W. Cho

发表

Caveolin-1 inhibits matrix metalloproteinase-2 activity in the heart.

E. Daniel, A. El-Yazbi, W. Cho, 2007, Journal of molecular and cellular cardiology.

Development of kNN QSAR Models for 3-Arylisoquinoline Antitumor Agents

Alexander Golbraikh, Alexander Tropsha, A. Tropsha, 2011 .

Akt Cys-310-targeted Inhibition by Hydroxylated Benzene Derivatives Is Tightly Linked to Their Immunosuppressive Effects*

Ji Yeon Lee, M. Won, J. Y. Kim, 2010, The Journal of Biological Chemistry.

Design and synthesis of novel androgen receptor antagonists via molecular modeling.

W. Cho, Chao Zhao, You Hee Choi, 2016, Bioorganic & medicinal chemistry.

SAR based design of nicotinamides as a novel class of androgen receptor antagonists for prostate cancer.

Keesook Lee, W. Cho, Eunsook Park, 2013, Journal of medicinal chemistry.

A maresin 1/ROR&agr;/12-lipoxygenase autoregulatory circuit prevents inflammation and progression of nonalcoholic steatohepatitis

J. Cha, Yong-Moon Lee, Mi-Ock Lee, 2019, The Journal of clinical investigation.

Total synthesis of 8-oxypseudopalmatine and 8-oxypseudoberberine via ring-closing metathesis

Yong‐Chul Kim, W. Cho, D. B. Khadka, 2009 .

A Convenient Synthesis of 5‐Methylbenzo[c]phenanthridin‐6(5H)‐one.

W. Cho, I. Kim, Sun-Ja Park, 2001 .

CWJ-081, a novel 3-arylisoquinoline derivative, induces apoptosis in human leukemia HL-60 cells partially involves reactive oxygen species through c-Jun NH2-terminal kinase pathway.

Kyung-Sook Chung, Jung-Hye Choi, Kyung-Tae Lee, 2010, Bioorganic & medicinal chemistry letters.

SAR study of bisamides as cyclophilin a inhibitors for the development of host-targeting therapy for hepatitis C virus infection.

Xiaoli Li, W. Cho, Hye-won Lee, 2020, Bioorganic & medicinal chemistry.

Piperidylmethyloxychalcone improves immune-mediated acute liver failure via inhibiting TAK1 activity

J. Hong, B. Hwang, S. Han, 2017, Experimental & Molecular Medicine.

Discovery of diarylacrylonitriles as a novel series of small molecule sortase A inhibitors.

Sanghee Kim, K. Oh, W. Cho, 2004, Journal of medicinal chemistry.

Synthesis and evaluation of hydroquinone derivatives as inhibitors of Isocitrate Lyase

Sanghee Kim, K. Oh, Jongheon Shin, 2007, Archives of pharmacal research.

Repurposing of cyclophilin A inhibitors as broad-spectrum antiviral agents

Myoung Kyu Lee, W. Cho, Y. Jang, 2022, Drug Discovery Today.

Indeno[1,2-c]isoquinolines as enhancing agents on all-trans retinoic acid-mediated differentiation of human myeloid leukemia cells.

D. Cho, T. S. Kim, J. Song, 2008, Bioorganic & medicinal chemistry.

Synthesis of oxychelerythrine using lithiated toluamide-benzonitrile cycloaddition.

W. Cho, T. Le, 2005, Chemical & pharmaceutical bulletin.

Stem Cell Factor-Inducible MITF-M Expression in Therapeutics for Acquired Skin Hyperpigmentation

Song-Hee Kim, Jiyeon Lee, S. Han, 2020, Theranostics.

Discovery and Structure-Activity Relationships of Novel Template, Truncated 1'-Homologated Adenosine Derivatives as Pure Dual PPARγ/δ Modulators.

Ji Won Kim, K. Jacobson, K. Kang, 2020, Journal of medicinal chemistry.

Structure-Based Discovery of Novel Cyclophilin A Inhibitors for the Treatment of Hepatitis C Virus Infections.

T. Choi, I. Kang, J. Ha, 2015, Journal of medicinal chemistry.

Structure-based discovery and development of novel O-GlcNAcase inhibitors for the treatment of Alzheimer's disease.

Xiaoli Li, Jie He, W. Cho, 2022, European journal of medicinal chemistry.

