Y. Kwon

Yun‐Sil Lee, Y. Jin, Y. Na, 2013, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Dihydroxylated 2,6-diphenyl-4-chlorophenylpyridines: Topoisomerase I and IIα dual inhibitors with DNA non-intercalative catalytic activity.

G. Bist, Eung-Seok Lee, Seojeong Park, 2017, European journal of medicinal chemistry.

Synthesis and biological activity of 2,4-di-p-phenolyl-6-2-furanyl-pyridine as a potent topoisomerase II poison.

Youngjoo Kwon, Kyu-Yeon Jun, T. Kadayat, 2015, European journal of medicinal chemistry.

Thiol-reducing agents prevent sulforaphane-induced growth inhibition in ovarian cancer cells

Seung Cheol Kim, Youngjoo Kwon, Boyun Choi, 2017, Food & nutrition research.

Intestinal P‐glycoprotein inhibitors, benzoxanthone analogues

H. Lee, Y. Na, J. Park, 2018, The Journal of pharmacy and pharmacology.

Xanthone analogues as potent modulators of intestinal P-glycoprotein.

H. Lee, Y. Na, Youngjoo Kwon, 2015, European journal of medicinal chemistry.

Drug-Like Small Molecule HSP27 Functional Inhibitor Sensitizes Lung Cancer Cells to Gefitinib or Cisplatin by Inducing Altered Cross-Linked Hsp27 Dimers

H. Lee, Yun‐Sil Lee, Y. Na, 2021, Pharmaceutics.

COVID-19 and pulmonary fibrosis: therapeutics in clinical trials, repurposing, and potential development

Y. Kwon, H. Lim, J. Yim, 2021, Archives of Pharmacal Research.

PTN signaling: Components and mechanistic insights in human ovarian cancer

A. Godwin, O. Tawfik, R. Madan, 2015, Molecular carcinogenesis.

The synthesis of tamoxifen-loaded albumin nanoparticles by homogenizers: Optimization and in vitro characterization

F. Dorkoosh, Kang-Choon Lee, S. Shojaosadati, 2017 .

Effect of soy isoflavones on the growth of human breast tumors: findings from preclinical studies

Y. Kwon, 2014, Food science & nutrition.

Food-derived polyphenols inhibit the growth of ovarian cancer cells irrespective of their ability to induce antioxidant responses

Youngjoo Kwon, Y. Kwon, 2018, Heliyon.

A-62176, a potent topoisomerase inhibitor, inhibits the expression of human epidermal growth factor receptor 2.

Yongmun Choi, Y. Na, Dae-Kee Kim, 2012, Cancer letters.

Aging alters acute apoptotic response to azoxymethane in the colon of rats

B. Magnuson, Y. Kwon, 2007, Experimental Gerontology.

A facile synthesis of emodin derivatives, emodin carbaldehyde, citreorosein, and their 10-deoxygenated derivatives and their inhibitory activities on μ-calpain

H. Chang, Seung Ho Lee, Youngjoo Kwon, 2012, Archives of pharmacal research.

A facile synthesis of emodin derivatives, emodin carbaldehyde, citreorosein, and their 10-deoxygenated derivatives and their inhibitory activities on μ-calpain

H. Chang, Y. Jahng, J. Liang, 2012, Archives of Pharmacal Research.

Development of an albumin copper binding (ACuB) assay to detect ischemia modified albumin.

M. Suh, G. Jhon, Youngjoo Kwon, 2014, Analytical sciences : the international journal of the Japan Society for Analytical Chemistry.

Neuroprotective effect of undecylenic acid extracted from Ricinus communis L. through inhibition of μ-calpain.

Ji-Eun Eom, Eunyoung Lee, D. Jung, 2012, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Novel N-4-piperazinyl-ciprofloxacin-chalcone hybrids: synthesis, physicochemical properties, anticancer and topoisomerase I and II inhibitory activity.

Youngjoo Kwon, M. Sayed, G. E. Abuo-Rahma, 2013, European journal of medicinal chemistry.

Calcium influx-mediated translocation of m-calpain induces Ku80 cleavage and enhances the Ku80-related DNA repair pathway

Eosu Kim, Y. Na, Han Yu, 2016, Oncotarget.

