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Mutation Research|October 1, 1990
Structure-activity relationships for the mutagenic activity of tricyclic intercalating agents in Salmonella typhimuriumW A Denny, P M Turner, G J Atwell, et al.Anti-Cancer Drug Design|October 1, 1992
Structure-activity relationships for substituted 9-oxo-9,10-dihydroacridine-4-acetic acids: analogues of the colon tumour active agent xanthenone-4-acetic acidS A Gamage, G W Rewcastle, G J Atwell, et al.Journal of Medicinal Chemistry|April 1, 1988
Potential antitumor agents. 54. Chromophore requirements for in vivo antitumor activity among the general class of linear tricyclic carboxamidesB D Palmer, G W Rewcastle, G J Atwell, et al.Journal of Medicinal Chemistry|April 1, 1989
Potential antitumor agents. 58. Synthesis and structure-activity relationships of substituted xanthenone-4-acetic acids active against the colon 38 tumor in vivoG W Rewcastle, G J Atwell, B C Baguley, et al.Journal of Medicinal Chemistry|September 1, 1986
Potential antitumor agents. 47. 3'-Methylamino analogues of amsacrine with in vivo solid tumor activityG J Atwell, B C Baguley, G J Finlay, et al.Journal of Medicinal Chemistry|March 3, 1999
Synthesis of 1-substituted 3-(chloromethyl)-6-aminoindoline (6-amino-seco-CI) DNA minor groove alkylating agents and structure-activity relationships for their cytotoxicityJ B Milbank, M Tercel, G J Atwell, et al.Journal of Medicinal Chemistry|February 13, 1999
N-Substituted 2-(2,6-dinitrophenylamino)propanamides: novel prodrugs that release a primary amine via nitroreduction and intramolecular cyclizationB M Sykes, G J Atwell, A Hogg, et al.Journal of Medicinal Chemistry|July 8, 1994
Hypoxia-selective antitumor agents. 9. Structure-activity relationships for hypoxia-selective cytotoxicity among analogues of 5-[N,N-bis(2-chloroethyl)amino]-2,4-dinitrobenzamideB D Palmer, W R Wilson, G J Atwell, et al.Anti-Cancer Drug Design|September 29, 1999
Dimeric analogues of non-cationic tricyclic aromatic carboxamides are a new class of cytotoxic agentsJ A Spicer, S A Gamage, G J Atwell, et al.Journal of Medicinal Chemistry|June 6, 1997
Structure-activity relationships for acridine-substituted analogues of the mixed topoisomerase I/II inhibitor N-[2-(dimethylamino)ethyl]acridine-4-carboxamideJ A Spicer, S A Gamage, G J Atwell, et al.Pageof 7