Hydroquinone, a major component in cigarette smoke, reduces IFN-γ production in antigen-primed lymphocytes

T. S. Kim, W. Cho, B. Kang, 2008, Archives of pharmacal research.

Design and Evaluation of ω-Hydroxy Fatty Acids Containing α-GalCer Analogues for CD1d-Mediated NKT Cell Activation.

Chaemin Lim, D. Chung, W. Cho, 2014, ACS medicinal chemistry letters.

Rational design and evaluation of a branched-chain-containing glycolipid antigen that binds to CD1d.

Sanghee Kim, Chaemin Lim, W. Cho, 2010, Chemistry, an Asian journal.

The 3-Deoxy Analogue of α-GalCer: Disclosing the Role of the 4-Hydroxyl Group for CD1d-Mediated NKT Cell Activation.

Sanghee Kim, Chaemin Lim, D. Chung, 2011, ACS medicinal chemistry letters.

Identification of daidzein as a ligand of retinoic acid receptor that suppresses expression of matrix metalloproteinase-9 in HaCaT cells

Young-Gyu Kang, Mi-Ock Lee, W. Cho, 2013, Molecular and Cellular Endocrinology.

Design, synthesis, and biological evaluation of 1,3-diarylisoquinolines as novel topoisomerase I catalytic inhibitors.

W. Cho, Youngjoo Kwon, D. B. Khadka, 2018, European journal of medicinal chemistry.

Substituted 2-arylquinazolinones: Design, synthesis, and evaluation of cytotoxicity and inhibition of topoisomerases.

W. Cho, Youngjoo Kwon, H. T. Cao, 2015, European journal of medicinal chemistry.

Dihydroxylated 2,4,6-triphenyl pyridines: synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study.

P. Park, W. Cho, Youngjoo Kwon, 2012, European journal of medicinal chemistry.

2,6-Dithienyl-4-furyl pyridines: Synthesis, topoisomerase I and II inhibition, cytotoxicity, structure-activity relationship, and docking study.

Y. Na, W. Cho, Youngjoo Kwon, 2010, Bioorganic & medicinal chemistry letters.

6,7-Dimethoxy-3-(3-methoxyphenyl)isoquinolin-1-amine induces mitotic arrest and apoptotic cell death through the activation of spindle assembly checkpoint in human cervical cancer cells.

Jung-Hye Choi, Kyung-Tae Lee, Hye-Eun Choi, 2013, Carcinogenesis.

Design, synthesis, and bioactivity evaluation of novel 1-(4-(benzylsulfonyl)-2-nitrophenyl) derivatives as potential anti-inflammatory agents against LPS-induced acute lung injury.

N. Chattipakorn, G. Liang, Xiaoyu Sun, 2022, Bioorganic & medicinal chemistry letters.

Synthesis, topoisomerase I inhibition and antitumor cytotoxicity of 2,2':6',2"-, 2,2':6',3"- and 2,2':6',4"-terpyridine derivatives.

T. Jeong, S. H. Ahn, W. Cho, 2001, Bioorganic & medicinal chemistry letters.

First total synthesis of the phenolic 7,8-dihydro-8-oxoprotoberberine alkaloid, cerasonine.

W. Cho, T. Le, 2008, Chemical and pharmaceutical bulletin.

Structure-based Virtual Screening and Identification of a Novel Androgen Receptor Antagonist*

Suk Hee Cho, Keesook Lee, W. Cho, 2012, The Journal of Biological Chemistry.

Synthesis, topoisomerase I inhibition and structure-activity relationship study of 2,4,6-trisubstituted pyridine derivatives.

T. Jeong, Sun-Young Lee, Sang-Un Choi, 2004, Bioorganic & medicinal chemistry letters.

Development of 3-aryl-1-isoquinolinamines as potent antitumor agents based on CoMFA.

Kyung-Tae Lee, W. Cho, C. Ahn, 2010, European journal of medicinal chemistry.

Synthesis, in vitro and in vivo evaluation of 3-arylisoquinolinamines as potent antitumor agents.

Kyung-Tae Lee, Sang Kook Lee, Hwa-Jin Chung, 2010, Bioorganic & medicinal chemistry letters.

Synthesis of benzo[3,4]azepino[1,2-b]isoquinolin-9-ones from 3-arylisoquinolines via ring closing metathesis and evaluation of topoisomerase I inhibitory activity, cytotoxicity and docking study.

Kyung-Tae Lee, Yong‐Chul Kim, Ik-Soo Lee, 2011, Bioorganic & medicinal chemistry.

Application of ring-closing metathesis for the synthesis of benzo[3,4]azepino[1,2-b]isoquinolin-9-ones.

