D. H. Kim

发表

Insight into the stereochemistry in the inhibition of carboxypeptidase A with N-(hydroxyaminocarbonyl)phenylalanine: binding modes of an enantiomeric pair of the inhibitor to carboxypeptidase A.

Sang J. Chung, B. Oh, N. Ha, 2002, Bioorganic & medicinal chemistry.

Inhibition of Carboxypeptidase A with $\beta$ -Lactone-bearing phenylalanine. Design, Synthesis, and Stereochemistry-dependent Inhibition Mode

Mijoon Lee, D. H. Kim, 2001 .

Synthesis of 5,6,8,9,14,14a-hexahydroisoquino[1,2-b][3]benzazepines

D. H. Kim, 1992 .

Inactivation of a prototypic zinc-containing protease with (s)-2-benzyl-2-(3-oxo-2-isoxazolidinyl)acetic acid

D. H. Kim, Kyungeon Lee, 1996 .

A Method for Screening Enzyme Inhibitors Using Size Exclusion Chromatography and ESI-LC-MS/MS

R. Hartmann, S. Mathur, D. H. Kim, 2005, Journal of biomolecular screening.

Electrospray ionization mass spectrometric analysis for interaction of α-chymotrypsin with bebame, an active-site directed enzyme inhibitor

J. Hahn, D. H. Kim, Yeoun Jin Kim, 1996 .

Aromatic-aromatic ring interaction revisited with model compounds of Wilcox.

Kwang S. Kim, T. Ren, Yonghao Jin, 1997, Journal of biomolecular structure & dynamics.

Hippuryl-α-methylphenylalanine and hippuryl-α-methylphenyllactic acid as substrates for carboxypeptidase A. Syntheses, kinetic evaluation and mechanistic implication

Mijoon Lee, D. H. Kim, 2000 .

4'-bromo-5,6,7-trimethoxyflavone represses lipopolysaccharide-induced iNOS and COX-2 expressions by suppressing the NF-κB signaling pathway in RAW 264.7 macrophages.

Kyung-Tae Lee, Ji-Sun Shin, Yong Sup Lee, 2012, Bioorganic & medicinal chemistry letters.

Reversed hydroxamate-bearing thermolysin inhibitors mimic a high-energy intermediate along the enzyme-catalyzed proteolytic reaction pathway.

D. H. Kim, Jung Dae Park, 2003, Bioorganic & medicinal chemistry letters.

Cleavage of beta-lactone ring by serine protease. Mechanistic implications.

Sang J. Chung, D. H. Kim, Jung Dae Park, 2002, Bioorganic & medicinal chemistry.

Ring closure reaction of 4-(2-hydroxyanilino)-2-phenyl-5-pyrimidinecarboxylic acid with acetic anhydride. Synthesis of pyrimido[5,4-c] [1,5]benzoxazepin-5(11H)ones

A. A. Santilli, D. H. Kim, R. A. Fieber, 1972 .

Convenient synthesis of 6-substituted-2-chloro-5,12-dihydro-5-oxobenzoxazolo[3,2-a]quinolines and N-acylated-3-chlorodibenz[b,e][1,4]oxazepin-11(5H)-ones

Sang J. Chung, D. H. Kim, K. Joo, 1997 .

Thieno[2,3‐d]pyrimidines. I. A new method for the preparation of esters and amides of thieno[2,3‐d] pyrimidine‐6‐carboxylic acids

A. A. Santilli, D. H. Kim, S. Wanser, 1971 .

Acetic anhydride as a synthetic reagent

D. H. Kim, 1976 .

Improved syntheses of 1,4‐benzodiazepine‐2,5‐diones

D. H. Kim, 1975 .

Rearrangements of 4‐(2‐Aminophenyl)‐1,4‐dihydro‐2,6‐dimethyl‐3,5‐pyridinedicarboxylic acid diethyl ester

D. H. Kim, 1986 .

Convenient synthesis of optically pure α-mono and α, α-disubstituted β-amino acids

D. H. Kim, Jung Dae Park, H. Lee, 2003 .

Synthesis of 3-fluoro-2-substituted amino-5,12-dihydro-5-oxobenzoxazolo[3,2-a]quinoline-6-carboxylic acids employing the tandem double ring closure reaction of N-acetyl-N-(2-hydroxyphenyl)anthranilic acid as the key step

Sang J. Chung, D. H. Kim, 1995 .

Cysteine derivatives as inhibitors for carboxypeptidase A: synthesis and structure-activity relationships.

D. H. Kim, Jung Dae Park, 2002, Journal of medicinal chemistry.

Cleavage of β-lactone ring by serine protease. Mechanistic implications

Sang J. Chung, D. H. Kim, Jung Dae Park, 2002 .

