2,4-Diaryl-5,6-dihydro-1,10-phenanthrolines with Furyl or Thienyl Moiety at 4-Position: Synthesis, Topoisomerase I and II Inhibitory Activity, and Cytotoxicity

Eung-Seok Lee; Pritam Thapa

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2,4-Diaryl-5,6-dihydro-1,10-phenanthrolines with Furyl or Thienyl Moiety at 4-Position: Synthesis, Topoisomerase I and II Inhibitory Activity, and Cytotoxicity

机译：具有4-位呋喃基或噻吩基部分的2,4-二芳基-5,6-二氢-1,10-菲咯啉：合成，拓扑异构酶I和II抑制活性和细胞毒性

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《Bulletin of the Korean Chemical Society》 |2012年第5期|共页
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Eung-Seok Lee; Pritam Thapa;
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1. 2,4-Diaryl-5,6-dihydro-1,10-phenanthrolines with Furyl or Thienyl Moiety at 4-Position: Synthesis, Topoisonierase I and II Inhibitory Activity, and Cytotoxicity [J] . Pritam Thapa, Eung-Seok Lee Bulletin of the Korean Chemical Society . 2012,第5期

机译：具有4-位呋喃基或噻吩基部分的2,4-二芳基-5,6-二氢-1,10-菲咯啉：合成，拓扑黄酮酶I和II的抑制活性和细胞毒性
2. 2-Thienyl-4-furyl-6-aryl pyridine derivatives: synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study. [J] . Thapa P, Karki R, Thapa Bioorganic and medicinal chemistry . 2010,第1期

机译：2-噻吩-4-呋喃基-6-芳基吡啶衍生物：合成，拓扑异构酶I和II抑制活性，细胞毒性和结构活性关系的研究。
3. 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. [J] . Thapa P, Karki R, Choi H, Bioorganic and medicinal chemistry . 2010,第6期

机译：2-（噻吩基-2-基或-3-基）-4-呋喃基-6-芳基吡啶衍生物的合成及其拓扑异构酶I和II的抑制活性，细胞毒性和结构活性关系的评估。
4. Synthesis and Property of a New 2,4-position Hybrid Diarylethene Bearing both Benzene and Isoxazole Moieties [C] . Hui Li, Shouzhi Pu, Gang Liu, ICAMCS 2011;International conference on advanced materials and computer science . 2012

机译：新型的同时带有苯和异恶唑基团的2,4-位杂二芳基乙烯的合成和性能
5. Reactivity of sigma-thienyl, sigma-indolyl and sigma-furyl ligands at ditungsten and dimolybdenum centers 'relevance toward HDS, HDN and HDO' [D] . Haubrich, Scott Thomas 1995

机译：σ-噻吩基，σ-吲哚基和σ-呋喃基配体在钨和二钼中心的反应性“与HDS，HDN和HDO的相关性”
6. Pharmacophore-based virtual screening synthesis biological evaluation and molecular docking study of novel pyrrolizines bearing urea/thiourea moieties with potential cytotoxicity and CDK inhibitory activities [O] . Ahmed M. Shawky, Nashwa A. Ibrahim, Mohammed A. S. Abourehab, 2021

机译：基于药疗法的虚拟筛选合成生物评价和具有潜在细胞毒性和CDK抑制活动的新型吡咯嗪的含脲/硫脲部分的分子对接研究
7. Synthesis of 2,4,6-Tripyridyl Pyridines, and Evaluation of Their Antitumor Cytotoxicity, Topoisomerase I and II Inhibitory Activity, and Structure-activity Relationship [O] . Byeong-Seon Jeong, Ho-Young Choi, Young-Shin Kwak, 2011

机译：合成2,4,6-三吡啶吡啶，评价其抗肿瘤细胞毒性，拓扑异构酶I和II抑制活性，以及结构 - 活性关系

2,4-Diaryl-5,6-dihydro-1,10-phenanthrolines with Furyl or Thienyl Moiety at 4-Position: Synthesis, Topoisomerase I and II Inhibitory Activity, and Cytotoxicity

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