ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CYTOTOXICITY;
DRUG BINDING;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME INHIBITION;
HUMAN;
HUMAN CELL;
MOLECULAR INTERACTION;
STRUCTURE ACTIVITY RELATION;
ANTINEOPLASTIC AGENTS;
AZA COMPOUNDS;
CELL LINE, TUMOR;
DNA;
DNA CLEAVAGE;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMANS;
INDENES;
ISOQUINOLINES;
MODELS, MOLECULAR;
QUANTUM THEORY;
STRUCTURE-ACTIVITY RELATIONSHIP;
THERMODYNAMICS;
TOPOISOMERASE I INHIBITORS;
Protein-linked DNA strand breaks induced by NSC 314622, a novel noncamptothecin topoisomerase I poison
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Synthesis and mechanism of action studies of a series of norindenoisoquinoline topoisomerase I poisons reveal an inhibitor with a flipped orientation in the ternary DNA-enzyme-inhibitor complex as determined by X-ray crystallographic analysis
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Cushman, M.; Ioanoviciu, A.; Antony, S.; Pommier, Y.; Staker, B. L.; Stewart, L. Synthesis and Mechanism of Action Studies of a Series of Norindenoisoquinoline Topoisomerase I Poisons Reveal an Inhibitor with a Flipped Orientation in the Ternary DNA-Enzyme-Inhibitor Complex As Determined by X-ray Crystallographic Analysis J. Med. Chem. 2005, 48, 4803-4814 (Pubitemid 41033123)
Structures of three classes of anticancer agents bound to the human topoisomerase I-DNA covalent complex
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Synthesis and evaluation of indenoisoquinoline topoisomerase I inhibitors substituted with nitrogen heterocycles
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Novel indenoisoquinolines NSC 725776 and NSC 724998 produce persistent topoisomerase I cleavage complexes and overcome multidrug resistance
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Synthesis of New Indeno[1,2- c ]isoquinolines: Cytotoxic Non-Camptothecin Topoisomerase i Inhibitors
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Investigation of the lactam side chain length necessary for optimal indenoisoquinoline topoisomerase I inhibition and cytotoxicity in human cancer cell cultures
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Nitrated indenoisoquinolines as topoisomerase I inhibitors: A systematic study and optimization
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Morrell, A.; Placzek, M.; Parmley, S.; Antony, S.; Dexheimer, T. S.; Pommier, Y.; Cushman, M. Nitrated Indenoisoquinolines as Topoisomerase I Inhibitors: A Systematic Study and Optimization J. Med. Chem. 2007, 50, 4419-4430 (Pubitemid 47378839)
A systematic study of nitrated indenoisoquinolines reveals a potent topoisomerase I inhibitor
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Optimization of the indenone ring of indenoisoquinoline topoisomerase I inhibitors
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7-Azaindenoisoquinolines as Topoisomerase i Inhibitors and Potential Anticancer Agents
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Facile and convenient syntheses of 6,11-dihydro-5H-indeno[1,2-c] isoquinolin-5-ones and 6,11-dihydro-5H-indolo[3,2-c]isoquinolin-5-one
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Asymmetric Hydrogenation of Pyridines: Enantioselective Synthesis of Nipecotic Acid Derivatives
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Studies on anticoccidial agents. 12. Synthesis and anticoccidial activity of methyl-2(6)-nitro- and -3(5)-nitropyridinecarboxamides
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A facile nuclear bromination of phenols and anilines using NBS in the presence of ammonium acetate as a catalyst
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Stille-Type Cross-Coupling-An Efficient Way to Various Symmetrically and Unsymmetrically Substituted Methyl-Bipyridines: Toward New ATRP Catalysts
Schubert, U. S.; Eschbaumer, C.; Heller, M. Stille-Type Cross-Coupling-An Efficient Way to Various Symmetrically and Unsymmetrically Substituted Methyl-Bipyridines: Toward New ATRP Catalysts Org. Lett. 2000, 2, 3373-3376
Acridone-based inhibitors of inosine 5′-monophosphate dehydrogenase: Discovery and SAR leading to the identification of N-(2-(6-(4-ethylpiperazin-1- yl)pyridin-3-yl)propan-2-yl)-2-fluoro-9-oxo-9,10- dihydroacridine-3-carboxamide (BMS-566419)
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The Binding Orientation of a Norindenoisoquinoline in the Topoisomerase I-DNA Cleavage Complex Is Primarily Governed by π-π Stacking Interactions
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On the binding of indeno[1,2-c]isoquinolines in the DNA-topoisomerase I cleavage complex
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An ab initio quantum mechanics calculation that correlates with ligand orientation and DNA cleavage site selectivity in camptothecin-DNA-topoisomerase I ternary cleavage complexes
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Xiao, X. S.; Cushman, M. An Ab Initio Quantum Mechanics Calculation That Correlates With Ligand Orientation and DNA Cleavage Site Selectivity in Camptothecin-DNA-Topoisomerase I Ternary Cleavage Complexes J. Am. Chem. Soc. 2005, 127, 9960-9961 (Pubitemid 40995415)
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Selective cyclooxygenase-2 inhibitors: Heteroaryl modified 1,2-diarylimidazoles are potent, orally active antiinflammatory agents
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Analogues of 1-(3,10-Dibromo-8-chloro-6,11-dihydro-5H-benzo[5,6]- cyclohepta[1, 2-b]pyridin-11-yl)piperidine as inhibitors of farnesyl protein transferase
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Induction of reversible complexes between eukaryotic DNA topoisomerase I and DNA-containing oxidative base damages: 7,8-dihydro-8-oxoguanine and 5- hydroxycytosine
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