Sulfamide derivatives as transition state analogue inhibitors for carboxypeptidase A.

D. H. Kim, Jung Dae Park, 2004, Bioorganic & medicinal chemistry.

Synthesis of naproxen via regioselective ring opening of (2S,3S)-epoxy-1-butanol

K. Ahn, D. H. Kim, J. S. Kim, 1993 .

Alpha-alkylcysteines as Inhibitors for Carboxypeptidase A. Synthesis, Evaluation, and Implication for Inhibitor Design Strategy

D. H. Kim, H. Lee, 2002 .

INACTIVATION OF CARBOXYPEPTIDASE A BY 2-BENZYL-3,4-EPITHIOBUTANOIC ACID

Sang J. Chung, D. H. Kim, 1995 .

Inhibitory stereochemistry of N-chloroacetyl-N-hydroxyleucine methyl ester for thermolysin

Yonghao Jin, D. H. Kim, 1996 .

Synthesis of 1,2,3,4,8,9,10,11‐octahydro‐[1,4] diazepino[6,5,4‐jk ]earbazole and related compounds

D. H. Kim, 1976 .

Regioselective Oxirane Ring Opening of trans-2,3-Epoxy Alcohols with Arylaluminum Complexes

K. Ahn, D. H. Kim, J. Kim, 1992 .

Sulfamide-based inhibitors for carboxypeptidase A. Novel type transition state analogue inhibitors for zinc proteases.

S. Ryu, D. H. Kim, J. Woo, 2002, Journal of Medicinal Chemistry.

Pyrrolo[2,3-d] pyrimidines. I. 5-hydroxypyrrolo[2,3-d] pyrimidines

A. A. Santilli, D. H. Kim, 1969 .

A Practical Method for the Conversion of β-Hydroxy Carboxylic Acids into the Corresponding β-Amino Acids

Yonghao Jin, D. H. Kim, 1998 .

Inhibition of Invasion and Capillary-like Tube Formation by Retrohydroxamate-based MMP Inhibitors

Seongshick Ryu, D. H. Kim, Seung-Taek Lee, 2011 .

Synthesis and evaluation of α, α-disubstituted-3-mercaptopropanoic acids as inhibitors for carboxypeptidase A and implications with respect to enzyme inhibitor design

D. H. Kim, Hyun-shin Lee, 2003 .

Synthesis of pyrimido[4,5-e][1,4]oxazepin-5-ones

A. A. Santilli, D. H. Kim, S. Wanser, 1972 .

Synthesis of 5-substituted-7-methoxy-2-phenylpyrimido[4,5-b]quinolines new synthesis of pyrimido[4,5-b]quinolines

A. A. Santilli, D. H. Kim, 1975 .

Synthesis of 4‐Aryl‐1,4‐dihydro‐2,6‐bis(trifluoromethyl)‐3,5‐pyridinedicarboxylates

D. H. Kim, 1986 .

Syntheses and kinetic evaluation of racemic and optically active 2-benzyl-2-methyl-3,4-epoxybutanoic acids as irreversible inactivators for carboxypeptidase A.

Mijoon Lee, D. H. Kim, 2002, Bioorganic & medicinal chemistry.

Synthesis and Cytotoxic Effects of Sulfonamide-Substituted 5,6,7-Trimethoxyflavones on Human Cancer Cell Lines

Kyung-Tae Lee, Yong Sup Lee, D. H. Kim, 2013 .

The chemistry of 5H‐benzoxazolo[3,2‐a]quinolin‐5‐ones. 5H‐Benzoxazolo[3,2‐a]quinolin‐5‐ones as synthons for the preparation of novel quinoline derivatives

D. H. Kim, 1981 .

Glucose-containing flavones--their synthesis and antioxidant and neuroprotective activities.

Yong Sup Lee, D. H. Kim, C. N. Naveen Kumar, 2009, Bioorganic & medicinal chemistry letters.

Optically active 2-benzyl-3-methanesulfinylpropanoic acid: Synthesis and evaluation as inhibitors for carboxypeptidase A.

D. H. Kim, G. Tian, Jing-Yi Jin, 2003, Bioorganic & medicinal chemistry.

(3R, 4S)-3-Benzyl-4-bromomethyloxetan-2-one, a fast acting alternate substrate inhibitor of α-chymotrypsin

D. H. Kim, J. Ryoo, 1995 .

Stereochemistry in inactivation of carboxypeptidase A. : structural analysis of the inactivated carboxypeptidase A by an enantiomeric pair of 2-benzyl-3,4-epoxybutanoic acids

S. Ryu, Hee‐Jeong Choi, D. H. Kim, 1997 .