Authors: Tercel, M Lee, AE Hogg, A Anderson, RF Lee, HH Siim, BG Denny, WA Wilson, WR

Citation: M. Tercel et al., Hypoxia-selective antitumor agents. 16. Nitroarylmethyl quaternary salts as bioreductive prodrugs of the alkylating agent mechlorethamine, J MED CHEM, 44(21), 2001, pp. 3511-3522

Authors: Tercel, M Gieseg, MA Milbank, JB Boyd, M Fan, JY Tan, LK Wilson, WR Denny, WA

Citation: M. Tercel et al., Cytotoxicity and DNA Interaction of the enantiomers of 6-amino-3-(chloromethyl)-1-[(5,6,7-trimethoxyindol-2-yl)-carbonyl]indoline (amino-seco-CI-TMI), CHEM RES T, 12(8), 1999, pp. 700-706

Authors: Tercel, M Gieseg, MA Denny, WA Wilson, WR

Citation: M. Tercel et al., Synthesis and cytotoxicity of amino-seco-DSA: An amino analogue of the DNAalkylating agent duocarmycin SA, J ORG CHEM, 64(16), 1999, pp. 5946-5953

Authors: Milbank, JBJ Tercel, M Atwell, GJ Wilson, WR Hogg, A Denny, WA

Citation: Jbj. Milbank et al., Synthesis of 1-substituted 3-(chloromethyl)-6-aminoindoline (6-amino-seco-CI) DNA minor groove alkylating agents and structure-activity relationshipsfor their cytotoxicity, J MED CHEM, 42(4), 1999, pp. 649-658

Authors: Wilson, WR Tercel, M Anderson, RF Denny, WA

Citation: Wr. Wilson et al., Radiation-activated prodrugs as hypoxia-selective cytotoxins: model studies with nitroarylmethyl quaternary salts, ANTI-CAN DR, 13(6), 1998, pp. 663-685

Authors: Atwell, GJ Tercel, M Boyd, M Wilson, WR Denny, WA

Citation: Gj. Atwell et al., Synthesis and cytotoxicity of 5-amino-1-(chloromethyl)-3-[(5,6,7-trimethoxyindol-2-yl)carbonyl]-1,2-dihydro-3H-benz[e]indole (amino-seco-CBI-TMI) andrelated 5-alkylamino analogues: New DNA minor groove alkylating agents, J ORG CHEM, 63(25), 1998, pp. 9414-9420