Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 3. Structure-activity relationships of fused rings at the 7,8-positions
APOPTOSIS;
ARTICLE;
CANCER CELL;
CANCER INHIBITION;
CELL PROLIFERATION;
CONTROLLED STUDY;
DRUG MECHANISM;
DRUG STRUCTURE;
HIGH THROUGHPUT SCREENING;
HUMAN;
HUMAN CELL;
MICROTUBULE ASSEMBLY;
STRUCTURE ACTIVITY RELATION;
ANTINEOPLASTIC AGENTS;
APOPTOSIS;
BENZOPYRANS;
CASPASES;
CELL PROLIFERATION;
DRUG SCREENING ASSAYS, ANTITUMOR;
ENZYME ACTIVATION;
HETEROCYCLIC COMPOUNDS WITH 4 OR MORE RINGS;
HUMANS;
INDOLES;
STRUCTURE-ACTIVITY RELATIONSHIP;
Tubulin as a target for anticancer drugs: Agents which interact with the mitotic spindle
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Dissecting cellular processes using small molecules: Identification of colchicine-like, Taxol-like and other small molecules that perturb mitosis
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A chemical genetics approach for the discovery of apoptosis inducers: From phenotypic cell based HTS assay and structure-activity relationship studies, to identification of potential anticancer agents and molecular targets
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Kemnitzer, W.; Kasibhatla, S.; Jiang, S.; Zhang, H.; Wang, Y.; Zhao, J.; Jia, S.; Herich, J.; Labreque, D.; Storer, R.; Meerovitch, K.; Bouffard, D.; Rej, R.; Denis, R.; Blais, C.; Lamothe, S.; Attardo, G.; Gourdeau, H.; Tseng, B.; Drewe, J.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as new series of apoptosis inducers using a cell-and caspase-based high-throughput screening assay. 1. Structure-activity relationships of the 4-aryl group. J. Med. Chem. 2004, 47, 6299-6310.
Kemnitzer, W.; Kasibhatla, S.; Jiang, S.; Zhang, H.; Wang, Y.; Zhao, J.; Jia, S.; Herich, J.; Labreque, D.; Storer, R.; Meerovitch, K.; Bouffard, D.; Rej, R.; Denis, R.; Blais, C.; Lamothe, S.; Attardo, G.; Gourdeau, H.; Tseng, B.; Drewe, J.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as new series of apoptosis inducers using a cell-and caspase-based high-throughput screening assay. 1. Structure-activity relationships of the 4-aryl group. J. Med. Chem. 2004, 47, 6299-6310.
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Kemnitzer, W.; Kasibhatla, S.; Jiang, S.; Zhang, H.; Zhao, J.; Jia, S.; Xu, L.; Crogan-Grundy, C.; Denis, R.; Barriault, N.; Vaillancourt, L.; Charron, S.; Dodd, J.; Attardo, G; Labrecque, D.; Lamothe, S.; Gourdeau, H.; Tseng, B.; Drewe, J.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 2. Structure-activity relationships of the 7- and 5-, 6-, 8-positions. Bioorg. Med. Chem. Lett. 2005, 15, 4745-4751.
Kemnitzer, W.; Kasibhatla, S.; Jiang, S.; Zhang, H.; Zhao, J.; Jia, S.; Xu, L.; Crogan-Grundy, C.; Denis, R.; Barriault, N.; Vaillancourt, L.; Charron, S.; Dodd, J.; Attardo, G; Labrecque, D.; Lamothe, S.; Gourdeau, H.; Tseng, B.; Drewe, J.; Cai, S. X. Discovery of 4-aryl-4H-chromenes as new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 2. Structure-activity relationships of the 7- and 5-, 6-, 8-positions. Bioorg. Med. Chem. Lett. 2005, 15, 4745-4751.
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Discovery of substituted 4-anilino-2-(2-pyridyl)pyrimidines as a new series of apoptosis inducers using a cell- and caspase-based high throughput screening assay. Part 1: Structure-activity relationships of the 4-anilino group
Sirisoma, N.; Kasibhatla, S.; Nguyen, B.; Pervin, A.; Wang, Y.; Claassen, G.; Tseng, B.; Drewe, J.; Cai, S. X. Discovery of substituted 4-anilino-2-(2-pyridyl)pyrimidines as a new series of apoptosis inducers using a cell- and caspase-based high throughput screening assay. Part 1: Structure-activity relationships of the 4-anilino group. Bioorg. Med. Chem. 2006, 14, 7761-7773.
Discovery and SAR of indole-2-carboxylic acid benzylidenehydrazides as a new series of potent apoptosis inducers using a cell based HTS assay
Zhang, H.; Drewe, J.; Tseng, B.; Kasibhatla, S.; Cai, S. X. Discovery and SAR of indole-2-carboxylic acid benzylidenehydrazides as a new series of potent apoptosis inducers using a cell based HTS assay. Bioorg. Med. Chem. 2004, 12, 3649-3655.