Browsing "약학대학" byAuthorLee H.W.

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Showing results 1 to 30 of 37

Issue DateTitleAuthor(s)Type
2010A new DNA building block, 4′-selenothymidine: Synthesis and modification to 4′-seleno-AZT as a potential anti-HIV agent정낙신; 최원준Article
2011A3 adenosine receptor agonist reduces brain ischemic injury and inhibits inflammatory cell migration in rats정낙신Article
2007Alternative and improved syntheses of highly potent and selective A 3 adenosine receptor agonists, CI-IB-MECA and thio-CI-IB-MECA정낙신Article
2013C-Cbl-Mediated Neddylation Antagonizes Ubiquitination and Degradation of the TGF-β Type II Receptor정낙신; 이혁우Article
2006Conversion of A3 adenosine receptor agonists into selective antagonists by modification of the 5′-ribofuran-uronamide moiety정낙신Article
2005D-4′-thioadenosine derivatives as highly potent and selective agonists at the human A3 adenosine receptor정낙신Conference Paper
2009Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists정낙신; 최원준Article
2007Design, synthesis, and anti-tumor activity of 4′-thionucleosides as potent and selective agonists at the human A3 adenosine receptor정낙신; 이상국Article
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
2005Development of potent and selective human A3 adenosine receptor agonists.정낙신; 이상국Article
2012Fluorocyclopentenyl-cytosine with broad spectrum and potent antitumor activity정낙신; 최원준Article
2012Improved synthesis of a DNA-dependent protein kinase inhibitor IC86621정낙신Article
2017N6-Substituted 5′-N-Methylcarbamoyl-4′-selenoadenosines as Potent and Selective A3 Adenosine Receptor Agonists with Unusual Sugar Puckering and Nucleobase Orientation최선Article
2013Neddylation pathway regulates the proliferation and survival of macrophages정낙신Article
2013New RNA purine building blocks, 4'-selenopurine nucleosides: First synthesis and unusual mixture of sugar puckerings정낙신; 최원준Article
2014Overactivated neddylation pathway as a therapeutic target in lung cancer정낙신Article
2011Regio- and stereoselective synthesis of truncated 3′- aminocarbanucleosides and their binding affinity at the A 3 adenosine receptor정낙신; 최원준Article
2012Stereoselective synthesis and anti-HCV activity of conformationally restricted 2′-C-substituted carbanucleosides정낙신; 최원준Article
2007Stereoselective synthesis of 1′-functionalized-4′- thionucleosides정낙신Article
2007Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase이강만; 정낙신Conference Paper
2011Stereoselective synthesis of MLN4924, an inhibitor of NEDD8-activating enzyme정낙신; 최원준Article
2006Structure-activity relationships of 2-chloro-N6-substituted- 4′-thioadenosine-5′-uronamides as highly potent and selective agonists at the human A3 adenosine receptor정낙신; 이상국Article
2008Structure-activity relationships of 2-chloro-N6-substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as human A3 adenosine receptor antagonists정낙신; 최원준Article
2014Structure-activity relationships of 2′-modified-4′- selenoarabinofuranosyl-pyrimidines as anticancer agents정낙신Article
2023Structure-Activity Relationships of Truncated 1′-Homologated Carbaadenosine Derivatives as New PPARγ/δ Ligands: A Study on Sugar Puckering Affecting Binding to PPARs최선Article
2012Structure-activity relationships of truncated C2- or C8-substituted adenosine derivatives as dual acting A 2A and A 3 adenosine receptor ligands정낙신; 최선; 최원준Article
2011Suppression of inflammation response by a novel A 3 adenosine receptor agonist thio-Cl-IB-MECA through inhibition of Akt and NF-κB signaling정낙신; 이혁우Article
2010Synthesis and anti-hepatitis C virus (HCV) activity of 3′-C- substituted-methyl pyrimidine and purine nucleosides정낙신; 최원준Article
2011Synthesis and binding affinity of homologated adenosine analogues as A3 adenosine receptor ligands정낙신; 최원준Article

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