 2/3-arylthio- and 2,3-bis(arylthio)-5- hydroxy-/5-methoxy-1,4-naphthoquinones | 유충규 | Article |
2005 | Antibacterial and antifungal activity of pinosylvin, a constituent of pine | 이강만; 이상국 | Article |
2005 | Synthesis and antifungal activity of noble 5-arylamino- and 6-arylthio-4,7-dioxobenzoselenazoles | 유충규 | Article |
2005 | Antiplatelet activity of J78 (2-chloro-3-[2′-bromo, 4′-fluoro-phenyl]-amino-8-hydroxy-1,4-naphthoquinone), an antithrombotic agent, is mediated by thromboxane (TX) A2 receptor blockade with TXA2 synthase inhibition and suppression of cytosolic Ca2+ mobilization | 유충규 | Article |
2005 | Biological properties of 2′-[18F]fluoroflumazenil for central benzodiazepine receptor imaging | 이승진 | Article |
2005 | In vitro degradation behavior of electrospun polyglycolide, polylactide, and poly(lactide-co-glycolide) | 이승진 | Article |
2005 | Preparation of 18F-human serum albumin: A simple and efficient protein labeling method with 18F using a hydrazone-formation method | 이승진 | Article |