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• Computer-aided discovery of novel AMPK activators through virtual screening and SAR-driven synthesis EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2025, v.287, 117318
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• New Insights into AMPK, as a Potential Therapeutic Target in Metabolic Dysfunction-Associated Steatotic Liver Disease and Hepatic Fibrosis BIOMOLECULES & THERAPEUTICS, 2025, v.33 no.1, 18-38
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• A novel A2a adenosine receptor inhibitor effectively mitigates hepatic fibrosis in a metabolic dysfunction-associated steatohepatitis mouse model International Journal of Biological Sciences, 2024, v.20 no.5, 1855-1870
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• Antioxidative Hyaluronic Acid-Bilirubin Nanomedicine Targeting Activated Hepatic Stellate Cells for Anti-Hepatic-Fibrosis Therapy ACS Nano, 2024, v.18 no.6, 4704-4716
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• Radiosensitizing effect of a novel CTSS inhibitor by enhancing BRCA1 protein stability in triple-negative breast cancer cells Cancer Science, 2024, v.115 no.6, 2036-2048
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• Synthesis and biological assessment of chalcone and pyrazoline derivatives as novel inhibitor for ELF3-MED23 interaction eLife, 2024, v.13
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• Cannabidiol, a Regulator of Intracellular Calcium and Calpain Cannabis and Cannabinoid Research, 2023, v.8 no.1, 119-125
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• Cervi Parvum Cornu complex for men with lower urinary tract symptoms: a multicenter, randomized, double-blind, placebo-controlled trial Prostate International, 2023, v.11 no.4, 222-227
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• Design, synthesis, and biological evaluation of novel HSP27 inhibitors to sensitize lung cancer cells to clinically available anticancer agents Bioorganic Chemistry, 2023, v.130, 106260
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• Di-indenopyridines as topoisomerase II-selective anticancer agents: Design, synthesis, and structure–activity relationships Bioorganic and Medicinal Chemistry, 2023, v.91, 117403
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• Interrupting specific hydrogen bonds between ELF3 and MED23 as an alternative drug resistance-free strategy for HER2-overexpressing cancers Journal of Advanced Research, 2023, v.47, 173-187
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• Original Article BR101801 enhances the radiosensitivity of p53-deficient colorectal cancer cells by inducing G2/M arrest, apoptosis, and senescence in a p53-independent manner AMERICAN JOURNAL OF CANCER RESEARCH, 2023, v.13 no.12, 0
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• Synthesis and evaluation of 7-(3-aminopropyloxy)-substituted flavone analogue as a topoisomerase IIα catalytic inhibitor and its sensitizing effect to enzalutamide in castration-resistant prostate cancer cells European journal of medicinal chemistry, 2023, v.246, 114999
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• Activation of the HSP27-AKT axis contributes to gefitinib resistance in non-small cell lung cancer cells independent of EGFR mutations Cellular Oncology, 2022, v.45 no.5, 913-930
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• An In-Silico Identification of Potential Flavonoids against Kidney Fibrosis Targeting TGF beta R-1 LIFE-BASEL, 2022, v.12 no.11, 1764
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• Design, Synthesis, and Cytotoxicity and Topoisomerase I/IIα Inhibition Activity of Pyrazolo[4,3-f]quinoline Derivatives Pharmaceuticals, 2022, v.15 no.4, 399
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• Discovery of (E)-3-(3-((2-Cyano-4' -dimethylaminobiphenyl-4-ylmethyl)cyclohexanecarbonylamino)-5-fluorophenyl)acrylic Acid Methyl Ester, an Intestine-Specific, FXR Partial Agonist for the Treatment of Nonalcoholic Steatohepatitis JOURNAL OF MEDICINAL CHEMISTRY, 2022, v.65 no.14, 9974-10000
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• Epigenetic regulator Cfp1 safeguards male meiotic progression by regulating meiotic gene expression EXPERIMENTAL AND MOLECULAR MEDICINE, 2022, v.54 no.8, 1098-1108
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• Epigenetic regulator Cfp1 safeguards male meiotic progression by regulating meiotic gene expression Experimental and Molecular Medicine, 2022, v.54, 1-11
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• Hypoxia-induced ELF3 promotes tumor angiogenesis through IGF1/IGF1R EMBO Reports, 2022, v.23 no.8, e52977
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• 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 European Journal of Medicinal Chemistry, 2022, v.227, 113916
