2011 | 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 | 권영주 | Article |
2009 | Synthesis of isoquinolinone-based tetracycles as poly (ADP-ribose) polymerase-1 (PARP-1) inhibitors | 박혜영; 권영주 | Article |
2007 | Synthesis of new xanthone analogues and their biological activity test-Cytotoxicity, topoisomerase II inhibition, and DNA cross-linking study | 권영주 | Article |
2014 | Synthesis, antitumor activity, and structure-activity relationship study of trihydroxylated 2,4,6-triphenyl pyridines as potent and selective topoisomerase II inhibitors | 권영주 | Article |
2020 | Synthesis, Biological Evaluation and Molecular Docking Study of Cyclic Diarylheptanoids as Potential Anticancer Therapeutics | 권영주 | Article |
2011 | Synthesis, biological evaluation, and molecular docking study of 3-(3′-heteroatom substituted-2′-hydroxy-1′-propyloxy) xanthone analogues as novel topoisomerase IIα catalytic inhibitor | 박혜영; 권영주 | Article |
2008 | Synthesis, cytotoxicity and topoisomerase II inhibition study of new thioxanthone analogues | 권영주 | Article |
2011 | Synthesis, cytotoxicity and topoisomerase II inhibitory activity of benzonaphthofurandiones | 박혜영; 권영주 | Article |
2007 | Synthesis, cytotoxicity, topoisomerase II inhibition, and DNA cross-linking study of new xanthone analogues | 권영주 | Meeting Abstract |
2010 | Synthesis, topoisomerase i and II inhibitory activities, and cytotoxicity of 4,6-diaryl-2,4'-bipyridine derivatives | 권영주 | Article |
2015 | 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 | 권영주 | Article |
2010 | Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study of hydroxylated 2,4-diphenyl-6-aryl pyridines | 권영주 | Article |
2011 | 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 | 권영주 | Article |
2017 | The Conjugated Double Bond of Coniferyl Aldehyde Is Essential for Heat Shock Factor 1 Mediated Cytotoprotection | 권영주; 이윤실 | Article |
2022 | The Risk of Gastrointestinal Cancer on Daily Intake of Low-Dose BaP in C57BL/6 for 60 Days | 권영주 | Article |
2019 | The synthesis and anticancer activities of chiral epoxy-substituted chromone analogs | 권영주 | Article |
2017 | The synthesis of tamoxifen-loaded albumin nanoparticles by homogenizers: Optimization and in vitro characterization | 권영주 | Article |
2017 | Thiol-reducing agents prevent sulforaphane-induced growth inhibition in ovarian cancer cells | 김승철; 권영주 | Article |
2015 | Topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study of dihydroxylated 2,6-diphenyl-4-aryl pyridines | 권영주 | Article |
2022 | Topoisomerase IIα inhibitory and antiproliferative activity of dihydroxylated 2,6-diphenyl-4-fluorophenylpyridines: Design, synthesis, and structure-activity relationships | 권영주; 황수연 | Article |
2022 | Topologically-Interlocked Minicircles as Probes of DNA Topology and DNA-Protein Interactions | 권영주 | Article |
2016 | Triphenylpyridine Derivatives Inhibit Topoisomerase IIα and Induce Apoptosis in Human Cancer Cells | 신소민 | Master's Thesis |
2005 | Two new diarylheptanoids from Juglans mandshurica | 권영주 | Article |
2019 | Use of saw palmetto (Serenoa repens) extract for benign prostatic hyperplasia | 권영주 | Review |
2015 | Xanthone analogues as potent modulators of intestinal P-glycoprotein | 이화정; 권영주 | Article |
2018 | 에피갈로카테킨 갈레이트의 종양미세환경 제어를 통한 난소암세포 성장 억제 | 박근영 | Master's Thesis |
2017 | 이종이식 마우스 모델을 이용한 커큐민 섭취와 항암치료제의 병용 가능성 평가 | 최보윤 | Master's Thesis |
2023 | 종양미세환경 구성 지방세포가 난소암세포의 이동성에 미치는 영향 | 장아영 | Master's Thesis |
2022 | 종양미세환경이 난소암 세포 성장과 전이에 미치는 영향 | 황경희 | Master's Thesis |
2019 | 한국인의 상용식품 중 캡사이시노이드 함량 데이터베이스 구축 | 조호연 | Master's Thesis |