ANTINEOPLASTIC ACTIVITY;
ARTICLE;
CELL PROLIFERATION;
CONTROLLED STUDY;
DRUG CYTOTOXICITY;
DRUG POTENCY;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
HUMAN;
HUMAN CELL;
IC 50;
IN VITRO STUDY;
MICROTUBULE ASSEMBLY;
MULTIDRUG RESISTANCE;
TUMOR CELL LINE;
ANTINEOPLASTIC AGENTS;
CELL LINE, TUMOR;
CHROMONES;
COLCHICINE;
DRUG RESISTANCE, MULTIPLE;
DRUG RESISTANCE, NEOPLASM;
DRUG SCREENING ASSAYS, ANTITUMOR;
HUMANS;
NAPHTHALENES;
PROTEIN BINDING;
STRUCTURE-ACTIVITY RELATIONSHIP;
THIOPHENES;
TUBULIN;
TUBULIN MODULATORS;
Total synthesis and bioactivity of unique flavone desmosdumotin B and its analogs
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Antitumor agents 260. New desmosdumotin B analogues with improved in vitro anticancer activity
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Antitumor agents. 280. Multidrug resistance-selective desmosdumotin B analogues
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Is resistance useless? Multidrug resistance and collateral sensitivity
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Recent progress in discovery and development of antimitotic agents
Kiselyov, A.; Balakin, K. V.; Tkachenko, S. E.; Savchuk, N.; Ivachtchenko, A. V. Recent progress in discovery and development of antimitotic agents Anti-Cancer Agents Med. Chem. 2007, 7, 189-208 (Pubitemid 46403584)
The mechanism of action of colchicine. Colchicine binding to sea urchin eggs and the mitotic apparatus
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Interactions of tubulin with potent natural and synthetic analogs of the antimitotic agent combretastatin: A structure-activity study
Lin, C. M.; Singh, S. B.; Chu, P. S.; Dempcy, R. O.; Schmidt, J. M.; Pettit, G. R.; Hamel, E. Interactions of tubulin with potent natural and synthetic analogs of the antimitotic agent combretastatin: a structure-activity study Mol. Pharmacol. 1988, 34, 200-208
Naphthalene combretastatin analogues: Synthesis, cytotoxicity and antitubulin activity
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Antitumor agents 259. Design, syntheses, and structure-activity relationship study of desmosdumotin C analogs
DOI 10.1021/jm0702534
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Synthesis and antihemorrhagic activity of 5-methyl-4,7- thionaphthenequinone
Tarbell, D. S.; Fukushima, D. K.; Dam, H. Synthesis and antihemorrhagic activity of 5-methyl-4,7-thionaphthenequinone J. Am. Chem. Soc. 1945, 67, 1643-1644
Preparation and Diels-Alder reactivity of thieno[2,3- c ]- and thieno[3,2- c ]pyran-3-ones, stable 2,3-dimethylenethiophene derivatives; Synthesis of benzothiophenes
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Antitumor Agents. 280. Multidrug resistance-selective desmosdumotin B analogues
Nakagawa-Goto, K.; Chang, P. C.; Lai, C. Y.; Hung, H. Y.; Chen, T. H; Wu, P. C.; Zhu, H.; Sedykh, A.; Bastow, K. F.; Lee, K. H. Antitumor Agents. 280. Multidrug resistance-selective desmosdumotin B analogues J. Med. Chem. 2010, 53, 6699-6705
A common pharmacophore for a diverse set of colchicine site inhibitors using a structure-based approach
DOI 10.1021/jm050502t
Nguyen, T. L.; McGrath, C.; Hermone, A. R.; Burnett, J. C.; Zaharevitz, D. W.; Day, B. W.; Wipf, P.; Hamel, E.; Gussio, R. A common pharmacophores for a diverse set of colchicines site inhibitors using a structure-based approach J. Med. Chem. 2005, 48, 6107-6116 (Pubitemid 41324618)
Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin
Hamel, E. Evaluation of antimitotic agents by quantitative comparisons of their effects on the polymerization of purified tubulin Cell Biochem. Biophys. 2003, 38, 1-22
Structure-activity analysis of the interaction of curacin A, the potent colchicine site antimitotic agent, with tubulin and effects of analogs on the growth of MCF-7 breast cancer cells
Verdier-Pinard, P.; Lai, J. Y.; Yoo, H. D.; Yu, J.; Márquez, B.; Nagle, D. G.; Nambu, M.; White, J. D.; Falck, J. R.; Gerwick, W. H.; Day, B. W.; Hamel, E. Structure-activity analysis of the interaction of curacin A, the potent colchicine site antimitotic agent, with tubulin and effects of analogs on the growth of MCF-7 breast cancer cells Mol. Pharmacol. 1998, 53, 62-76 (Pubitemid 28068373)
Speriolin is a novel spermatogenic cell-specific centrosomal protein associated with the seventh WD motif of Cdc20
Goto, M.; Eddy, E. M. Speriolin is a novel spermatogenic cell-specific centrosomal protein associated with the seventh WD motif of Cdc20 J. Biol. Chem. 2004, 279, 42128-4238