Novel quinolinequinone antitumor agents: structure-metabolism studies with NAD (P) H: quinone oxidoreductase (NQO1)
T Fryatt, DT Goroski, ZD Nilson, CJ Moody…
Index: Fryatt, Tara; Goroski, Dean T.; Nilson, Zachary D.; Moody, Christopher J.; Beall, Howard D. Bioorganic and Medicinal Chemistry Letters, 1999 , vol. 9, # 15 p. 2195 - 2198
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Citation Number: 33
Abstract
The effects of functional group changes on the metabolism of novel quinolinequinones by recombinant human NAD (P) H: quinone oxidoreductase (NQO1) are described. Overall, the quinolinequinones were much better substrates for NQO1 than analogous indolequinones, with compounds containing heterocyclic substituents at C-2 being among the best substrates.
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[Fryatt, Tara; Pettersson, Hanna I.; Gardipee, Walter T.; Bray, Kurtis C.; Green, Stephen J.; Slawin, Alexandra M. Z.; Beall, Howard D.; Moody, Christopher J. Bioorganic and Medicinal Chemistry, 2004 , vol. 12, # 7 p. 1667 - 1687]
[Fryatt, Tara; Pettersson, Hanna I.; Gardipee, Walter T.; Bray, Kurtis C.; Green, Stephen J.; Slawin, Alexandra M. Z.; Beall, Howard D.; Moody, Christopher J. Bioorganic and Medicinal Chemistry, 2004 , vol. 12, # 7 p. 1667 - 1687]
[Fryatt, Tara; Pettersson, Hanna I.; Gardipee, Walter T.; Bray, Kurtis C.; Green, Stephen J.; Slawin, Alexandra M. Z.; Beall, Howard D.; Moody, Christopher J. Bioorganic and Medicinal Chemistry, 2004 , vol. 12, # 7 p. 1667 - 1687]
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