A novel indeno[1,2-b]pyridinone derivative, a DNA intercalative human topoisomerase IIα catalytic inhibitor, for caspase 3-independent anticancer activity.

C. Park, T. Kadayat, K. Jeon, 2017, Chemical communications.

Synthesis and biological evaluation of C1-O-substituted-3-(3-butylamino-2-hydroxy-propoxy)-xanthen-9-one as topoisomerase IIα catalytic inhibitors.

Y. Na, Youngjoo Kwon, Kyu-Yeon Jun, 2016, European journal of medicinal chemistry.

A new series of 2-phenol-4-aryl-6-chlorophenyl pyridine derivatives as dual topoisomerase I/II inhibitors: Synthesis, biological evaluation and 3D-QSAR study.

Y. Na, T. Kadayat, G. Bist, 2016, European journal of medicinal chemistry.

Modified 2,4-diaryl-5H-indeno[1,2-b]pyridines with hydroxyl and chlorine moiety: Synthesis, anticancer activity, and structure-activity relationship study.

Youngjoo Kwon, T. Kadayat, Eung-Seok Lee, 2015, Bioorganic chemistry.

Identification of new halogen-containing 2,4-diphenyl indenopyridin-5-one derivative as a boosting agent for the anticancer responses of clinically available topoisomerase inhibitors.

M. Seo, Youngjoo Kwon, T. Kadayat, 2021, European journal of 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.

Hyperactivated m-calpain affects acquisition of doxorubicin resistance in breast cancer cells.

Youngjoo Kwon, Han Yu, K. Jeon, 2018, Biochimica et biophysica acta. General subjects.

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.

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.

Antiepileptic and Neuroprotective Effects of Oleamide in Rat Striatum on Kainate-Induced Behavioral Seizure and Excitotoxic Damage via Calpain Inhibition

Hwa‐Jung Kim, Youngjoo Kwon, Hyeyeon Nam, 2017, Front. Pharmacol..

Topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study of dihydroxylated 2,6-diphenyl-4-aryl pyridines.

Y. Na, Youngjoo Kwon, T. Kadayat, 2010, Bioorganic & medicinal chemistry.

Rapid and reliable measurement for evaluating directly the reactivity of N-acetylcysteine with glucose degradation products in peritoneal dialysis fluids.

H. Ha, Eun-young Seo, Eunyoung Lee, 2011, Analytical chemistry.

Protective Effect of Gastrodia Elata on Neuronal Cell Damage in Alzheimer's Disease

Byung-Soo Koo, Jae-Hyun Kang, G. Kim, 2010 .

Effect of trans–fatty acids on lipid metabolism: Mechanisms for their adverse health effects

Youngjoo Kwon, Y. Kwon, 2016 .

Effect of conjugated linoleic acid, μ-calpain inhibitor, on pathogenesis of Alzheimer's disease.

I. Mook‐Jung, Minyung Lee, Ji-Eun Eom, 2013, Biochimica et biophysica acta.

Development of a database of capsaicinoid contents in foods commonly consumed in Korea

Youngjoo Kwon, Hoyoun Cho, Y. Kwon, 2020, Food science & nutrition.

The Conjugated Double Bond of Coniferyl Aldehyde Is Essential for Heat Shock Factor 1 Mediated Cytotoprotection.

Yun‐Sil Lee, Y. Na, Youngjoo Kwon, 2017, Journal of natural products.

Topologically-Interlocked Minicircles as Probes of DNA Topology and DNA-Protein Interactions.

A. Rajendran, T. Morii, Eiji Nakata, 2022, Chemistry.

Synthesis and SAR study of new hydroxy and chloro-substituted 2,4-diphenyl 5H-chromeno[4,3-b]pyridines as selective topoisomerase IIα-targeting anticancer agents.

S. Seo, Youngjoo Kwon, T. Kadayat, 2018, Bioorganic & medicinal chemistry.

Sensitization of lung cancer cells by altered dimerization of HSP27

H. Lee, Yun‐Sil Lee, Y. Na, 2017, Oncotarget.

Synthesis and biological effect of chrom-4-one derivatives as functional inhibitors of heat shock protein 27.

