S. Kang

发表

Synthesis of 1,2,3-trisubstituted pyrrolo[3,2-c]quinolines via palladium-catalyzed heteroannulation with internal alkynes

Sang Sun Park, S. Kang, Sungsoo S. Kim, 1999 .

A FACILE METHOD FOR DIRECT CONVERSION OF DIHYDROFUROQUINOLONES TO DIHYDROPYRROLOQUINOLONES

H. Cheon, S. Kang, Sungsoo S. Kim, 1998 .

Synthesis and PTP1B inhibition of 1,2-naphthoquinone derivatives as potent anti-diabetic agents.

Sung Soo Kim, H. Cheon, Sung-Don Yang, 2002, Bioorganic & medicinal chemistry letters.

A novel 11β-HSD1 inhibitor improves diabesity and osteoblast differentiation.

S. B. Park, W. Jung, S. Rhee, 2014, Journal of molecular endocrinology.

Efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine

Jae Woo Park, Tae Yun Lee, T. Hong, 2019, Journal of Translational Medicine.

Efficient synthesis of 2-imidazol-2-ylacetates

J. Ahn, S. Kang, Joong-Kwon Choi, 2006 .

Protein Tyrosine Phosphatase 1B Inhibitors: Catechols

Sung Soo Kim, H. Cheon, Sung-Don Yang, 2003 .

Facile synthesis of benzo[4,5]furo[3,2-c]pyridines via palladium-catalyzed intramolecular Heck reaction

S. Kang, D. Ha, Su Jung Lee, 2009 .

Synthesis and SAR of Benzimidazole Derivatives Containing Oxycyclic Pyridine as a Gastric H+/K+‐ATPase Inhibitors.

H. Cheon, S. Kang, Sungsoo S. Kim, 2002 .

Synthesis and DP-IV inhibition of cyano-pyrazoline derivatives as potent anti-diabetic agents.

Sung Soo Kim, H. Cheon, S. Rhee, 2004, Bioorganic & medicinal chemistry letters.

SAR Study of β-Aminoacyl-Containing Cyclic Hydrazide Derivatives as DPP-IV Inhibitors

H. Cheon, S. Rhee, J. Ahn, 2008 .

Synthesis and biological evaluation of cyclic sulfamide derivatives as 11β-hydroxysteroid dehydrogenase 1 inhibitors.

W. Jung, J. Bok, S. Rhee, 2012, ACS medicinal chemistry letters.

Identification of cyclicsulfonamide derivatives with an acetamide group as 11β-hydroxysteroid dehydrogenase 1 inhibitors.

C. Kim, N. Kang, S. Rhee, 2011, Chemical & pharmaceutical bulletin.

Synthesis and 11β hydroxysteroid dehydrogenase 1 inhibition of thiazolidine derivatives with an adamantyl group.

C. Kim, W. Jung, M. Bae, 2011, Bioorganic & medicinal chemistry letters.

Discovery of cyclicsulfonamide derivatives as 11 beta-hydroxysteroid dehydrogenase 1 inhibitors.

C. Kim, H. Cheon, S. Rhee, 2010, Bioorganic & medicinal chemistry letters.

Optimization of Enzyme Activity Assay for Screening of Acryl CoA: Monoacylglycerol Acyltransferase 2 Inhibitors: Optimization of assay system for screening of MGAT2 inhibitors

W. Jung, S. Rhee, J. S. Park, 2015 .

Synthesis and biological evaluation of thiazole derivatives as GPR119 agonists.

W. Jung, S. Rhee, K. Jung, 2017, Bioorganic & medicinal chemistry letters.

Design, synthesis, and biological evaluation of aryl N-methoxyamide derivatives as GPR119 agonists.

S. Rhee, M. Bae, K. Jung, 2017, Bioorganic & medicinal chemistry letters.

Synthesis of tetrahydrocarbazole derivatives as potent β3-Adrenoceptor agonists

H. Cheon, S. Kang, Joong-Kwon Choi, 2004 .

Discovery of a new and efficient small molecule for neuronal differentiation from mesenchymal stem cell.

Sung Soo Kim, H. Jung, Sang-Un Choi, 2009, Journal of medicinal chemistry.

Synthesis and Biological Evaluation of Maleimide Derivatives for Neuronal Differentiation

N. Kang, M. Bae, J. Ahn, 2009 .

Synthesis and biological evaluation of rhodanine derivatives as PRL-3 inhibitors.

Suk-Kyeong Jung, D. Jeong, S. Ryu, 2006, Bioorganic & medicinal chemistry letters.

Synthesis, biological evaluation and structural determination of beta-aminoacyl-containing cyclic hydrazine derivatives as dipeptidyl peptidase IV (DPP-IV) inhibitors.

Jie-Oh Lee, S. Kim, Sung Soo Kim, 2007, Bioorganic & medicinal chemistry letters.

Regio- and stereoselective ring opening of vinyl epoxides with MgBr2

S. Kim, Sung Soo Kim, J. Ahn, 2004 .

Synthesis and biological evaluation of thienopyrimidine derivatives as GPR119 agonists.

