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Volumn 18, Issue 1, 2010, Pages 377-386
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2-Thienyl-4-furyl-6-aryl pyridine derivatives: Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure-activity relationship study
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Author keywords
2 (5 Chlorothiophen 2 yl) 4 (furan 3 yl); 2 Thienyl 4 furyl 6 aryl pyridine; Cytotoxicity; Topoisomerase I and II
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Indexed keywords
2 (2 CHLOROPHENYL) 4 (FURAN 2 YL) 6 (3 METHYLTHIOPHEN 2 YL)PYRIDINE;
2 (2 CHLOROPHENYL) 6 (5 CHLOROTHIOPHEN 2 YL) 4 (FURAN 3 YL)PYRIDINE;
2 (3 CHLOROPHENYL) 6 (5 CHLOROTHIOPHEN 2 YL) 4 (FURAN 3 YL)PYRIDINE;
2 (4 CHLOROPHENYL) 4 (FURAN 2 YL) 6 (3 METHYLTHIOPHEN 2 YL)PYRIDINE;
2 (4 CHLOROPHENYL) 4 (FURAN 3 YL) 6 (3 METHYLTHIOPHEN 2 YL)PYRIDINE;
2 (4 CHLOROPHENYL) 6 (5 CHLOROTHIOPHEN 2 YL) 4 (FURAN 2 YL)PYRIDINE;
2 (4 CHLOROPHENYL) 6 (5 CHLOROTHIOPHEN 2 YL) 4 (FURAN 3 YL)PYRIDINE;
2 (5 CHLOROTHIOPHEN 2 YL) 4 (FURAN 3 YL) 6 (5 METHYLFURAN 2 YL)PYRIDINE;
2 (5 CHLOROTHIOPHEN 2 YL) 4 (FURAN 3 YL) 6 3 TOLYLPYRIDINE;
2 (5 CHLOROTHIOPHEN 2 YL) 4 (FURAN 3 YL) 6 4 TOLYLPYRIDINE;
2 (5 CHLOROTHIOPHEN 2 YL) 6 (FURAN 2 YL) 4 (FURAN 3 YL)PYRIDINE;
2 (FURAN 2 YL) 4 (FURAN 3 YL) 6 (3 METHYLTHIOPHEN 2 YL)PYRIDINE;
2 THIENYL 4 FURYL 6 ARYL PYRIDINE DERIVATIVE;
4 (5 CHLOROFURAN 2 YL) 2 (3 CHLOROPHENYL) 6 (5 CHLOROTHIOPHEN 2 YL)PYRIDINE;
4 (5 CHLOROFURAN 2 YL) 2 (4 CHLOROPHENYL) 6 (3 METHYLTHIOPHEN 2 YL)PYRIDINE;
4 (5 CHLOROFURAN 2 YL) 2 (4 CHLOROPHENYL) 6 (5 CHLOROTHIOPHEN 2 YL)PYRIDINE;
4 (5 CHLOROFURAN 2 YL) 2 (5 CHLOROTHIOPHEN 2 YL) 6 (FURAN 2 YL) PYRIDINE;
4 (5 CHLOROFURAN 2 YL) 2 (5 CHLOROTHIOPHEN 2 YL) 6 2 TOLYLPYRIDINE;
4 (5 CHLOROFURAN 2 YL) 2 (FURAN 2 YL) 6 (3 METHYLTHIOPHEN 2 YL)PYRIDINE;
4 (5 CHLOROFURAN 2 YL) 6 (3 METHYLTHIOPHEN 2 YL) 2,3' BIPYRIDINE;
6 (5 CHLOROTHIOPHEN 2 YL) 4 (FURAN 3 YL) 2, 2' BIPYRIDINE;
6 (5 CHLOROTHIOPHEN 2 YL) 4 (FURAN 3 YL) 2,3' BIPYRIDINE;
ANTINEOPLASTIC AGENT;
CAMPTOTHECIN;
DNA TOPOISOMERASE;
DNA TOPOISOMERASE (ATP HYDROLYSING);
DNA TOPOISOMERASE INHIBITOR;
DOXORUBICIN;
ETOPOSIDE;
UNCLASSIFIED DRUG;
ARTICLE;
CANCER CELL CULTURE;
CELL STRAIN K 562;
CELL STRAIN MCF 7;
CONTROLLED STUDY;
CYTOTOXICITY;
DRUG ACTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME ACTIVITY;
ENZYME INHIBITION;
HELA CELL;
HUMAN;
HUMAN CELL;
STRUCTURE ACTIVITY RELATION;
ANTINEOPLASTIC AGENTS;
CELL LINE, TUMOR;
CELL PROLIFERATION;
DNA TOPOISOMERASES, TYPE I;
DNA TOPOISOMERASES, TYPE II;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMANS;
INHIBITORY CONCENTRATION 50;
NEOPLASMS;
PYRIMIDINES;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 72049095310
PISSN: 09680896
EISSN: None
Source Type: Journal
DOI: 10.1016/j.bmc.2009.10.049 Document Type: Article |
Times cited : (63)
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References (23)
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