W. Cho, D. B. Khadka, S. Yang, 2011, Chemical & pharmaceutical bulletin.

Synthesis of 2,4-diaryl chromenopyridines and evaluation of their topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship.

Y. Na, W. Cho, Youngjoo Kwon, 2011, European journal of medicinal chemistry.

3-Arylisoquinolines as novel topoisomerase I inhibitors.

W. Cho, D. B. Khadka, 2011, Bioorganic & medicinal chemistry.

Structural modification of 3-arylisoquinolines to isoindolo[2,1-b]isoquinolinones for the development of novel topoisomerase 1 inhibitors with molecular docking study.

W. Cho, Hue Thi My Van, 2009, Bioorganic & medicinal chemistry letters.

Molecular modeling of 3-arylisoquinoline antitumor agents active against A-549. A comparative molecular field analysis study.

I. Park, W. Cho, Eung-Seok Lee, 2002, Bioorganic & medicinal chemistry.

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

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

Synthesis and biological evaluation of 3-arylisoquinolines as antitumor agents.

W. Cho, C. O. Lee, B. Chung, 1998, Bioorganic & medicinal chemistry letters.

A versatile total synthesis of benzo[c]phenanthridine and protoberberine alkaloids using lithiated toluamide-benzonitrile cycloaddition.

W. Cho, T. Le, Seong Gyoung Gang, 2004, The Journal of organic chemistry.

Synthesis of 12-oxobenzo[c]phenanthridinones and 4-substituted 3-arylisoquinolones via Vilsmeier–Haack reaction

W. Cho, Chao Zhao, D. B. Khadka, 2012 .

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

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

Virtual screening and synthesis of quinazolines as novel JAK2 inhibitors.

Kyung-Tae Lee, Suk Hee Cho, Kyung-Tae Lee, 2011, Bioorganic & medicinal chemistry.

Design, docking, and synthesis of novel indeno[1,2-c]isoquinolines for the development of antitumor agents as topoisomerase I inhibitors.

Sang Kook Lee, W. Cho, Youngjoo Kwon, 2007, Bioorganic & medicinal chemistry letters.

Synthesis of new 3-arylisoquinolinamines: effect on topoisomerase I inhibition and cytotoxicity.

S. Min, W. Cho, T. Le, 2003, Bioorganic & medicinal chemistry letters.

Design and stereoselective synthesis of conformationally constrained analogues of Zimeldine

W. Cho, G. L. Grunewald, 1996 .

Synthesis of 2-(thienyl-2-yl or -3-yl)-4-furyl-6-aryl pyridine derivatives and evaluation of their topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship.

Y. Na, W. Cho, Youngjoo Kwon, 2010, Bioorganic & medicinal chemistry.

Synthesis and Biological Evaluation of 2-Aryl-4-Aminoquinazolines as Antitumor Agents

Le Nguyen Thanh, C. Minh, V. Hue, 2015 .

Optically active tricarbonyl(η6-o-trimethylsilylbenzaldehyde)chromium(O) complexes in organic synthesis: a highly diastereoselective 1,3-dipolar cycloaddition with electron-rich olefins

W. Cho, C. Mukai, M. Hanaoka, 1993 .

Asymmetric aldol reaction : a highly Erythro-selective aldol reaction between tricarbonyl(O-trimethylsilylbenzaldehyde derivative)- chromium(0) complexes and cyclic silyl enol ethers

W. Cho, C. Mukai, M. Hanaoka, 1991 .

A highly erythro selective aldol reaction between chromium-complexed benzaldehyde derivatives and cyclic silyl enol ethers

W. Cho, C. Mukai, M. Hanaoka, 1989 .

Asymmetric Aldol Reaction: A Highly erythro‐Selective Aldol Reaction Between Tricarbonyl(o‐trimethylsilylbenzaldehyde derivative)chromium(0) Complexes and Cyclic Silyl Enol Ethers.

W. Cho, C. Mukai, M. Hanaoka, 1991 .

Design, synthesis, and antitumor evaluation of 2,4,6-triaryl pyridines containing chlorophenyl and phenolic moiety.

