2006 | Structure-activity relationships of 2-chloro-N6-substituted- 4′-thioadenosine-5′-uronamides as highly potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
2001 | Structure-activity relationships of apio nucleosides as potential antiviral agents | 정낙신 | Conference Paper |
1997 | Syntheses and antiviral activities of 1,3-dioxolanyl-, 1,3-oxathiolanyl- and 1,3-dithiolanylnucleosides with 2-hydroxymethyl substituents | 정낙신 | Article |
2007 | Synthesis and antitumor activity of fluorocyclopentenyl-pyrimidines | 정낙신; 이상국 | Conference Paper |
1999 | Synthesis and antiviral activities of 1,3-oxathiolanyl nucleosides with 5-hydroxymethyl substituent | 정낙신 | Conference Paper |
1998 | Synthesis and antiviral activity of 2′-fluorohexopyranosyl nucleosides | 정낙신 | Article |
1998 | Synthesis and antiviral activity of apio dideoxy nucleosides with azido or amino substituent | 정낙신 | Article |
2001 | Synthesis and antiviral activity of D- and L-2′-azido-2′,3′-dideoxy-4′-thiopyrimidine and purine nucleosides | 정낙신 | Conference Paper |
1999 | Synthesis and antiviral activity of D- and L-isodideoxy nucleosides with exocyclic methylene | 정낙신 | Conference Paper |
1999 | Synthesis and antiviral activity of L-2'-deoxy-2'-up-fluoro-4'- thionucleosides | 정낙신 | Conference Paper |
2003 | Synthesis and biological evaluation of halo-neplanocin A as novel mechanism-based inhibitors of S-Adenosylhomocysteine hydrolase | 정낙신 | Conference Paper |
2004 | Synthesis and biological evaluation of novel apio nucleosides with thiazole-4-carboxamide and 1,2,4-triazole-3-carboxamide | 정낙신; 이상국 | Article |
2004 | Synthesis and biological evaluation of novel tert-azido or ten-amino substituted penciclovir analogs | 정낙신; 김대기 | Article |
2002 | Synthesis and biological evaluation of novel thioapio dideoxynucleosides | 정낙신; 이상국; 최원준 | Article |
2003 | Synthesis and biological evaluation of pyrimidine nucleosides fused with 3′,4′-tetrahydrofuran ring | 정낙신 | Conference Paper |
2003 | Synthesis and biological evaluation of thymine nucleosides fused with 3′,4′-tetrahydrofuran ring | 정낙신 | Article |
2000 | Synthesis of (-)-Neplanocin A Analogues as Potential Antiviral Agents | 정낙신 | Article |
2003 | Synthesis of (Z)-(1-fluoro-2-hydroxymethyl-cyclopropylmethyl)purines | 정낙신 | Conference Paper |
2003 | Synthesis of 2-(3′-Azido- and 3′-Amino-3′-deoxy-β -D-ribofuranosyl)thiazole-4-carboxamide | 정낙신 | Article |
2005 | Synthesis of 3'-ureidoadenosines and their high binding affinity at the mutant A3 adenosine receptor. | 이강만; 정낙신 | Article |
2008 | Synthesis of 3′-acetamidoadenosine derivatives as potential A 3 adenosine receptor agonists | 정낙신; 최원준 | Article |
2005 | Synthesis of 3′-deoxy-3′-C-hydroxymethyl analogues of tiazofurin and ribavirin | 정낙신 | Conference Paper |
2005 | Synthesis of 3′-ureidoadenosine analogues and their binding affinity to the A3 adenosine receptor | 정낙신 | Conference Paper |
2003 | Synthesis of 5-Azacytidine nucleosides with rigid sugar moiety as potential antitumor agents | 정낙신 | Conference Paper |
2004 | Synthesis of 5′-substituted fluoro-neplanocin A analogues: Importance of a hydrogen bonding donor at 5′-position for the inhibitory activity of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
2003 | Synthesis of [1′-fluoro-2′,2′ -bis-(hydroxymethyl)-cyclopropylmethyl]purines as antiviral agents | 정낙신 | Conference Paper |
1999 | Synthesis of cyclopropyl-fused carbocyclic nucleosides via the regioselective opening of cyclicsulfi sulfites | 정낙신 | Article |
2004 | Synthesis of D- and L-apio nucleoside analogues with 2′-hydroxyl group as potential anti-HIV agents | 정낙신; 김대기 | Article |
2007 | Synthesis of enantiopure pseudo-L-vinylcyclopropyl nucleosides bearing quaternary carbon as potential anti-herpesvirus agent | 정낙신 | Article |
2004 | Synthesis of fluorinated cyclopentenyladenine as potent inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신 | Article |