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• The Risk of Gastrointestinal Cancer on Daily Intake of Low-Dose BaP in C57BL/6 for 60 Days Journal of Korean Medical Science, 2022, v.37 no.30, 1-12
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• The Risk of Gastrointestinal Cancer on Daily Intake of Low-Dose BaP in C57BL/6 for 60 Days JOURNAL OF KOREAN MEDICAL SCIENCE, 2022, v.37 no.30, e235
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• Topoisomerase IIα inhibitory and antiproliferative activity of dihydroxylated 2,6-diphenyl-4-fluorophenylpyridines: Design, synthesis, and structure-activity relationships Bioorganic and Medicinal Chemistry Letters, 2022, v.60, 128606
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• Topologically-Interlocked Minicircles as Probes of DNA Topology and DNA-Protein Interactions Chemistry - A European Journal, 2022, v.28 no.22, e202200108
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• 4-Flourophenyl-substituted 5H-indeno[1,2-b]pyridinols with enhanced topoisomerase II alpha inhibitory activity: Synthesis, biological evaluation, and structure-activity relationships BIOORGANIC CHEMISTRY, 2021, v.116, 105349
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• Ak-i-190, a new catalytic inhibitor of topoisomerase ii with anti-proliferative and pro-apoptotic activity on androgen-negative prostate cancer cells International Journal of Molecular Sciences, 2021, v.22 no.20, 11246
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• An Insight into Pathophysiological Features and Therapeutic Advances on Ependymoma CANCERS, 2021, v.13 no.13, 3221
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• Anticancer Activity of Indeno[1,2-b]-Pyridinol Derivative as a New DNA Minor Groove Binding Catalytic Inhibitor of Topoisomerase II alpha BIOMOLECULES & THERAPEUTICS, 2021, v.29 no.5, 562-570
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• COVID-19 and pulmonary fibrosis: therapeutics in clinical trials, repurposing, and potential development Archives of Pharmacal Research, 2021, v.44 no.5, 499-513
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• Discovery of a 2,4-diphenyl-5,6-dihydrobenzo(h)quinolin-8-amine derivative as a novel DNA intercalating topoisomerase IIα poison European Journal of Medicinal Chemistry, 2021, v.226, 113860
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• Drug-like small molecule HSP27 functional inhibitor sensitizes lung cancer cells to gefitinib or cisplatin by inducing altered cross-linked Hsp27 dimers Pharmaceutics, 2021, v.13 no.5, 630
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• Identification of Indicators for Preterm Birth Using Retinoid Metabolites METABOLITES, 2021, v.11 no.7, 443
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• Synthesis and structure-activity relationships of hydroxylated and halogenated 2,4-diaryl benzofuro[3,2-b]pyridin-7-ols as selective topoisomerase IIα inhibitors Bioorganic Chemistry, 2021, v.111, 104884
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• Bacterial Nucleoside Catabolism Controls Quorum Sensing and Commensal-to-Pathogen Transition in the Drosophila Gut CELL HOST & MICROBE, 2020, v.27 no.3, 345-
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• Field-based rational design of p300 histone acetyltransferase inhibitor and systematic evaluation as an anti-fibrotic agent CHEMICAL COMMUNICATIONS, 2020, v.56 no.68, 9795-9798
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• Plumbagin Suppresses Pulmonary Fibrosis Via Inhibition of p300 Histone Acetyltransferase Activity JOURNAL OF MEDICINAL FOOD, 2020, v.23 no.6, 633-640
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• Specific Roles of HSP27 S15 Phosphorylation Augmenting the Nuclear Function of HER2 to Promote Trastuzumab Resistance CANCERS, 2020, v.12 no.6, 1540
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• Synthesis, Biological Evaluation and Molecular Docking Study of Cyclic Diarylheptanoids as Potential Anticancer Therapeutics ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2020, v.20 no.4, 464-475
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• A chromenone analog as an ATP-competitive, DNA non-intercalative topoisomerase II catalytic inhibitor with preferences toward the alpha isoform CHEMICAL COMMUNICATIONS, 2019, v.55 no.85, 12857-12860
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• Discovery and Biological Evaluations of Halogenated 2,4-Diphenyl Indeno[1,2-b]pyridinol Derivatives as Potent Topoisomerase II alpha-Targeted Chemotherapeutic Agents for Breast Cancer JOURNAL OF MEDICINAL CHEMISTRY, 2019, v.62 no.17, 8194-8234
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• Recent therapeutic trends and promising targets in triple negative breast cancer Pharmacology and Therapeutics, 2019, v.199, 30-57
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• The synthesis and anticancer activities of chiral epoxy-substituted chromone analogs Bioorganic Chemistry, 2019, v.84, 347-354
