Discovery of substituted N-phenyl nicotinamides as potent inducers of apoptosis using a cell- and caspase-based high throughput screening assay
Cai S.X., Nguyen B., Jia S., Herich J., Guastella J., Reddy S., Tseng B., Drewe J., and Kasibhatla S. Discovery of substituted N-phenyl nicotinamides as potent inducers of apoptosis using a cell- and caspase-based high throughput screening assay. J. Med. Chem. 46 (2003) 2474-2481
Comparison of radiolabeled isatin analogs for imaging apoptosis with positron emission tomography
Chen D.L., Zhou D., Chu W., Herrbrich P.E., Jones L.A., Rothfuss J.M., Engle J.T., Geraci M., Welch M.J., and Mach R.H. Comparison of radiolabeled isatin analogs for imaging apoptosis with positron emission tomography. Nucl. Med. Biol. 36 (2009) 651-658
Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay. 1. Structure-activity relationships of the 4-aryl group
Kemnitzer W., Drewe J., 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., Kasibhatla S., and Cai S.X. Discovery of 4-aryl-4H-chromenes as a 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. 47 (2004) 6299-6310
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
Kemnitzer W., Drewe J., Jiang S., Zhang H., Zhao J., Crogan-Grundy C., Xu L., Lamothe S., Gourdeau H., Denis R., Tseng B., Kasibhatla S., and Cai S.X. 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. J Med. Chem. 50 (2007) 2858-2864
Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high throughput screening assay. 4. Structure-activity relationships of N-alkyl substituted pyrrole fused at the 7,8-positions
Kemnitzer W., Drewe J., Jiang S., Zhang H., Crogan-Grundy C., Labreque D., Bubenick M., Attardo G., Denis R., Lamothe S., Gourdeau H., Tseng B., Kasibhatla S., and Cai S.X. Discovery of 4-aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high throughput screening assay. 4. Structure-activity relationships of N-alkyl substituted pyrrole fused at the 7,8-positions. J. Med. Chem. 51 (2008) 417-423
5-Pyrrolidinylsulfonyl isatins as a potential tool for the molecular imaging of caspases in apoptosis
Kopka K., Faust A., Keul P., Wagner S., Breyholz H.J., Holtke C., Schober O., Schafers M., and Levkau B. 5-Pyrrolidinylsulfonyl isatins as a potential tool for the molecular imaging of caspases in apoptosis. J. Med. Chem. 49 (2006) 6704-6715
Automated measurement of specific activity of radiolabeled ligands during synthesis
Mock B.H., Glick-Wilson B.E., Zheng Q.-H., and DeGrado T.R. Automated measurement of specific activity of radiolabeled ligands during synthesis. J. Label. Compd. Radiopharm. 48 (2005) S224
Fluorinated isatin derivatives. Part 2. New N-substituted 5-pyrrolidinylsulfonyl isatins as potential tools for molecular imaging of caspases in apoptosis
Podichetty A.K., Wagner S., Schroer S., Faust A., Schafers M., Schober O., Kopka K., and Haufe G. Fluorinated isatin derivatives. Part 2. New N-substituted 5-pyrrolidinylsulfonyl isatins as potential tools for molecular imaging of caspases in apoptosis. J. Med. Chem. 52 (2009) 3484-3495
Purification of carbon-11 PET radiotracers from unlabeled precursors by preparative HPLC and SPE
Zheng Q.-H., and Mock B.H. Purification of carbon-11 PET radiotracers from unlabeled precursors by preparative HPLC and SPE. Biomed. Chromatogr. 19 (2005) 671-676