Yun‐Sil Lee, Y. Na, S. Kwak, 2017, European journal of medicinal chemistry.

Design, synthesis, and biological evaluation of novel HSP27 inhibitors to sensitize lung cancer cells to clinically available anticancer agents.

Yun‐Sil Lee, Y. Na, Hawon Yoo, 2022, Bioorganic chemistry.

The synthesis and anticancer activities of chiral epoxy-substituted chromone analogs.

Y. Na, Youngjoo Kwon, Hyunji Jo, 2019, Bioorganic chemistry.

Overcoming HSP27-mediated resistance by altered dimerization of HSP27 using small molecules

Yun‐Sil Lee, Y. Na, Naery Lee, 2016, Oncotarget.

Specific Roles of HSP27 S15 Phosphorylation Augmenting the Nuclear Function of HER2 to Promote Trastuzumab Resistance

Yun‐Sil Lee, S. Seo, Y. Na, 2020, Cancers.

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.

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.

Effective Inhibition of c-MET-mediated Signaling, Growth, and Migration of Ovarian Cancer Cells is Influenced by the Ovarian Tissue Microenvironment

Yan Zhou, A. Godwin, Michael D. Kaufman, 2013, Oncogene.

Synthesis and Biological Properties of Luotonin a Derivatives

A. Rahman, Y. Na, Youngjoo Kwon, 2008 .

Design and synthesis of conformationally constrained hydroxylated 4-phenyl-2-aryl chromenopyridines as novel and selective topoisomerase II-targeted antiproliferative agents.

Y. Na, Youngjoo Kwon, Kyu-Yeon Jun, 2015, Bioorganic & medicinal chemistry.

Hydroxylated 2,4-diphenyl indenopyridine derivatives as a selective non-intercalative topoisomerase IIα catalytic inhibitor.

Youngjoo Kwon, Kyu-Yeon Jun, T. Kadayat, 2015, European journal of medicinal chemistry.

Design and synthesis of novel 2,4-diaryl-5H-indeno[1,2-b]pyridine derivatives, and their evaluation of topoisomerase inhibitory activity and cytotoxicity.

Youngjoo Kwon, Kyu-Yeon Jun, T. Kadayat, 2015, Bioorganic & medicinal chemistry.

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.

Synthesis, Topoisomerase I and II Inhibitory Activity, Cytotoxicity, and Structure-activity Relationship Study of Rigid Analogues of 2,4,6-Trisubstituted Pyridine Containing 5,6-Dihydrobenzo(h)quinoline Moiety

Y. Na, Youngjoo Kwon, Eun-Mi Ha, 2011 .

Synthesis, Topoisomerase I and II Inhibitory Activities, and Cytotoxicity of 4,6-Diaryl-2,4'-bipyridine Derivatives

Pritam Thapa, Eung-Seok Lee, Radha Karki, 2010 .

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.

2-Thienyl-4-furyl-6-aryl pyridine derivatives: synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study.

Y. Na, Youngjoo Kwon, Y. Jahng, 2010, Bioorganic & 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.

A new phenolic series of indenopyridinone as topoisomerase inhibitors: Design, synthesis, and structure-activity relationships.

Youngjoo Kwon, Eung-Seok Lee, Aarajana Shrestha, 2018, Bioorganic & medicinal chemistry.

Design, synthesis, and structure-activity relationships of new benzofuro[3,2-b]pyridin-7-ols as DNA topoisomerase II inhibitors.

Hyunji Jo, Eung-Seok Lee, Y. Kwon, 2018, Bioorganic & medicinal chemistry letters.

Design, synthesis, topoisomerase I & II inhibitory activity, antiproliferative activity, and structure-activity relationship study of pyrazoline derivatives: An ATP-competitive human topoisomerase IIα catalytic inhibitor.

A. Rahman, A. Kadi, H. Abdel‐Aziz, 2016, Bioorganic & medicinal chemistry.

New insight for fluoroquinophenoxazine derivatives as possibly new potent topoisomerase I inhibitor.