Y. Na, W. Cho, Youngjoo Kwon, 2012, European journal of medicinal chemistry.

Application of coupling reaction between lithiated toluamide and benzonitrile for the synthesis of phenolic benzo[c]phenanthridine alkaloid, oxyterihanine

W. Cho, Kwang Youl Lee, B. Kang, 2008, Archives of pharmacal research.

A facile synthesis of benzo[c]phenanthridine alkaloids: oxynitidine and oxysanguinarine using lithiated toluamide–benzonitrile cycloaddition

W. Cho, T. Le, Seong Gyoung Gang, 2004 .

Synthesis and Evaluation of 1,2,3-Triazole Containing Analogues of the Immunostimulant α-GalCer

Sanghee Kim, S. Ko, Hyun-Jun Youn, 2007 .

Computer-aided discovery of aminopyridines as novel JAK2 inhibitors.

Kyung-Tae Lee, W. Cho, Chao Zhao, 2015, Bioorganic & medicinal chemistry.

Synthesis and evaluation of Ketorolac ester prodrugs for transdermal delivery.

Dae-Duk Kim, Han‐Gon Choi, C. Yong, 2003, Journal of pharmaceutical sciences.

cAMP‐dependent activation of protein kinase A as a therapeutic target of skin hyperpigmentation by diphenylmethylene hydrazinecarbothioamide

J. Hong, B. Hwang, S. Han, 2015, British journal of pharmacology.

Hydroquinone regulates hemeoxygenase-1 expression via modulation of Src kinase activity through thiolation of cysteine residues.

J. Kim, B. Yoo, J. Cho, 2013, Free radical biology & medicine.

Ketorolac amide prodrugs for transdermal delivery: stability and in vitro rat skin permeation studies.

Dae-Duk Kim, Han‐Gon Choi, C. Yong, 2005, International journal of pharmaceutics.

Scoparone Exerts Anti-Tumor Activity against DU145 Prostate Cancer Cells via Inhibition of STAT3 Activity

Robert A. Harris, In-kyu Lee, K. Park, 2013, PloS one.

Structural requirement of phenylthiourea analogs for their inhibitory activity of melanogenesis and tyrosinase.

Sang-Hun Jung, Youngsoo Kim, V. Sharma, 2011, Bioorganic & medicinal chemistry letters.

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

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

Chemical transformation of protoberberines. XVII, Biomimetic introduction of an oxy functionality at the C-10 position in the benzo[c]phenanthridine skeleton : synthesis of 2,3,7,8,10-pentaoxygenated benzo[c]phenanthridine alkaloids, chelilutine and sanguilutine

W. Cho, C. Mukai, M. Hanaoka, 1991 .

A FIRST TOTAL SYNTHESIS OF ()-AMBININE

W. Cho, C. Mukai, M. Hanaoka, 1991 .

Chemical Transformation of Protoberberines. XVI. Regioselective Introduction of an Oxy Functionality at the C12-Position of the Benzo[c]phenanthridine Skeleton : A Convenient Synthesis of Macarpine from Oxychelirubine

W. Cho, C. Mukai, M. Hanaoka, 1990 .

A novel and biomimetic synthesis of chelilutine and sanguilutine.

W. Cho, C. Mukai, M. Hanaoka, 1989 .

A new and convenient synthesis of macarpine and dihydromacarpine from oxychelirubine

W. Cho, C. Mukai, M. Hanaoka, 1989 .

Chemical Transformation of Protoberberines. XI. A Novel Synthesis of 2, 3, 10, 11-Tetraoxygenated Protoberberine Alkaloids from Corresponding 2, 3, 9, 10-Tetraoxygenated Protoberberine Alkaloids

M. Marutani, W. Cho, C. Mukai, 1987 .

Convenient synthesis of indeno[1,2-c]isoquinolines as constrained forms of 3-arylisoquinolines and docking study of a topoisomerase I inhibitor into DNA-topoisomerase I complex.

T. S. Kim, W. Cho, Kwang Youl Lee, 2007, Bioorganic & medicinal chemistry letters.

Topoisomerase inhibitors as anticancer agents: a patent update

W. Cho, D. B. Khadka, 2013, Expert opinion on therapeutic patents.

Modification of 3-arylisoquinolines into 3,4-diarylisoquinolines and assessment of their cytotoxicity and topoisomerase inhibition.

W. Cho, Chao Zhao, D. B. Khadka, 2015, European journal of medicinal chemistry.

Design, synthesis and systematic evaluation of cytotoxic 3-heteroarylisoquinolinamines as topoisomerases inhibitors.

W. Cho, H. Jeong, Eung-Seok Lee, 2014, European journal of medicinal chemistry.

Pharmacological effects of berberine and its derivatives: a patent update

W. Cho, D. B. Khadka, Yifeng Jin, 2016, Expert opinion on therapeutic patents.

The discovery of 2,5-isomers of triazole-pyrrolopyrimidine as selective Janus kinase 2 (JAK2) inhibitors versus JAK1 and JAK3.

