S. Cheon

发表

Semisynthesis of Licochalcone E and Biological Evaluation as Vasorelaxant Agents

M. Oak, Goo Yoon, Jung-Ok Lee, 2010 .

Design of novel agents for the therapy of non-insulin dependent diabetes mellitus (NIDDM)

J. Foley, L. Révész, P. Bell, 1993 .

5-HT2C receptor agonists with potential anorectic activity

Goo Yoon, S. Cheon, H. Jeong, 2008, Archives of pharmacal research.

Licochalcone E reduces chronic allergic contact dermatitis and inhibits IL-12p40 production through down-regulation of NF-kappa B.

Sung Ho Lee, Hyung-Seok Kim, B. Kang, 2010, International immunopharmacology.

Dual regulation of mast cell degranulation through IgE receptor-mediated modulation of M2-type pyruvate kinase

Kyeong-Man Kim, S. Cheon, D. Cho, 2014, Archives of pharmacal research.

Design and synthesis of 4-benzylpiperidine carboxamides as dual serotonin and norepinephrine reuptake inhibitors.

Kyeong-Man Kim, S. Paudel, S. Cheon, 2015, Bioorganic & medicinal chemistry.

Licochalcone E activates Nrf2/antioxidant response element signaling pathway in both neuronal and microglial cells: therapeutic relevance to neurodegenerative disease.

B. Kang, Young-Chang Cho, H. Choi, 2012, The Journal of nutritional biochemistry.

Selectivity of commonly used inhibitors of clathrin-mediated and caveolae-dependent endocytosis of G protein-coupled receptors.

S. Nah, Kyeong-Man Kim, M. Oak, 2015, Biochimica et biophysica acta.

Induction of apoptosis by the licochalcone E in endothelial cells via modulation of NF-kappaB and Bcl-2 Family.

J. Park, Nam-Ho Kim, B. Shin, 2007, Biological & pharmaceutical bulletin.

Licochalcone E has an antidiabetic effect.

Hong Gyu Park, G. Woo, E. Bak, 2012, The Journal of nutritional biochemistry.

Topoisomerase i inhibition and cytotoxicity of licochalcones A and E fromGlycyrrhiza inflata

B. Kang, Goo Yoon, S. Cheon, 2007, Archives of pharmacal research.

Synthesis of [guanido‐13C]‐γ‐hydroxyarginine

T. Zabriskie, Goo Yoon, S. Cheon, 2009 .

Agonist-induced changes in RalA activities allows the prediction of the endocytosis of G protein-coupled receptors.

Kyeong-Man Kim, M. Oak, S. Cheon, 2016, Biochimica et biophysica acta.

Substituted tetrahydropyrrolo[2,1-b]oxazol-5(6H)-ones and tetrahydropyrrolo[2,1-b]thiazol-5(6H)-ones as hypoglycemic agents.

J. Gao, R. Simpson, R. Deems, 1998, Journal of medicinal chemistry.

N-linked Glycosylation on the N-terminus of the dopamine D2 and D3 receptors determines receptor association with specific microdomains in the plasma membrane.

K. Kwon, C. Shin, Kyeong-Man Kim, 2015, Biochimica et biophysica acta.

Cytotoxic allyl retrochalcone from the roots of Glycyrrhiza inflata.

Y. Jung, Goo Yoon, S. Cheon, 2005, Chemical & pharmaceutical bulletin.

Design, synthesis, and biological evaluation of arylpiperazine-benzylpiperidines with dual serotonin and norepinephrine reuptake inhibitory activities.

Kyeong-Man Kim, S. Paudel, S. Cheon, 2016, Bioorganic & medicinal chemistry.

Palladium catalyzed double heck arylation of cyclopentene

J. Tomesch, M. Prashad, S. Cheon, 1989 .

A practical synthesis of trans-iodoolefins

W. Christ, Y. Kishi, Haolun Jin, 1986 .

Total synthesis of a fully protected palytoxin carboxylic acid

J. B. White, M. Martinelli, W. Christ, 1989 .

Total Synthesis of Palytoxin Carboxylic Acid and Palytoxin Amide

W. Christ, R. W. Armstrong, H. Fujioka, 1989 .

Synthesis and comparative molecular field analysis (CoMFA) of antitumor 3-arylisoquinoline derivatives.

W. Cho, S. Cheon, C. O. Lee, 1998, Bioorganic & medicinal chemistry.

Facile Synthesis of 5‐Substituted 1H‐Tetrazoles Catalyzed by Tetrabutylammonium Hydrogen Sulfate in Water

Zengtao Wang, S. Cheon, Zhiguo Liu, 2015 .