Y. Na, Youngjoo Kwon, Y. Jahng, 2008, Bioorganic & medicinal chemistry letters.

B. Magnuson, Y. Kwon, 2009, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

Discovery of a 2,4-diphenyl-5,6-dihydrobenzo(h)quinolin-8-amine derivative as a novel DNA intercalating topoisomerase IIα poison.

T. Kadayat, Eung-Seok Lee, Daeun Kim, 2021, European journal of medicinal chemistry.

2-Chlorophenyl-substituted benzofuro[3,2-b]pyridines with enhanced topoisomerase inhibitory activity: The role of the chlorine substituent.

Hwa-Jong Lee, T. Kadayat, G. Bist, 2017, Bioorganic & medicinal chemistry letters.

Chalcones, inhibitors for topoisomerase I and cathepsin B and L, as potential anti-cancer agents.

Y. Na, Seok-Ho Kim, Eung-Seok Lee, 2013, Bioorganic & medicinal chemistry letters.

Synthesis and biological properties of benzo-annulated rutaecarpines.

Seung Ho Lee, Youngjoo Kwon, Y. Jahng, 2010, Biological & pharmaceutical bulletin.

Anticancer Activity of Indeno[1,2-b]-Pyridinol Derivative as a New DNA Minor Groove Binding Catalytic Inhibitor of Topoisomerase IIα

M. Seo, Eung-Seok Lee, Jeong-Ahn Kim, 2021, Biomolecules & therapeutics.

Synthesis, Biological Evaluation and Molecular Docking Study of Cyclic Diarylheptanoids as Potential Anticancer Therapeutics.

A. Kadi, Y. Jahng, M. Alam, 2019, Anti-cancer agents in medicinal chemistry.

Small molecule transcription factor mimic.

P. Dervan, M. Uesugi, Yongmun Choi, 2004, Journal of the American Chemical Society.

A wrench-shaped synthetic molecule that modulates a transcription factor-coactivator interaction.

M. Uesugi, Yongmun Choi, Y. Kawazoe, 2004, Journal of the American Chemical Society.

Use of saw palmetto (Serenoa repens) extract for benign prostatic hyperplasia

Youngjoo Kwon, Y. Kwon, 2019, Food Science and Biotechnology.

Luteolin as a potential preventive and therapeutic candidate for Alzheimer's disease

Y. Kwon, 2017, Experimental Gerontology.

Anthocyanin-Rich Extracts Inhibit Multiple Biomarkers of Colon Cancer in Rats

B. Magnuson, M. Giusti, Jian He, 2006, Nutrition and cancer.

Estimation of curcumin intake in Korea based on the Korea National Health and Nutrition Examination Survey (2008-2012)

Youngjoo Kwon, Y. Kwon, 2014, Nutrition research and practice.

Estimation of Dietary Capsaicinoid Exposure in Korea and Assessment of Its Health Effects

Youngjoo Kwon, Y. Kwon, 2021, Nutrients.

Synthesis and structure-activity relationships of hydroxylated and halogenated 2,4-diaryl benzofuro[3,2-b]pyridin-7-ols as selective topoisomerase IIα inhibitors.

Youngjoo Kwon, G. Bist, Eung-Seok Lee, 2021, Bioorganic chemistry.

Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study of 2-phenyl- or hydroxylated 2-phenyl-4-aryl-5H-indeno[1,2-b]pyridines.

Y. Na, Youngjoo Kwon, Pritam Thapa, 2015, Bioorganic & medicinal chemistry.

Synthesis and in Vitro Screening of Phenylbipyridinylpyrazole Derivatives as Potential Antiproliferative Agents

Byung Sun Park, M. M. Al-Sanea, I. Kim, 2015, Molecules.

Discovery of dihydroxylated 2,4-diphenyl-6-thiophen-2-yl-pyridine as a non-intercalative DNA-binding topoisomerase II-specific catalytic inhibitor.

Pritam Thapa, Eung-Seok Lee, Radha Karki, 2014, European journal of medicinal chemistry.

New benzoxanthone derivatives as topoisomerase inhibitors and DNA cross-linkers.