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• A new phenolic series of indenopyridinone as topoisomerase inhibitors: Design, synthesis, and structure-activity relationships BIOORGANIC & MEDICINAL CHEMISTRY, 2018, v.26 no.18, 5212-5223
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• Causes of hyperhomocysteinemia and its pathological significance ARCHIVES OF PHARMACAL RESEARCH, 2018, v.41 no.4, 372-383
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• Design, synthesis, and biological evaluation of 1,3-diarylisoquinolines as novel topoisomerase I catalytic inhibitors European Journal of Medicinal Chemistry, 2018, v.143, 200-215
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• Design, synthesis, and structure-activity relationships of new benzofuro[3,2-b]pyridin-7-ols as DNA topoisomerase II inhibitors Bioorganic and Medicinal Chemistry Letters, 2018, v.28 no.4, 566-571
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• Design, synthesis, biological evaluation, structure-activity relationship study, and mode of action of 2-phenol-4,6-dichlorophenyl-pyridines BIOORGANIC CHEMISTRY, 2018, v.79, 1-18
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• Development of 13H-benzo[f]chromeno[4,3-b][1,7]naphthyridines and their salts as potent cytotoxic agents and topoisomerase I/II alpha inhibitors BIOORGANIC & MEDICINAL CHEMISTRY, 2018, v.26 no.18, 5181-5193
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• Hyperactivated m-calpain affects acquisition of doxorubicin resistance in breast cancer cells Biochimica et Biophysica Acta - General Subjects, 2018, v.1862 no.5, 1126-1133
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• Intestinal P-glycoprotein inhibitors, benzoxanthone analogues JOURNAL OF PHARMACY AND PHARMACOLOGY, 2018, v.70 no.2, 234-241
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• Linear diarylheptanoids as potential anticancer therapeutics: synthesis, biological evaluation, and structure-activity relationship studies ARCHIVES OF PHARMACAL RESEARCH, 2018, v.41 no.12, 1131-1148
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• Modification of translationally controlled tumor protein-derived protein transduction domain for improved intranasal delivery of insulin DRUG DELIVERY, 2018, v.25 no.1, 1025-1032
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• Synthesis and SAR study of new hydroxy and chloro-substituted 2,4-diphenyl 5H-chromeno[4,3-b]pyridines as selective topoisomerase II alpha-targeting anticancer agents BIOORGANIC & MEDICINAL CHEMISTRY, 2018, v.26 no.8, 1909-1919
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• 2-Chlorophenyl-substituted benzofuro[3,2-b] pyridines with enhanced topoisomerase inhibitory activity: The role of the chlorine substituent BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2017, v.27 no.15, 3279-3283
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• A novel indeno[1,2-b] pyridinone derivative, a DNA intercalative human topoisomerase II alpha catalytic inhibitor, for caspase 3-independent anticancer activity CHEMICAL COMMUNICATIONS, 2017, v.53 no.51
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• Antiepileptic and Neuroprotective Effects of Oleamide in Rat Striatum on Kainate-Induced Behavioral Seizure and Excitotoxic Damage via Calpain Inhibition FRONTIERS IN PHARMACOLOGY, 2017, v.8, 817
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• BMI-1 interacts with sMEK1 and inactivates sMEK1-induced apoptotic cell death Oncology Reports, 2017, v.37 no.1, 579-586
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• Design, synthesis and biological evaluation of 1,3-diphenylbenzo[f] [1,7]naphthyrdines BIOORGANIC & MEDICINAL CHEMISTRY, 2017, v.25 no.20, 5586-5597
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• Dihydroxylated 2,6-diphenyl-4-chlorophenylpyridines: Topoisomerase I and II alpha dual inhibitors with DNA non-intercalative catalytic activity EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, v.133, 69-84
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• Fluorescein hydrazones: A series of novel non-intercalative topoisomerase IIα catalytic inhibitors induce G1 arrest and apoptosis in breast and colon cancer cells European Journal of Medicinal Chemistry, 2017, v.125, 49-67
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• Novel 2-aryl-4-(4′-hydroxyphenyl)-5H-indeno[1,2-b]pyridines as potent DNA non-intercalative topoisomerase catalytic inhibitors European Journal of Medicinal Chemistry, 2017, v.125, 14-28
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• 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 European Journal of Medicinal Chemistry, 2017, v.127, 318-333
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• Sensitization of lung cancer cells by altered dimerization of HSP27 Oncotarget, 2017, v.8 no.62, 105372-105382