W. Jung, S. Rhee, M. Bae, 2014, Bioorganic & medicinal chemistry letters.

Design and synthesis of novel epidermal growth factor receptor kinase inhibitors

C. Ahn, S. Kang, Joong-Kwon Choi, 2005 .

Indenone Derivatives: A Novel Template for Peroxisome Proliferator-Activated Receptor γ (PPARγ) Agonists

Seung Jun Kim, W. Jung, H. Cheon, 2006 .

PTP-1B inhibitors: cyclopenta[d][1,2]-oxazine derivatives.

S. Han, H. Cheon, S. Rhee, 2006, Bioorganic & medicinal chemistry letters.

Studies of rhodium-catalyzed ring opening of vinyl epoxides

J. Ahn, S. Kang, Joong-Kwon Choi, 2004 .

Synthesis and biological evaluation of pyrazoline analogues with beta-amino acyl group as dipeptidyl peptidase IV inhibitors.

Jie-Oh Lee, Sung Soo Kim, H. Cheon, 2008, European journal of medicinal chemistry.

Synthesis and biological evaluation of homopiperazine derivatives with beta-aminoacyl group as dipeptidyl peptidase IV inhibitors.

Jie-Oh Lee, Sung Soo Kim, H. Cheon, 2008, Bioorganic & medicinal chemistry letters.

Scandium(III) Triflate—TMSCl Promoted Cyclization of Aziridin-1-yl Oximes to 5,6-Dihydro-4H-[1,2,4]oxadiazines.

J. Ahn, S. Kang, Joong-Kwon Choi, 2007 .

Scandium(III) triflate–TMSCl promoted cyclization of aziridin-1-yl oximes to 5,6-dihydro-4H-[1,2,4]oxadiazines

J. Ahn, S. Kang, Joong-Kwon Choi, 2006 .

Facile Synthesis of Alkyl 1-Oxo-3-phenyl-1H-indene-2-carboxylate through Palladium-catalyzed Carboalkoxylation from 2-Bromo-3-phenylinden-1-ones

J. Ahn, S. Kang, Sungsoo S. Kim, 2008 .

Furo[3,2-h]quinoline Derivatives as a Gastric H + /K + -ATPase Inhibitors

H. Cheon, S. Kang, Sungsoo S. Kim, 2002 .

Synthesis of 4-Phenylamino-3-vinylquinoline Derivatives as Gastric H + /K + -ATPase Inhibitors

Sung Soo Kim, S. Kang, Joong-Kwon Choi, 2004 .

Anti-diabetic and anti-inflammatory effect of a novel selective 11β-HSD1 inhibitor in the diet-induced obese mice.

H. Jeong, S. B. Park, W. Jung, 2013, European journal of pharmacology.

Synthesis and structure-activity relationship of novel indene N-oxide derivatives as potent peroxisome proliferator activated receptor γ (PPARγ) agonists

H. Cheon, S. Rhee, J. Ahn, 2007 .

Anti-diabetic and anti-adipogenic effects of a novel selective 11β-hydroxysteroid dehydrogenase type 1 inhibitor, 2-(3-benzoyl)-4-hydroxy-1,1-dioxo-2H-1,2-benzothiazine-2-yl-1-phenylethanone (KR-66344).

W. Jung, H. Cheon, N. Kang, 2011, Biochemical pharmacology.

Anti-diabetic and anti-adipogenic effects of a novel selective 11β-hydroxysteroid dehydrogenase type 1 inhibitor in the diet-induced obese mice.

W. Jung, N. Kang, S. Rhee, 2012, European journal of pharmacology.

Discovery of β-aminoacyl containing thiazolidine derivatives as potent and selective dipeptidyl peptidase IV inhibitors.

Jie-Oh Lee, Sung Soo Kim, S. Schneider, 2011, Bioorganic & medicinal chemistry letters.

Suzuki reaction of cyclopenta[d][1,2]oxazine in aqueous solvent with water-soluble phosphine ligand

J. Ahn, S. Kang, Joong-Kwon Choi, 2006 .

Synthesis of 2-pyrazoline-5-carboxylic acid derivatives using trimethylsilyldiazomethane

Sung Soo Kim, D. K. An, J. Ahn, 2005 .

Synthesis of 2-Pyrazoline-5-carboxylic Acid Derivatives Using Trimethylsilyldiazomethane.

Sung Soo Kim, D. K. An, J. Ahn, 2005 .

Protein Tyrosine Phosphatase 1B Inhibitors: Heterocyclic Carboxylic Acids

H. Cheon, J. Ahn, S. Kang, 2003 .

Synthesis and biological evaluation of α-sulfonamido-N-adamantanecarboxamide derivatives as 11β-HSD1 inhibitors

S. Rhee, J. Ahn, S. Kang, 2015 .

Indenone derivatives: a novel template for peroxisome proliferator-activated receptor gamma (PPARgamma) agonists.

W. Jung, H. Cheon, S. Rhee, 2006, Journal of medicinal chemistry.

Regio‐ and Stereoselective Ring Opening of Vinyl Epoxides with MgBr2.

S. Kim, Sung Soo Kim, J. Ahn, 2004 .

Synthesis and pharmacological profile of 1-aryl-3-substituted pyrrolo[3,2-c]quinolines.

H. Cheon, S. Kang, Sungsoo S. Kim, 1999, Bioorganic & medicinal chemistry letters.