Browsing byAuthorChun M.W.

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Showing results 8 to 37 of 67

Issue DateTitleAuthor(s)Type
2005D-4′-thioadenosine derivatives as highly potent and selective agonists at the human A3 adenosine receptor정낙신Conference Paper
2004Design and synthesis of 3′-ureidoadenosine-5′-uronamides: Effects of the 3′-ureido group on binding to the A 3 adenosine receptor정낙신Article
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
2007Design, enantiopure synthesis, and biological evaluation of novel ISO-D-2′,3′-dideoxy-3′-fluorothianucleoside derivatives as a bioisostere of lamivudine정낙신Article
2003Design, synthesis and binding affinity of 3′-fluoro analogues of Cl-IB-MECA as adenosine A3 receptor ligands이승진; 정낙신Article
2007Design, synthesis, and anti-tumor activity of 4′-thionucleosides as potent and selective agonists at the human A3 adenosine receptor정낙신; 이상국Article
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
2005Development of potent and selective human A3 adenosine receptor agonists.정낙신; 이상국Article
2003N6-substituted D-4′-thioadenosine-5′-methyluronamides: Potent and selective agonists at the human A3 adenosine receptor정낙신Article
1998Participation of sulfur occurred during the Mitsunobu reaction: Synthesis of novel isodideoxythionucleosides정낙신Article
1998Ring contraction and rearrangement of 4-thiofuranose derivatives observed during dast fluorination in the synthesis of L-2'-'up'-fluoro-4'- thiothymidine정낙신Article
2007Stereoselective synthesis of 1′-functionalized-4′- thionucleosides정낙신Article
2005Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides이강만; 신윤용; 정낙신Conference Paper
2002Stereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase inhibitor이강만; 정낙신Article
2002Stereoselective synthesis of amino-substituted apio dideoxynucleosides through a distant neighboring group effect정낙신Article
2005Stereoselective synthesis of conformationally rigid apio carbanucleosides as potential antiviral agents정낙신Conference Paper
2007Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase이강만; 정낙신Conference Paper
2005Stereoselective synthesis of novel thioiso dideoxy nucleosides with exocyclic methylene as potential antiviral agents정낙신Conference Paper
2005Structure-activity relationship of 5′-substituted fluoro-neplanocin A analogues as potent inhibitors of S-adenosylhomocysteine hydrolase이강만; 정낙신; 이상국Conference Paper
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
2001Structure-activity relationships of apio nucleosides as potential antiviral agents정낙신Conference Paper
1997Syntheses and antiviral activities of 1,3-dioxolanyl-, 1,3-oxathiolanyl- and 1,3-dithiolanylnucleosides with 2-hydroxymethyl substituents정낙신Article
2007Synthesis and antitumor activity of fluorocyclopentenyl-pyrimidines정낙신; 이상국Conference Paper
1999Synthesis and antiviral activities of 1,3-oxathiolanyl nucleosides with 5-hydroxymethyl substituent정낙신Conference Paper
1998Synthesis and antiviral activity of 2′-fluorohexopyranosyl nucleosides정낙신Article
1998Synthesis and antiviral activity of apio dideoxy nucleosides with azido or amino substituent정낙신Article

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