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• Synthesis and biological effect of chrom-4-one derivatives as functional inhibitors of heat shock protein 27 EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, v.139, 892-900
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• The Conjugated Double Bond of Coniferyl Aldehyde Is Essential for Heat Shock Factor 1 Mediated Cytotoprotection Journal of Natural Products, 2017, v.80 no.8, 2379-2383
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• The synthesis of tamoxifen-loaded albumin nanoparticles by homogenizers: Optimization and in vitro characterization Journal of Drug Delivery Science and Technology, 2017, v.41, 20-30
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• 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 European Journal of Medicinal Chemistry, 2016, v.113, 228-245
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• Calcium influx-mediated translocation of m-calpain induces Ku80 cleavage and enhances the Ku80-related DNA repair pathway ONCOTARGET, 2016, v.7 no.21, 30831-30844
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• 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 Bioorganic and Medicinal Chemistry, 2016, v.24 no.8
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• Effect of chlorine substituent on cytotoxic activities: Design and synthesis of systematically modified 2,4-diphenyl-5H-indeno[1,2-b]pyridines BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2016, v.26 no.7, 1726-1731
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• MARCKSL1 exhibits anti-angiogenic effects through suppression of VEGFR-2-dependent Akt/PDK-1/mTOR phosphorylation Oncology Reports, 2016, v.35 no.2, 1041-1048
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• 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 European Journal of Medicinal Chemistry, 2016, v.121, 433-444
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• Overcoming HSP27-mediated resistance by altered dimerization of HSP27 using small molecules ONCOTARGET, 2016, v.7 no.33, 53178-53190
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• Proposal of Dual Inhibitor Targeting ATPase Domains of Topoisomerase II and. Heat Shock Protein 90 BIOMOLECULES & THERAPEUTICS, 2016, v.24 no.5, 453-468
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• Synthesis and biological evaluation of 2-phenol-4-chlorophenyl-6-aryl pyridines as topoisomerase II inhibitors and cytotoxic agents BIOORGANIC CHEMISTRY, 2016, v.66, 145-159
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• Synthesis and biological evaluation of C1-O-substituted-3-(3-butylamino-2-hydroxy-propoxy)-xanthen-9-one as topoisomerase II alpha catalytic inhibitors EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2016, v.123, 211-225
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• Synthesis and topoisomerases inhibitory activity of heteroaromatic chalcones BIOORGANIC & MEDICINAL CHEMISTRY, 2016, v.24 no.22, 5921-5928
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• A Series of Novel Terpyridine-Skeleton Molecule Derivants Inhibit Tumor Growth and Metastasis by Targeting Topoisomerases JOURNAL OF MEDICINAL CHEMISTRY, 2015, v.58 no.3, 1100-1122
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• Benzo[b]Tryptanthrin Inhibits MDR1, Topoisomerase Activity, and Reverses Adriamycin Resistance in Breast Cancer Cells ChemMedChem, 2015, v.10 no.5, 827-835
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• Design and synthesis of conformationally constrained hydroxylated 4-phenyl-2-aryl chromenopyridines as novel and selective topoisomerase II-targeted antiproliferative agents Bioorganic and Medicinal Chemistry, 2015, v.23 no.19, 6454-6466
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• Design and synthesis of novel 2,4-diaryl-5H-indeno[1,2-b]pyridine derivatives, and their evaluation of topoisomerase inhibitory activity and cytotoxicity Bioorganic and Medicinal Chemistry, 2015, v.23 no.1, 160-173
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• Modification of 3-arylisoquinolines into 3,4-diarylisoquinolines and assessment of their cytotoxicity and topoisomerase inhibition European Journal of Medicinal Chemistry, 2015, v.92, 583-607
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• Modified 2,4-diaryl-5H-indeno[1,2-b]pyridines with hydroxyl and chlorine moiety: Synthesis, anticancer activity, and structure-activity relationship study Bioorganic Chemistry, 2015, v.62, 30-40
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• Substituted 2-arylquinazolinones: Design, synthesis, and evaluation of cytotoxicity and inhibition of topoisomerases European Journal of Medicinal Chemistry, 2015, v.103, 69-79
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• Synthesis and biological activity of 2,4-di- p -phenolyl-6- 2 -furanyl-pyridine as a potent topoisomerase II poison European Journal of Medicinal Chemistry, 2015, v.90, 360-378