Y. Na, Youngjoo Kwon, M. Jung, 2010, Bioorganic & medicinal chemistry.

Oxiranylmethyloxy or thiiranylmethyloxy-azaxanthones and -acridone analogues as potential topoisomerase I inhibitors.

Y. Na, Youngjoo Kwon, M. Jung, 2009, Bioorganic & medicinal chemistry letters.

Synthesis, Cytotoxicity and Topoisomerase II Inhibition Study of New Thioxanthone Analogues.

Y. Na, Youngjoo Kwon, Y. Jahng, 2008 .

Regulation of HGF and c-MET Interaction in Normal Ovary and Ovarian Cancer: Importance of Targeting c-MET and HGF Interaction.

A. Godwin, Y. Kwon, 2017 .

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.

P‐Glycoprotein Inhibitory Activity of Two Phenolic Compounds, (−)‐Syringaresinol and Tricin from Sasa borealis

D. Jang, S. Chung, Ah-Reum Han, 2007, Chemistry & biodiversity.

Synthesis and topoisomerases inhibitory activity of heteroaromatic chalcones.

Y. Na, Han Yu, S. Kwak, 2016, Bioorganic & medicinal chemistry.

Differential Expressions of Adhesive Molecules and Proteases Define Mechanisms of Ovarian Tumor Cell Matrix Penetration/Invasion

Andrew K. Godwin, A. Godwin, E. Cukierman, 2011, PloS one.

Effect of azoxymethane and curcumin on transcriptional levels of cyclooxygenase-1 and -2 during initiation of colon carcinogenesis

B. Magnuson, Y. Kwon, 2007, Scandinavian journal of gastroenterology.

Two New Diarylheptanoids from Juglans mandshurica

H. Chang, M. Woo, Y. Jahng, 2005 .

3-(3-Butylamino-2-hydroxy-propoxy)-1-hydroxy-xanthen-9-one acts as a topoisomerase IIα catalytic inhibitor with low DNA damage.

Y. Na, Eung-Seok Lee, Eunyoung Lee, 2013, European journal of medicinal chemistry.

Rapid determination of trace methylmercury in natural crude medicine of animal origin

D. Kwon, Mi‐jeong Kim, Shin-Jung Kang, 2009 .

2,2-dimethyl-2H-pyran-derived alkaloids I. Practical synthesis of acronycine and benzo[b]acronycine and their biological properties

Seung Ho Lee, Youngjoo Kwon, Y. Jahng, 2008, Archives of pharmacal research.

Synthesis and investigation of dihydroxychalcones as calpain and cathepsin inhibitors.

Y. Na, Youngjoo Kwon, Eung-Seok Lee, 2013, Bioorganic chemistry.

Evaluation of albumin structural modifications through cobalt-albumin binding (CAB) assay.

G. Jhon, Youngjoo Kwon, Ji-Eun Eom, 2014, Journal of pharmaceutical and biomedical analysis.

Effect of chlorine substituent on cytotoxic activities: Design and synthesis of systematically modified 2,4-diphenyl-5H-indeno[1,2-b]pyridines.

Y. Na, Youngjoo Kwon, Kyu-Yeon Jun, 2016, Bioorganic & medicinal chemistry letters.

A chromenone analog as an ATP-competitive, DNA non-intercalative topoisomerase II catalytic inhibitor with preferences toward the alpha isoform.

Y. Na, Hyunji Jo, Seojeong Park, 2019, Chemical communications.

Synthesis and pharmacological evaluation of new methyloxiranylmethoxyxanthone analogues.

Y. Na, Youngjoo Kwon, Eun-Mi Ha, 2010, European journal of medicinal chemistry.

Synthesis of benzo-annulated tryptanthrins and their biological properties.

Youngjoo Kwon, Y. Jahng, J. Liang, 2012, Bioorganic & medicinal chemistry.

Inhibition of Colonic Aberrant Crypt Foci by Curcumin in Rats Is Affected by Age

B. Magnuson, Youngjoo Kwon, M. Malik, 2004, Nutrition and cancer.

Mutations in SOHLH1 gene associate with nonobstructive Azoospermia

Dong Ryul Lee, A. Rajkovic, Ji-Young Kim, 2010, Human mutation.

