2005 | Antibacterial and antifungal activity of pinosylvin, a constituent of pine | 이강만; 이상국 | Article |
2007 | Asymmetric synthesis of cyclopropyl-fused 2′-C-methylcarbanucleosides as potential anti-HCV agents | 이강만; 이승진; 신윤용; 정낙신 | Article |
2007 | Asymmetric synthesis of homo-apioneplanocin A as a potential S-adenosylhomocysteine hydrolase inhibitor | 이강만; 정낙신 | Meeting Abstract |
2006 | Asymmetric synthesis of homo-apioneplanocin A from d-ribose | 이강만; 정낙신 | Article |
2007 | Asymmetric synthesis of novel apio carbocyclic nucleoside analogues as potential antiviral and antitumor agent | 이강만; 정낙신 | Conference Paper |
2003 | Characteristics of chitosanases from Aspergillus fumigatus KB-1. | 이강만 | Article |
2005 | Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines. | 이강만; 정낙신; 이상국; 최원준 | Article |
2003 | Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
2007 | Design, 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 hydrolase | 이강만; 정낙신; 최선 | Meeting Abstract |
2007 | Design, 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 hydrolase | 이강만; 정낙신; 최선 | Article |
1992 | Determination of the pKa for histidine-51 residue in the ternary complex of horse liver alcohol dehydrogenase | 이강만 | Article |
1997 | I269S mutation in horse liver alcohol dehydrogenase S isoenzyme and its reactivity for steroids and retinoids | 이강만 | Article |
2000 | Identification of the self-interaction of rat TCTP/IgE-dependent histamine-releasing factor using yeast two-hybrid system | 이강만; 이경림; 윤태숙 | Article |
2000 | Isolation and characterization of chitosanase-producing microorganism, Aureobacterium sp. YL, from crab shells | 이강만 | Article |
2004 | Preparative and stereoselective synthesis of the versatile intermediate D-cyclopentenone with 4-hydroxymethyl substituent for the synthesis of carbocyclic nucleosides | 이강만; 정낙신 | Meeting Abstract |
1999 | Purification and characterization of a chitinase from Cytophaga sp. HJ isolated from sea sand | 이강만 | Article |
2005 | Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides | 이강만; 신윤용; 정낙신 | Conference Paper |
2002 | Stereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase inhibitor | 이강만; 정낙신 | Article |
2007 | Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신 | Conference Paper |
2005 | Structure-activity relationship of 5′-substituted fluoro-neplanocin A analogues as potent inhibitors of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Conference Paper |
1990 | Studies on the alkalophilic bacteria producing alkaline protease and its enzyme activities | 이강만 | Article |
1993 | Substitution of Gly-224 residue to Ile in yeast alcohol dehydrogenase and enzyme reaction mechanism | 이강만 | Article |
2007 | Synthesis and anti-HCV activity of 2′-β-hydroxymethylated nucleosides | 이강만; 정낙신 | Conference Paper |
2007 | Synthesis and biological activity of truncated fluorocyclopentenyl-nucleosides | 이강만; 정낙신; 이상국 | Meeting Abstract |
2006 | Synthesis of 2-C-hydroxymethylribofuranosylpurines as potent anti-hepatitis C virus (HCV) agents | 이강만; 정낙신 | Article |
2005 | Synthesis of 3'-ureidoadenosines and their high binding affinity at the mutant A3 adenosine receptor. | 이강만; 정낙신 | Article |
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 |
2004 | Synthesis of fluorinated cyclopentenyladenine as potent inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신 | Article |
2005 | Synthesis of novel apio carbocyclic nucleoside analogues as selective A3 adenosine receptor agonists | 이강만; 정낙신 | Article |
1991 | The conversion of lithocholic acid into 5β-androstan-3,17-dione in the cell-free system of Mycobacterium sp. NRRL B-3805 | 이강만 | Article |