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Showing results 1 to 30 of 191

Issue DateTitleAuthor(s)Type
2000A highly efficient synthesis of L-β-2′-deoxy-4′-thio-1′-purine nucleosides as potential antiviral agents김길수; 정낙신Article
2005A highly efficient synthesis of unnatural L-sugars from D-ribose정낙신; 최원준Article
2010A new DNA building block, 4′-selenothymidine: Synthesis and modification to 4′-seleno-AZT as a potential anti-HIV agent정낙신; 최원준Article
1998A short and efficient synthesis of L-thioarbinose derivative: A versatile synthon for the synthesis of l-2'-deoxy-2',2'-disubstituted-4'- thionucleosides정낙신Article
2002A short and efficient synthetic approach to hydroxy (E)-stilbenoids via solid-phase cross metathesis정낙신Article
2012A straightforward synthesis of K-7174, a GATA-specific inhibitor정낙신Article
2011A3 adenosine receptor agonist reduces brain ischemic injury and inhibits inflammatory cell migration in rats정낙신Article
2010A3 adenosine receptor antagonist, truncated thio-Cl-IB-MECA, induces apoptosis in T24 human bladder cancer cells정낙신; 최원준Article
2007Alternative and improved syntheses of highly potent and selective A 3 adenosine receptor agonists, CI-IB-MECA and thio-CI-IB-MECA정낙신Article
2007Asymmetric synthesis and anti-RNA virus activity of cyclopropyl-fused 2 '-C-methyl-carbocyclic nucleosides정낙신; 장준Meeting Abstract
2007Asymmetric synthesis and biological activity of l-bicyclocarba-d4T정낙신Article
2012Asymmetric Synthesis of 6′-Fluoroaristeromycin Analogues as Potential S-Adenosylhomocysteine Hydrolase Inhibitor엄윤진Master's Thesis
2007Asymmetric synthesis of apio fluoroneplanocin a analogs as potential AdoHcy hydrolase inhibitor정낙신Article
2007Asymmetric synthesis of cyclopropyl-fused 2′-C-methylcarbanucleosides as potential anti-HCV agents이강만; 이승진; 신윤용; 정낙신Article
2007Asymmetric synthesis of homo-apioneplanocin A as a potential S-adenosylhomocysteine hydrolase inhibitor이강만; 정낙신Meeting Abstract
2007Asymmetric synthesis of novel apio carbocyclic nucleoside analogues as potential antiviral and antitumor agent이강만; 정낙신Conference Paper
2007Asymmetric synthesis of novel pseudo-D-vinylcyclopropyl nucleosides bearing quaternary carbon as potential anti-herpesvirus agent정낙신Article
2001Asymmetric synthesis of the versatile intermediates for the synthesis of D- and L-carbocyclic nucleosides.정낙신Meeting Abstract
2013C-Cbl-Mediated Neddylation Antagonizes Ubiquitination and Degradation of the TGF-β Type II Receptor정낙신; 이혁우Article
1998Carbocyclic analogues of the potent cytidine deaminase inhibitor 1-(β- D-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine)정낙신Article
1997Conformational analysis of the complete series of 2' and 3' monofluorinated dideoxyuridines정낙신Article
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
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

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