Browsing "약학대학" byAuthor정낙신

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Showing results 31 to 60 of 205

Issue DateTitleAuthor(s)Type
2003Design and synthesis of A3 adenosine receptor ligands, 3′-fluoro analogues of Cl-IB-MECA정낙신Conference Paper
2009Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists정낙신; 최원준Article
2008Design and synthesis of novel 2′,3′-dideoxy-4′-selenonucleosides as potential antiviral agents정낙신; 최원준Article
2001Design and synthesis of novel fluorocyclopropanoid nucleosides정낙신Article; Proceedings Paper
2008Design and synthesis of truncated 4'-thioadenosine derivatives as potent and selective A3 adenosine receptor antagonists.정낙신; 최원준Article
2007Design, enantiopure synthesis, and biological evaluation of novel ISO-D-2′,3′-dideoxy-3′-fluorothianucleoside derivatives as a bioisostere of lamivudine정낙신Article
2011Design, synthesis and anticancer activity of novel dihydrobenzofuro[4,5-b] [1,8]naphthyridin-6-one derivatives정낙신Article
2003Design, synthesis and binding affinity of 3′-fluoro analogues of Cl-IB-MECA as adenosine A3 receptor ligands이승진; 정낙신Article
2011Design, Synthesis, and Anti-HCV Activity of 2 '-Modified-4 '-selenonucleosides정낙신; 최원준; 이혁우Meeting Abstract
2007Design, synthesis, and anti-tumor activity of 4′-thionucleosides as potent and selective agonists at the human A3 adenosine receptor정낙신; 이상국Article
2007Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines정낙신; 이상국Meeting Abstract
2005Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines.이강만; 정낙신; 이상국; 최원준Article
2010Design, synthesis, and binding of homologated truncated 4′-thioadenosine derivatives at the human A3 adenosine receptors정낙신; 최선; 최원준Article
2006Design, synthesis, and biological activity of N6-substituted-4′-thioadenosines at the human A3 adenosine receptor정낙신; 이상국Article
2003Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase이강만; 정낙신; 이상국Article
2007Design, synthesis, and biological evaluation of novel iso-d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives정낙신Article
2003Design, synthesis, and in vitro evaluation of APIO analogue of neplanocin A정낙신Conference Paper
2007Design, synthesis, and molecular modeling studies of 5'-deoxy-5'-ureidoadenosine: 5'-ureido group as a multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase이강만; 정낙신; 최선Meeting Abstract
2007Design, synthesis, and molecular modeling studies of 5′-deoxy-5′-ureidoadenosine: 5′-ureido group as multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase이강만; 정낙신; 최선Article
2009Design, synthesis, antitumor activity and mode of action of novel oxiranyl and thiiranyl phenol derivatives정낙신Article
2008Development of A3 adenosine receptor ligands.정낙신Article
2009Development of next generation 4'-selenonucleosides.정낙신Article
2007Development of novel clinical candidates targeting A(3) adenosine receptor정낙신Meeting Abstract
2005Development of potent and selective human A3 adenosine receptor agonists.정낙신; 이상국Article
2010Discovery of a new human A2A adenosine receptor agonist, truncated 2-hexynyl-4′-thioadenosine정낙신; 최선Article
2007Discovery of a new nucleoside template for human A3 adenosine receptor ligands: D-4′-thioadenosine derivatives without 4′-hydroxymethyl group as highly potent and selective antagonists정낙신; 이상국Article
2009Discovery of a new template for anticancer agents: 2′-deoxy-2′- fluoro-4′-selenoarabinofuranosyl-cytosine (2′-F-4′-seleno-ara- C)정낙신; 이상국; 최선; 최원준Article
2006Docking studies of agonists and antagonists suggest an activation pathway of the A3 adenosine receptor정낙신Article
2009Efficient and practical synthesis of l-hamamelose정낙신Article
2006Establishment of an assay for P2X7 receptor-mediated cell death정낙신Article

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