Antitumor activity of 5-aryl-2,3-dihydroimidazo[2,1-a]isoquinolines.

D. Handley, S. Cheon, V. Parrino, 1995, Journal of medicinal chemistry.

Studies on the synthesis andin vitro antitumor activity of the isoquinolone derivatives

J. Y. Lee, W. Cho, B. Choi, 1999, Archives of pharmacal research.

Structural modification of 5-aryl-2,3-dihydroimidazo[2,1-a]isoquinoline platelet activating factor receptor antagonists.

D. Handley, S. Cheon, V. Parrino, 1993, Journal of medicinal chemistry.

Total synthesis of 1-deoxygulonojirimycin. Revision of the absolute configuration of the natural product

W. Ham, S. Cheon, Jae-Eun Joo, 2005 .

Synthesis, biological evaluation, and molecular docking study of novel allyl-retrochalcones as a new class of protein tyrosine phosphatase 1B inhibitors.

Ying Su, Suqing Zheng, Weiwei Zhu, 2019, Bioorganic & medicinal chemistry.

Stereoselective total synthesis of (+)-licochalcone E

Zengtao Wang, Goo Yoon, S. Cheon, 2011, Archives of pharmacal research.

An enantioselective total synthesis of (S)-(−)-licochalcone E: determination of the absolute configuration

Goo Yoon, S. Cheon, Zhiguo Liu, 2010 .

A facile synthesis of (6 S ,1′ S )-(+)-hernandulcin and (6 S ,1′ R )-(+)-epihernandulcin

S. Cheon, H. Lim, Jung Hun Kim, 2003 .

Studies of structure activity relationship of flavonoids for the anti-allergic actions

S. Ryu, Kyeong-Man Kim, M. Oak, 1998, Archives of pharmacal research.

Synthesis of (+)-hernandulcin and (+)-epihernandulcin

S. Cheon, H. Lim, Jung Hun Kim, 2002 .

Design, synthesis and evaluation of 5-substituted 1-H-tetrazoles as potent anticonvulsant agents

Yi Jin, Changju Chun, Bangrong Cai, 2017, Archives of pharmacal research.

Design, synthesis and evaluation of 5-substituted 1-H-tetrazoles as potent anticonvulsant agents

Yi Jin, Bangrong Cai, Tiantian Wang, 2016, Archives of Pharmacal Research.

Synthesis of benzo[c]phenanthridine derivatives and theirin vitro antitumor activities

B. Kang, W. Cho, B. Choi, 1996 .

Total Synthesis of 1-Deoxygulonojirimycin. Revision of the Absolute Configuration of the Natural Product.

W. Ham, S. Cheon, Jae-Eun Joo, 2005 .

Base-catalyzed rearrangement of some 1,3-oxathiolane sulfoxides: Mechanistic viewpoint of the sigmatropic and elimination reactions

S. Cheon, H. Hahn, K. Nam, 2004 .

Exploration of substituted arylpiperazine-tetrazoles as promising dual norepinephrine and dopamine reuptake inhibitors.

Kyeong-Man Kim, S. Paudel, Goo Yoon, 2016, Bioorganic & medicinal chemistry.

Concise synthesis of licochalcone C and its regioisomer, licochalcone H

S. Paudel, Zengtao Wang, Goo Yoon, 2013, Archives of pharmacal research.

Synthesis and structure-activity relationship studies of 2,3-dihydroimidazo[2,1-a]isoquinoline analogs as antitumor agents

B. Kang, W. Cho, B. Choi, 1997, Archives of pharmacal research.

Palladium-Catalyzed Double Heck Arylation of Cyclopentene.

J. Tomesch, M. Prashad, S. Cheon, 1990 .

Design and synthesis of novel antidiabetic agents

Y. Pak, S. Cheon, H. Hahn, 2005, Archives of pharmacal research.

Design, synthesis and docking study of 5-(substituted benzylidene)thiazolidine-2,4-dione derivatives as inhibitors of protein tyrosine phosphatase 1B.

Su-Nam Kim, Zengtao Wang, Woojung Lee, 2014, Bioorganic & medicinal chemistry letters.

Synthesis and biological evaluation of 3-phenethylazetidine derivatives as triple reuptake inhibitors.

Kihang Choi, Minsoo Han, Chiman Song, 2014, Bioorganic & medicinal chemistry letters.

A Novel Partial PPARα/γ Dual Agonist SN159 Improves Insulin Sensitivity

Su-Nam Kim, Yong Kee Kim, Ki-Hyun Kim, 2016 .