Jiwon Kim, Sun Choi, K. Kang, 2016, Bioorganic & medicinal chemistry.

Prediction of the Binding Mode of Imidacloprid and Related Compounds to House-Fly Head Acetylcholine Receptors Using Three-Dimensional QSAR Analysis

M. Akamatsu, A. Okazawa, Y. Nakagawa, 1998 .

Design and synthesis of 4-amino-2-phenylquinazolines as novel topoisomerase I inhibitors with molecular modeling.

Kyung-Tae Lee, W. Cho, Eung-Seok Lee, 2011, Bioorganic & medicinal chemistry.

Design, synthesis and docking study of 5-amino substituted indeno[1,2-c]isoquinolines as novel topoisomerase I inhibitors.

Kyung-Tae Lee, W. Cho, Eung-Seok Lee, 2011, Bioorganic & medicinal chemistry.

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.

Berberine bioisostere Q8 compound stimulates osteoblast differentiation and function in vitro

Sung Ho Lee, W. Cho, Kwang Youl Lee, 2017, Pharmacological research.

Orphan Nuclear Receptor Estrogen-Related Receptor γ (ERRγ) Is Key Regulator of Hepatic Gluconeogenesis*

S. Koo, D. Ryu, Chul-Ho Lee, 2012, The Journal of Biological Chemistry.

Comparative molecular field analysis study of stilbene derivatives active against A549 lung carcinoma.

Sanghee Kim, S. Min, W. Cho, 2003, Chemical & pharmaceutical bulletin.

Total synthesis of oxyfagaronine, phenolic benzo[c]phenanthridine and general synthetic way of 2,3,7,8- and 2,3,8,9-tetrasubstituted benzo[c]phenanthridine alkaloids.

W. Cho, T. Le, 2006, Chemical & pharmaceutical bulletin.

N-methylthioureas as new agonists of retinoic acid receptor-related orphan receptor

Mi-Ock Lee, Yohan Park, W. Cho, 2012, Archives of pharmacal research.

N-methylthioureas as new agonists of retinoic acid receptor-related orphan receptor

Yohan Park, W. Cho, Myungmo Lee, 2012, Archives of pharmacal research.

Synthesis of novel 5-oxaprotoberberines as bioisosteres of protoberberines

W. Cho, Chao Zhao, D. B. Khadka, 2014 .

Molecular design, synthesis and docking study of benz[b]oxepines and 12-oxobenzo[c]phenanthridinones as topoisomerase 1 inhibitors.

Kyung-Tae Lee, W. Cho, S. Yang, 2009, Bioorganic & medicinal chemistry letters.

First Total Synthesis of the Phenolic 7,8‐Dihydro‐8‐oxoprotoberberine Alkaloid, Cerasonine (IV)

W. Cho, T. Le, 2008 .

A Concise Synthesis of 8-Oxoberberine and Oxychelerythrine, Natural Isoquinoline Alkaloids through Biomimetic Synthetic Way

W. Cho, T. Le, 2006 .

Caffeic Acid Cyclohexylamide Rescues Lethal Inflammation in Septic Mice through Inhibition of IκB Kinase in Innate Immune Process

J. Hong, S. Han, Youngsoo Kim, 2017, Scientific Reports.

2,4-Diaryl-5,6-dihydro-1,10-phenanthroline and 2,4-diaryl-5,6-dihydrothieno[2,3-h] quinoline derivatives for topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study.

P. Park, Y. Na, W. Cho, 2012, Bioorganic chemistry.

Metformin Inhibits Hepatic Gluconeogenesis Through AMP-Activated Protein Kinase–Dependent Regulation of the Orphan Nuclear Receptor SHP

In-kyu Lee, J. Ha, Yong-soo Lee, 2008, Diabetes.

Synthetic Approaches to Natural Antioxidant Benzastatin E, F and G Analogues

W. Cho, Chao Zhao, D. B. Khadka, 2011 .

Discovery of Isoquinolinoquinazolinones as a Novel Class of Potent PPARγ Antagonists with Anti-adipogenic Effects

W. Cho, Chao Zhao, D. B. Khadka, 2016, Scientific Reports.

Structure-based discovery of pyrazolamides as novel ERRγ inverse agonists.

Hueng-Sik Choi, Don-Kyu Kim, M. Shin, 2023, European journal of medicinal chemistry.

