S. Chung

发表

2,3-diarylpyran-4-ones: a new series of selective cyclooxygenase-2 inhibitors.

M. Noh, K. Lim, J. Ha, 2004, Bioorganic & medicinal chemistry letters.

Injectable COX-2 inhibitor for postoperative pains

S. Chung, 2006 .

Structure‐Activity Relationship of 4,6‐Disubstituted Pyrimidines as EGFR and VEGFR‐2 Tyrosine Kinase Inhibitors

Jiho Song, K. Min, J. Lee, 2017 .

2,3-Diarylbenzopyran derivatives as a novel class of selective cyclooxygenase-2 inhibitors.

M. Noh, Shin Chung, Yung Hyup Hyup, 2003, Bioorganic & medicinal chemistry letters.

Additional flexibility solves the leaving group problem in cyclodextrin acylation

R. Breslow, S. Chung, 1990 .

In vitro structure-activity relationship and in vivo studies for a novel class of cyclooxygenase-2 inhibitors: 5-aryl-2,2-dialkyl-4-phenyl-3(2H)furanone derivatives.

Young Hoon Choi, Jin Kwan Kim, Ki-Wha Lee, 2004, Journal of medicinal chemistry.

A facile one-pot synthesis of 4,5-diaryl-2,2-dimethyl-3(2H)-furanones.

Jin Kwan Kim, S. Shin, Yeonjoon Kim, 2002, Bioorganic & medicinal chemistry.

Strong binding of ditopic substrates by a doubly linked occlusive C1 clamshell as distinguished from an aversive C2 loveseat cyclodextrin dimer

Ronald Breslow, R. Breslow, Shin Chung, 1990 .

HIGHLY POTENT AND SELECTIVE INHIBITORS OF ENDOTHELIN CONVERTING ENZYME

A. Stamford, M. Czarniecki, B. Mckittrick, 1996 .

Profiles of COX-2 inhibitors: present and future

S. Shin, K. Lim, S. Chung, 2005 .

A novel synthesis of substituted imidazoles, and a reexamination of a purported chymotrypsin model

Ronald Breslow, R. Breslow, Shin Chung, 1989 .

Metal-ion-catalyzed hydrolysis of monomethyl and dimethyl esters of 3-(2-imidazoleazo)phthalic acid: Bifunctional catalysis by carboxyl group and the metal ion in the hydrolysis of an alkyl ester

S. H. Lee, J. Suh, S. Chung, 1987 .

The Propionyl Ester of Lovastatin Decreases the Levels of Very Long Chain Fatty Acids in Fibroblasts Derived from Patients with X-linked Adrenoleukodystrophy

Dong-Wook Kim, Jiho Jang, Jiho Song, 2018, Bulletin of the Korean Chemical Society.

A Novel Synthesis of Substituted Imidazoles, and a Reexamination of a Purported Chymotrypsin Model.

R. Breslow, S. Chung, 1990 .

Non-steady-state kinetics for the carboxypeptidase A-catalyzed hydrolysis of O-[trans-(α-benzoylamino)cinnamoyl]-l-mandelate: Evidence for the productive nature of the accumulating intermediate

J. Suh, S. Chung, Gil-Bae Choi, 1989 .

Carboxypeptidase A-catalyzed hydrolysis of α-(acylamino)cinnamoyl derivatives of L-β-phenyllactate and L-phenylalaninate: evidence for acyl-enzyme intermediates

Junghun Suh, Wonhwa Cho, J. Suh, 1985 .

Synthesis and anti-tumor activity of imidazopyrazines as TAK1 inhibitors.

K. Min, S. Jang, Y. H. Kim, 2019, European journal of medicinal chemistry.

COX-2 inhibitors with a methylsulfoxide pharmacophore

S. Chung, 2005 .

A prodrug approach to COX-2 inhibitors with methylsulfone.

S. Shin, Jin Kyu Choi, J. Moh, 2004, Bioorganic & medicinal chemistry letters.

Structure-activity relationship of 7-aryl-2-anilino-pyrrolopyrimidines as Mer and Axl tyrosine kinase inhibitors

Jiho Song, K. Min, Jiwon Park, 2020, Journal of enzyme inhibition and medicinal chemistry.