Antidiabetic effect of SN158 through PPARα/γ dual activation in ob/ob mice.

G. Bae, Su-Nam Kim, Yong Kee Kim, 2017, Chemico-biological interactions.

Molecular Modeling of Licochalcone E as Protein Tyrosine Phosphatase 1B Inhibitor

Yong Cheol Kang, Cheolhee Kim, J. Shim, 2016 .

Short and Efficient Synthesis of Licochalcone B and D Through Acid-Mediated Claisen-Schmidt Condensation

S. Paudel, Zengtao Wang, Goo Yoon, 2013 .

Short and Efficient Synthesis of Licochalcone B (Ia) and D (Ib) Through Acid‐Mediated Claisen—Schmidt Condensation.

S. Paudel, Zengtao Wang, Goo Yoon, 2014 .

Design, synthesis, and evaluation of bromo-retrochalcone derivatives as protein tyrosine phosphatase 1B inhibitors.

Su-Nam Kim, Woojung Lee, Goo Yoon, 2011, Bioorganic & medicinal chemistry letters.

Structure-activity relationship studies of isoquinolinone type anticancer agent

Sang-Un Choi, W. Cho, B. Choi, 2001, Archives of pharmacal research.

Synthesis and structure-activity relationship studies of substituted isoquinoline analogs as antitumor agent

Sang-Un Choi, W. Cho, B. Choi, 1998, Archives of pharmacal research.

Synthesis of antineoplaston A10 analogs as potential antitumor agents

Sang-Un Choi, W. Cho, B. Choi, 1998, Archives of pharmacal research.

Design, synthesis and docking study of 4-arylpiperazine carboxamides as monoamine neurotransmitters reuptake inhibitors.

Kyeong-Man Kim, S. Paudel, Goo Yoon, 2018, Bioorganic & medicinal chemistry.

Inhibitory effect of chalcones and their derivatives from Glycyrrhiza inflata on protein tyrosine phosphatase 1B.

Su-Nam Kim, Woojung Lee, Goo Yoon, 2009, Bioorganic & Medicinal Chemistry Letters.

Design and Evaluation of Licochalcone A Derivatives as Anticancer Agents

J. Shim, Seung-Sik Cho, Goo Yoon, 2018 .

Concise synthesis of licochalcone C and its regioisomer, licochalcone H

S. Paudel, Zengtao Wang, Goo Yoon, 2013, Archives of Pharmacal Research.

Total Synthesis of Licochalcone E

Goo Yoon, S. Cheon, H. Jeong, 2009 .

Design, synthesis, and systematic evaluation of 4-arylpiperazine- and 4-benzylpiperidine napthyl ethers as inhibitors of monoamine neurotransmitters reuptake.

Kyeong-Man Kim, S. Paudel, Goo Yoon, 2018, Bioorganic & medicinal chemistry.

Triple reuptake inhibitors: Design, synthesis and structure-activity relationship of benzylpiperidine-tetrazoles.

Kyeong-Man Kim, S. Paudel, Goo Yoon, 2017, Bioorganic & medicinal chemistry.

Design, synthesis and in vitro activity of 1,4-disubstituted piperazines and piperidines as triple reuptake inhibitors.

Kyeong-Man Kim, S. Paudel, Goo Yoon, 2017, Bioorganic & medicinal chemistry.

Structural Requirements for Modulating 4-Benzylpiperidine Carboxamides from Serotonin/Norepinephrine Reuptake Inhibitors to Triple Reuptake Inhibitors

Kyeong-Man Kim, Eunae Kim, S. Paudel, 2021, Biomolecules & therapeutics.

Excavation of lead compounds that inhibit mast cell degranulation by combinatorial chemistry and activity-guided

Kyeong-Man Kim, M. Oak, H. Oh, 2004, Archives of pharmacal research.

Design, synthesis, and evaluation of bitopic arylpiperazine-phthalimides as selective dopamine D3 receptor agonists.

Zhengzhi Wu, S. Cheon, Yongkai Cao, 2018, MedChemComm.

Design, synthesis and evaluation of bitopic arylpiperazinephenyl-1,2,4-oxadiazoles as preferential dopamine D3 receptor ligands.

Kyeong-Man Kim, S. Cheon, C. Min, 2016, Bioorganic & medicinal chemistry.

Synthesis and evaluation of arylpiperazine-reverse amides as biased dopamine D3 receptor ligands.

Kyeong-Man Kim, S. Paudel, S. Cheon, 2015, Bioorganic & medicinal chemistry.