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• Synthesis and in vitro screening of phenylbipyridinylpyrazole derivatives as potential antiproliferative agents Molecules, 2015, v.20 no.1, 1031-1045
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• 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 Bioorganic and Medicinal Chemistry, 2015, v.23 no.13
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• Topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study of dihydroxylated 2,6-diphenyl-4-aryl pyridines Bioorganic and Medicinal Chemistry, 2015, 2015
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• Xanthone analogues as potent modulators of intestinal P-glycoprotein EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2015, v.93, 237-245
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• sMEK1 inhibits endothelial cell proliferation by attenuating VEGFR-2-dependent-Akt/eNOS/HIF-1 alpha signaling pathways ONCOTARGET, 2015, v.6 no.31, 31830-31843
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• Cobalt-albumin binding (CAB) assay: An advantageous and flaw free testing of albumin-cobalt binding Journal of Pharmaceutical and Biomedical Analysis, 2014, v.99, 79-82
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• Design, synthesis and systematic evaluation of cytotoxic 3-heteroarylisoquinolinamines as topoisomerases inhibitors European Journal of Medicinal Chemistry, 2014, v.82, 181-194
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• Development of an Albumin Copper Binding (ACuB) Assay to Detect Ischemia Modified Albumin ANALYTICAL SCIENCES, 2014, v.30 no.10, 985-990
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• Discovery of dihydroxylated 2,4-diphenyl-6-thiophen-2-yl-pyridine as a non-intercalative DNA-binding topoisomerase II-specific catalytic inhibitor EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, v.80 no., 428-438
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• 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 BIOORGANIC & MEDICINAL CHEMISTRY, 2014, v.22 no.17, 4553-4565
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• Evaluation of albumin structural modifications through cobalt-albumin binding (CAB) assay JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2014, v.91, 17-23
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• Fluorescein Hydrazones as Novel Nonintercalative Topoisomerase Catalytic Inhibitors with Low DNA Toxicity JOURNAL OF MEDICINAL CHEMISTRY, 2014, v.57 no.21, 9139-9151
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• Hydroxylated 2,4-diphenyl indenopyridine derivatives as a selective non-intercalative topoisomerase catalytic inhibitor European Journal of Medicinal Chemistry, 2014, v.90, 302-314
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• Reply to the Letter to the Editor "Cobalt-albumin binding (CAB) assay: An advantageous and flaw free testing of albumin-cobalt binding" JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2014, v.99, 81-82
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• Synthesis, antitumor,activity, and structure-activity relationship study of trihydroxylated 2,4,6-triphenyl pyridines as potent and selective topoisomerase II inhibitors EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, v.84, 555-565
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• [학술지논문] Cannabidiol, a Regulator of Intracellular Calcium and Calpain CANNABIS AND CANNABINOID RESEARCH , 2023, v.11 no.111 , 1-7
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• [학술지논문] Editorial: Small organic molecules with anticancer activity FRONTIERS IN CHEMISTRY, 2023, v.11 no.2023 , 1-2
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• [학술지논문] Original Article BR101801 enhances the radiosensitivity of p53-deficient colorectal cancer cells by inducing G2/M arrest, apoptosis, and senescence in a p53-independent manner AMERICAN JOURNAL OF CANCER RESEARCH, 2023, v.13 no.12 , 5887-5900
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• [학술지논문] Roles of Coffee and Its Components in Liver Diseases Drug Targets and Therapeutics, 2023, v.2 no.2 , 133-144
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• [학술지논문] Synthesis and evaluation of 7-(3-aminopropyloxy)-substituted flavone analogue as a topoisomerase IIα catalytic inhibitor and its sensitizing effect to enzalutamide in castration-resistant prostate cancer cells EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2023, v.246 no.114999 , 1-16
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• [학술지논문] An In-Silico Identification of Potential Flavonoids against Kidney Fibrosis Targeting TGF beta R-1 LIFE-BASEL, 2022, v.12 no.11 , 1764-1764
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• [학술지논문] Hypoxia-induced ELF3 promotes tumor angiogenesis through IGF1/IGF1R EMBO REPORTS, 2022, v.23 no.8 , 52977-52977
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