Retinoic acid receptor–related orphan receptor α–induced activation of adenosine monophosphate–activated protein kinase results in attenuation of hepatic steatosis

Young-sil Yoon, Hyun-Jin Kang, S. Koo, 2012, Hepatology.

Novel O-benzylcinnamic acid derivative L26 treats acute lung injury in mice by MD-2.

N. Chattipakorn, Lina Yin, W. Cho, 2023, European journal of medicinal chemistry.

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.

Antiviral Activity of Isoquinolone Derivatives against Influenza Viruses and Their Cytotoxicity

Xiaoli Li, W. Cho, Y. Jang, 2021, Pharmaceuticals.

Discovery of 4-oxo-N-phenyl-1,4-dihydroquinoline-3-carboxamide derivatives as novel anti-inflammatory agents for the treatment of acute lung injury and sepsis.

N. Chattipakorn, Gaozhi Chen, Yi Wang, 2023, European journal of medicinal chemistry.

Synthesis and SAR study of novel diimide skeleton compounds with the anti-inflammatory activities in vitro and in vivo.

Xia Li, N. Chattipakorn, Wenqi Wu, 2023, Bioorganic & medicinal chemistry.

Synthesis of antineoplaston A10 analogs as potential antitumor agents

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

Pharmacokinetics of a new antitumor 3-arylisoquinoline derivative, CWJ-a-5.

C. Yong, W. Cho, S. J. Chang, 2001, International journal of pharmaceutics.

Physicochemical Properties of CWJ-a-5, a New Antitumor 3-Arylisoquinoline Derivative

B. Kang, Chi-Ho Lee, W. Cho, 2002, Drug development and industrial pharmacy.

A novel synthesis of benzo[c]phenanthridine skeleton and biological evaluation of isoquinoline derivatives.

T. Imanishi, W. Cho, B. Chung, 1999, Chemical & pharmaceutical bulletin.

Synthesis and antitumor activity of 3-arylisoquinoline derivatives

W. Cho, B. Chung, S. Yoo, 1997, Archives of pharmacal research.

6-(3,4-Dihydro-1H-isoquinoline-2-yl)-N-(6-methoxypyridine-2-yl) nicotinamide-26 (DIMN-26) decreases cell proliferation by induction of apoptosis and downregulation of androgen receptor signaling in human prostate cancer cells.

Kyung-Tae Lee, Ji-Sun Shin, W. Cho, 2016, Chemico-biological interactions.

Receptor-based discovery of a novel AR antagonist 1 Structure-Based Virtual Screening and Identification of a Novel AR Antagonist *

Keesook Lee, W. Cho, Eunsook Park, 2012 .

Design and synthesis optimization of novel diimide indoles derivatives for ameliorating acute lung injury through modulation of NF-κB signaling pathway.

N. Chattipakorn, Zhiwei Zheng, Xiaojian Shi, 2023, Bioorganic chemistry.

Design, Synthesis, and Bioevaluation of Novel MyD88 Inhibitor c17 against Acute Lung Injury Derived from the Virtual Screen.

Xia Li, Gaozhi Chen, Lina Yin, 2023, Journal of medicinal chemistry.

Novel Synthesis of the Natural Protoberberine Alkaloids: Oxypalmatine and Oxypseudopalmatine

W. Cho, T. Le, 2007 .

Novel Synthesis of the Natural Protoberberine Alkaloids: Oxypalmatine and Oxypseudopalmatine.

W. Cho, T. Le, 2007 .

Design, synthesis, and bioactivity evaluation of novel amide/sulfonamide derivatives as potential anti-inflammatory agents against acute lung injury and ulcerative colitis.

M. Guo, N. Chattipakorn, W. Cho, 2023, European journal of medicinal chemistry.

The discovery of 2,5-isomers of triazole-pyrrolopyrimidine as selective Janus kinase 2 (JAK2) inhibitors versus JAK1 and JAK3.

Jiwon Kim, Sun Choi, K. Kang, 2016, Bioorganic & medicinal chemistry.

Molecular design, synthesis and docking study of benz[b]oxepines and 12-oxobenzo[c]phenanthridinones as topoisomerase 1 inhibitors.

Kyung-Tae Lee, W. Cho, S. Yang, 2009, Bioorganic & medicinal chemistry letters.

Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study of hydroxylated 2,4-diphenyl-6-aryl pyridines.

T. Jeong, Y. Na, W. Cho, 2010, Bioorganic & medicinal chemistry.