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Publisher: Cognizant Communication Corporation

Volume 16, Number 1, 2001

A prodrug approach to the design of cRaf1 kinase inhibitors with improved cellular activity
pp. 1-6(6)
Authors: Wood, Edgar; Crosby, Renae M.; Dickerson, Scott; Frye, Stephen V.; Griffin, Robert; Hunter, Robert; Jung, David K.; McDonald, O. Bradley; McNutt, Robert; Mahony, William B.; Peel, Michael R.; Ray, John

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Cell‐based screening approach for antitumor drug leads which exploits sensitivity differences between normal and cancer cells: identification of two novel cell‐cycle inhibitors
pp. 7-17(11)
Authors: Vassilev, Lyubomir T.; Kazmer, Sonja; Marks, Ian M.; Pezzoni, Gabriella; Sala, Franca; Mischke, Steven G.; Foley, Louise

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A novel B‐ring modified homocamptothecin, 12‐Cl‐hCPT, showing antiproliferative and topoisomerase I inhibitory activities superior to SN‐38
pp. 27-36(10)
Authors: Bailly, Christian; Laine, William; Baldeyrou, Brigitte; Demarquay, Danièle; Huchet, Marion; Coulomb, Hélène; Lanco, Christophe; Lavergne, Olivier

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Synthesis, evaluation and QSAR studies of highly potent aromatase inhibitors of the piperidinedione type
pp. 37-47(11)
Authors: Baston, Eckhard; Klein, Christian D.P.; Grimminger, Wolf; Hebecker, Norbert

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Synthesis and anti‐melanoma activity of analogues of N‐acetyl‐4‐S‐cysteaminylphenol substituted with two methyl groups α to the nitrogen
pp. 49-55(7)
Authors: Lant, Neil J.; McKeown, Paul; Timoney, Maire C.; Kelland, Lloyd R.; Rogers, Paul M.

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Erratum
pp. 71-71(1)

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