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Showing results 26 to 55 of 219

Issue DateTitleAuthor(s)Type
2005D-4′-thioadenosine derivatives as highly potent and selective agonists at the human A3 adenosine receptor정낙신Conference Paper
2012Decreased expression of synapse-related genes and loss of synapses in major depressive disorder정낙신Article
2011Design and Stereoselective Synthesis of 3'-Aminoadenosine Derivatives as Potential A3 Adenosine Receptor Antagonists최문주Master's Thesis
2011Design and Synthesis of 2΄-Azido-2΄-deoxy-4΄-selenofuranosyl Pyrimidines As Potential Antiviral Agents최정희Master's Thesis
2004Design and synthesis of 3′-ureidoadenosine-5′-uronamides: Effects of the 3′-ureido group on binding to the A 3 adenosine receptor정낙신Article
2011Design and synthesis of 5 '-homo-4 '-fluoro-aristeromycin derivatives as potent antiviral agents정낙신; 최원준Meeting Abstract
2008Design and synthesis of 5''-iodoneplanocin a and its analogues as potential S-adenosylhomocysteine hydrolase inhibitor정낙신Article
2003Design and synthesis of A3 adenosine receptor ligands, 2′-fluoro analogues of Cl-IB-MECA정낙신Conference Paper
2003Design and synthesis of A3 adenosine receptor ligands, 3′-fluoro analogues of Cl-IB-MECA정낙신Conference Paper
2011Design and Synthesis of Base Modified Carbanucleosides as Potential Adenosine Receptor Ligands김경림Master's Thesis
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 Binding Affinity of Novel Adenosine Analogues as Potent Adenosine Receptor LigandsHou, XiyanDoctoral Thesis
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
2010Design, Synthesis, Anti-Hepatitis C Virus (HCV) Activity of 3΄-C-Substituted Purine and Pyrimidine Nucleosides김유민Master's Thesis

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