Neuroprotective effect of synthetic chalcone derivatives as competitive dual inhibitors against μ-calpain and cathepsin B through the downregulation of tau phosphorylation and insoluble Aβ peptide formation.

Y. Na, Ji-Eun Eom, S. Kwak, 2016, European journal of medicinal chemistry.

Proposal of Dual Inhibitor Targeting ATPase Domains of Topoisomerase II and Heat Shock Protein 90

Y. Kwon, Kyu‐Yeon Jun, 2016, Biomolecules & therapeutics.

Design, synthesis, biological evaluation, structure-activity relationship study, and mode of action of 2-phenol-4,6-dichlorophenyl-pyridines.

G. Bist, Eung-Seok Lee, Seojeong Park, 2018, Bioorganic chemistry.

Synthesis, biological evaluation, and molecular docking study of 3-(3'-heteroatom substituted-2'-hydroxy-1'-propyloxy) xanthone analogues as novel topoisomerase IIα catalytic inhibitor.

Y. Na, Youngjoo Kwon, Kyu-Yeon Jun, 2011, European journal of medicinal chemistry.

Field-based rational design of p300 histone acetyltransferase inhibitor and systematic evaluation as an anti-fibrotic agent.

M. Sohn, Ho-Geun Yoon, Soo-yeon Park, 2020, Chemical communications.

Plumbagin Suppresses Pulmonary Fibrosis Via Inhibition of p300 Histone Acetyltransferase Activity.

M. Sohn, Ho-Geun Yoon, M. J. Kim, 2020, Journal of medicinal food.

Synthesis and biological evaluation of 2-phenol-4-chlorophenyl-6-aryl pyridines as topoisomerase II inhibitors and cytotoxic agents.

Y. Na, Pritam Thapa, T. Kadayat, 2016, Bioorganic chemistry.

Synthesis of new xanthone analogues and their biological activity test--cytotoxicity, topoisomerase II inhibition, and DNA cross-linking study.

Y. Na, Youngjoo Kwon, Chong-soon Lee, 2007, Bioorganic & medicinal chemistry letters.

Ethyl 2-(benzylidene)-7-methyl-3-oxo-2,3-dihydro-5H-thiazolo[3,2-a]pyrimidine-6-carboxylate analogues as a new scaffold for protein kinase casein kinase 2 inhibitor.

Kunhong Kim, Y. Na, S. Kim, 2014, Bioorganic & medicinal chemistry.

Effect of chlorine substituent on cytotoxic activities: Design and synthesis of systematically modified 2,4-diphenyl-5H-indeno[1,2-b]pyridines.

Y. Na, T. Kadayat, G. Bist, 2016, Bioorganic & medicinal chemistry letters.

Rational design, synthesis, and evaluation of novel 2,4-Chloro- and Hydroxy-Substituted diphenyl Benzofuro[3,2-b]Pyridines: Non-intercalative catalytic topoisomerase I and II dual inhibitor.

Youngjoo Kwon, Hwa-Jong Lee, T. Kadayat, 2017, European journal of medicinal chemistry.

Discovery and Biological Evaluations of Halogenated 2,4-Diphenyl Indeno[1,2-b]pyridinol Derivatives as Potent Topoisomerase IIα-targeted Chemotherapeutic Agents for Breast Cancer.

T. Jeong, Kil-Soo Kim, Youngjoo Kwon, 2019, Journal of 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.

Association of curry consumption with blood lipids and glucose levels

Youngjoo Kwon, Y. Kwon, 2016, Nutrition research and practice.

Synthesis and biological effect of chrom-4-one derivatives as functional inhibitors of heat shock protein 27.

Yun‐Sil Lee, Y. Na, S. Kwak, 2017, European journal of medicinal chemistry.

Dithiiranylmethyloxy azaxanthone shows potent anti-tumor activity via suppression of HER2 expression and HER2-mediated signals in HER2-overexpressing breast cancer cells.

Yun‐Sil Lee, Y. Jin, Y. Na, 2013, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

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.