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Biophysical Chemistry|June 6, 2006
Microcalorimetry of interaction of dihydro-imidazo-phenanthridinium (DIP)-based compounds with duplex DNAKevin M Guthrie, Alexis D C Parenty, Louise V Smith, et al.The Journal of Organic Chemistry|September 18, 2004
General one-pot, three-step methodology leading to an extended class of N-heterocyclic cations: spontaneous nucleophilic addition, cyclization, and hydride lossAlexis D C Parenty, Louise V Smith, Alexandra L Pickering, et al.Chembiochem : a European Journal of Chemical Biology|October 13, 2006
Dihydroimidazophenanthridinium (DIP)-based DNA binding agents with tuneable structures and biological activityLouise V Smith, Alexis D C Parenty, Kevin M Guthrie, et al.Chemical Communications (Cambridge, England)|March 7, 2006
Discovery of an imidazo-phenanthridine synthon produced in a 'five-step one-pot reaction' leading to a new family of heterocycles with novel physical propertiesAlexis D C Parenty, Kevin M Guthrie, Yu-Fei Song, et al.Journal of Medicinal Chemistry|July 8, 2005
Highly stable phenanthridinium frameworks as a new class of tunable DNA binding agents with cytotoxic propertiesAlexis D C Parenty, Louise V Smith, Kevin M Guthrie, et al.Chemical Communications (Cambridge, England)|June 21, 2007
Incorporation of N-heterocyclic cations into proteins with a highly directed chemical modificationNicola McMillan, Louise V Smith, Jesus M de la Fuente, et al.Pageof 1